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Systematic Review of Self-Assessment Scales for Negative Symptoms in Schizophrenia

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17 December 2024

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18 December 2024

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Abstract
Background/Objectives: Negative symptoms (NS) significantly impair the outcome of schizophrenia, primarily due to their effect on quality of life and their resistance to pharmacological treatments. Several scales have been developed to assess the various dimensions of NS, including avolition, anhedonia, alogia, social withdrawal, and blunted affect. While observer-rated scales are the most commonly used, self-assessment tools remain underutilized. However, self-assessments offer a promising approach for gaining insights into the personal experiences of individuals. The objective of this review was to identify and report the psychometric properties of self-assessment scales for NS that are relevant for both research and clinical practice, with a focus on tools that assess multiple domains of NS in order to support comprehensive evaluations and tailored therapeutic strategies. Methods: We conducted an exhaustive literature review following PRISMA guidelines to identify self-evaluation scales that evaluate several domains of NS in the MEDLINE and Web of Science databases. The COSMIN checklist was used to assess the methodological quality of each tool. Results: Our review identified 5 self-assessment scales. Among these, two scales received a Grade A recommendation for use in clinical or research practice: the Self-evaluation Negative Symptom (SNS), which assesses the five domains of NS, and the Motivation And Pleasure Scale Self-report (MAP-SR), which evaluates anhedonia, avolition, and social withdrawal. Conclusions: The SNS and the MAP-SR are the only tools with sufficient psychometric properties, making them reliable for use in both research and clinical practice. Despite the development of self-assessment tools for NS, their integration into research and clinical settings remains limited, highlighting the need for increased utilization to enhance the understanding and management of these symptoms.
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1. Introduction

Schizophrenia is a complex psychiatric disorder with various symptoms, the most disabling of which are negative symptoms (NS). NS are categorized into five dimensions: anhedonia, avolition, blunted affect, social withdrawal, and alogia [1]. Early detection and continuous monitoring of NS are crucial for developing optimal and personalized treatment strategies. NS significantly impact the progression of the disease due to their high prevalence [2], their effect on daily life [3], and their resistance to treatments [4].
Several scales have been developed to assess NS in patients with schizophrenia, most of which rely on observer ratings [5], and several papers have reported their psychometric properties [6,7,8]. These tools require clinical interviews with trained psychiatrists and are not suitable for evaluating patients' subjective experiences. The integration of self-assessment scales for evaluating symptomatology has emerged as a promising approach for understanding and managing psychotic disorders. Patients’ self-assessments can provide insights into their own experiences that may not be detected by clinicians during interviews [9,10]. By placing patients at the center of their care, these tools can improve awareness and understanding of the illness, thereby increasing engagement in treatment and empowering patients[11]. Additionally, self-assessments are particularly useful for the early detection of psychotic symptoms [12].
The European Psychiatric Association recommends combining hetero-evaluation tools, such as the Brief Negative Syndrome Scale (BNSS) [13] or the Clinical Assessment Interview for Negative Symptoms (CAINS) [14], with self-assessment scales, such as the Self-evaluation of Negative Symptoms (SNS) [15] or the Motivation And Pleasure-Self Report (MAP-SR) [16,17]. These recommendations emphasize the need for a comprehensive approach to assessing NS that considers both clinician-rated and self-reported measures across the five relevant dimensions. Along these lines, new self-report tools have been developed, but paradoxically, they are underused in clinical practice and research. Some of these tools assess only a single dimension of NS, which limits their clinical utility. While specialized tools targeting specific dimensions, such as motivation or anhedonia, are valuable for focused research or interventions [18], they do not provide a complete picture of NS [19]. Given that NS are complex and multifactorial, an effective evaluation tool must consider the interplay between multiple dimensions to guide clinical decision-making. Therefore, this review focuses on self-assessment scales that evaluate multiple domains of NS. The aim is to identify the most relevant tools for clinical practice and research by evaluating their psychometric properties to ensure a comprehensive assessment of NS.

2. Materials and Methods

Data for this systematic review were collected in accordance with the Systematic Reviews and Meta-Analyses guidelines [PRISMA] (Table A1) [20]. This review was not pre-registered.

2.1. COSMIN Methodology

The Consensus-based Standards for the Selection of health Measurement Instruments (COSMIN) checklist was used to ensure a rigorous evaluation of the methodological quality of each self-assessment scale included in this review [21,22,23]. COSMIN methodology was chosen for its structured approach to assessing the psychometric quality of measurement tools. The COSMIN steps involved in this study were: conducting a comprehensive literature search, utilizing the Risk of Bias checklist, applying updated criteria for good measurement properties, implementing the GRADE approach to evaluate evidence quality, and developing evidence-based recommendations.

2.2. Search Method

A systematic electronic search was conducted in the MEDLINE and Web of Science databases. The following search query was used, incorporating the names of tools identified in a previous review [5]:
"Psychometric validation AND (self-report scale OR self-assessment scale OR Self-Evaluation of Deficit Syndrome OR SEDS OR Subjective Experience of Negative Symptoms OR SENS OR Motivation And Pleasure Scale Self-report OR MAP-SR OR Self-evaluation of Negative Symptoms OR SNS) AND (negative symptoms OR anhedonia OR avolition OR motivation OR social withdrawal OR blunted affect OR alogia) AND (psychotic disorders OR schizophrenia OR schizoaffective disorder OR first-episode psychosis OR ultra-high risk of psychosis OR FEP OR UHR)".
Inclusion criteria encompassed studies published in English or French from 1987 to November 2024 that evaluated the psychometric properties of self-assessment tools specifically developed to detect or assess NS in psychotic disorders, including schizophrenia, schizoaffective disorder, first-episode psychosis, and ultra-high risk of psychosis. Exclusion criteria included studies on other disorders, meta-analyses or literature reviews, studies not reporting the psychometric characteristics of the clinical tools, studies not focusing on self-assessment scales or on NS, and tools focused specifically on only one domain of NS (Figure 1).
Although meta-analyses and literature reviews were excluded from the electronic search, a manual search of their bibliographies was conducted to identify additional validation studies for self-assessment tools not initially included. Data were extracted and analyzed by one author (LM).
For each tool, details regarding the population (number, age, gender), number of items, psychometric properties, countries of validation, and negative dimensions were documented.

2.3. Assessing the Risk of Bias and Updated Criteria for Good Measurement Properties

The COSMIN methodology [21,22,23] was applied to evaluate both the risk of bias and the measurement properties of the self-assessment tools for NS.
In this review, we focused on the following psychometric properties: internal consistency (via Cronbach’s alpha, contingent on evidence of structural validity), test-retest reliability (evaluated using the intraclass correlation coefficient (ICC)), structural validity (analyzed through factor analysis), criterion validity (evaluated by Area Under Receiver Operating Characteristic Curve (AUROC) analysis), and hypothesis testing for construct validity based on convergent and discriminant validity (ensuring predefined hypotheses were tested). Finally, responsiveness was excluded due to the absence of a true gold standard measure for the self-assessment of negative symptoms, and cross-cultural validity/measurement invariance were not assessed, as they were addressed in only one study [24].
Initially, we utilized the COSMIN Risk of Bias Checklist, where each measurement property was rated on a four-point scale (“very good”,” adequate”, ”doubtful”, “inadequate”, or “not applicable”). When several studies were identified assessing a psychometric property, the "worst score counts" rule was applied, meaning that the overall rating was the lowest score. The second phase assessed the measurement properties according to the updated COSMIN criteria, with each property rated as “sufficient” (+), “insufficient” (−), or “indeterminate” (?). The “indeterminate” rating was assigned when the data were insufficient for a conclusive assessment.

2.4. GRADE Approach

The Grading of Recommendations Assessment, Development, and Evaluation (GRADE) focuses on the confidence in the quality of evidence [21,22,23]. This approach evaluates evidence quality based on four factors: (1) risk of bias, assessing the methodological quality of studies; (2) inconsistency, referring to unexplained variations in results across studies; (3) imprecision, considering the total sample size of the available studies; and (4) indirectness, indicating whether the evidence comes from populations different from the one targeted in the review. Each factor allows for downgrading by one or more levels, and downgrades can be cumulative across the four criteria. The last criterion was not considered in the present study, as the studies were selected based on specific populations.
The process begins with the assumption that the result is of high quality. However, if the findings are deemed insufficient, the quality may be downgraded, resulting in the categorization of evidence quality as “high”, “moderate”, “low”, or “very low”.
From the assessment of the “risk of bias”, only the studies that received a “+” or “−” rating based on the updated criteria for good measurement were considered for downgrading the confidence in the evidence. Downgrades were applied as follows:
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No downgrade: Multiple studies of at least adequate quality, or a single study of very good quality available
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- 1 downgrade -serious risk of bias: Multiple studies of doubtful quality available, or only one study of adequate quality
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- 2 downgrades-very serious risk of bias: Multiple studies of inadequate quality, or only one study of doubtful quality available
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- 3 downgrades - extremely serious risk of bias: Only one study of inadequate quality available.
Regarding “inconsistency”, the criteria for downgrading were established as follows: the rating on the scale remained unchanged if no inconsistency, or only minimal inconsistency with a valid explanation, was observed. Conversely, if minor inconsistency was found without any explanation, or if moderate to high inconsistency occurred with a valid justification, the rating on the scale was downgraded by one level (serious). In instances of moderate to high inconsistency without a satisfactory explanation, a downgrade of two levels (very serious) was applied.
For “imprecision”, the total sample size of all the studies was considered, with a downgrade of one level for sample sizes between 50 and 100, and a downgrade of two levels for sample sizes smaller than 50.
Research manuscripts reporting large datasets that are deposited in a publicly available database should specify where the data have been deposited and provide the relevant accession numbers. If the accession numbers have not yet been obtained at the time of submission, please state that they will be provided during review. They must be provided prior to publication.
Interventionary studies involving animals or humans, and other studies that require ethical approval, must list the authority that provided approval and the corresponding ethical approval code.

2.5. Recommendations

Using the information from the previous section, COSMIN recommendations [21,22,23] for the level of evidence of the different self-assessment scales are formulated as follows:
A. Sufficient content validity evidence (of any level) and at least low-quality evidence for adequate internal consistency.
B. This category includes studies that do not qualify for either category A or C. It encompasses those with inadequate results, such as missing information on specific measurement properties, preventing classification into either category.
C. High-quality evidence demonstrating an insufficient measurement property.
This classification framework serves as a guide for recommendations on the clinical use and application of these scales.

3. Results

Twenty-six articles related to 5 self-assessment scales were analyzed, covering several NS domains. Table 1 provides the following information about the scales. The COSMIN quality criteria for good measurement, the risk of bias, the Grade evaluation, and recommendation are outlined in Table 2.

3.1. The Subjective Experience of Negative Symptoms (SENS)

The Subjective Experience of Negative Symptoms (SENS) [25] assesses “affective flattening,” “alogia,” “avolition-apathy,” “anhedonia-asociality,” and “attention” through 21 items.

3.1.1. Risk of Bias and Criteria for Good Measurement Properties

Only one study [25] evaluated the psychometric properties of the SENS, focusing solely on internal consistency and reliability. The risk of bias regarding internal consistency was rated as “doubtful” due to a lack of information regarding the scale’s structural validity, which led to the measurement properties being rated as “indeterminate”.
Regarding reliability, the risk of bias was assessed as “adequate”, but the overall evaluation of the measurement properties was “negative” due to the ICC being under 0.70.

3.1.2. GRADE Evaluation

Insufficient findings led to a downgrade of -1. Since there was only one study of adequate quality assessing reliability, this resulted in a serious risk of bias and an additional downgrade of -1
The criterion for inconsistency was not applicable, as there was only one validation study.
For imprecision, as the sample size was n = 52, an additional downgrade of -1 was applied, resulting in a “very low” grade for the SENS.
Thus, the overall quality of the evidence for the SENS scale was considered “very low”, and the level of recommendation was C.

3.2. The Clinical Assessment Interview for Negative Symptoms – Self-Report (CAINS-SR)

The Clinical Assessment Interview for Negative Symptoms – Self-Report (CAINS-SR) [26] is a 30-item self-report measure based on the CAINS interview version, which evaluates the five domains of NS.

3.2.1. Risk of Bias and Criteria for Good Measurement Properties

Only one study [26] examined the psychometric properties of the CAINS-SR, focusing on internal consistency and testing hypotheses for construct convergent and discriminant validity.
The risk of bias for internal consistency was rated as "doubtful" due to limited information on the scale's structural validity, leading to an “indeterminate” assessment of the measurement properties.
For hypothesis testing of both convergent and discriminant validity, the risk of bias was considered “adequate”, and the measurement properties were rated “positive”. The “experience” and “motivation” dimensions of the CAINS-SR were compared with the corresponding dimensions rated by clinicians on the CAINS [14] for convergent validity, as well as with the “positive”, “agitation/mania”, and “depression/anxiety” dimensions of the Brief Psychiatric Rating Scale (BPRS)[27] for discriminant validity.

3.2.2. GRADE Evaluation

As the findings were insufficient, a downgrade of -1 was applied. Since there was only one study of adequate quality, this led to a serious risk of bias and an additional downgrade of -1.
The criterion for inconsistency was not applicable, as only one validation study was available.
For imprecision, the sample size was n = 73, which led to an additional downgrade of -1.
Thus, the overall quality of the evidence for the CAINS-SR scale was considered “very low” and the level of recommendation was C.

3.3. The Motivation and Pleasure Scale Self-Report (MAPS-SR)

The Motivation and Pleasure Self-Report scale (MAP-SR) [16] is derived from the CAINS-SR and comprises 3 negative dimensions: anhedonia, avolition, and social withdrawal. This 15-item scale assesses consummatory and anticipatory pleasure related to social, recreational, and work domains, as well as motivation related to family and activities.

3.3.1. Risk of Bias and Criteria for Good Measurement Properties

Structural validity was assessed in two [28,29] of the seven validation studies of the MAP-SR [16,28,29,30,31,32,33]. One study [28] received a “very good” rating for risk of bias and a “positive” rating for measurement properties, indicating an adequate fit for a four-factor model. In contrast, the other study [29] received a “doubtful” rating for risk of bias due to a sample size of less than 100 and a “negative” rating for measurement properties, as some factor loadings did not reach the 0.30 threshold.
All seven validation studies of the MAP-SR assessed internal consistency [16,28,29,30,31,32,33]; however, only two studies [28,29] evaluated structural validity, receiving a “very good” rating for risk of bias and a “positive” rating for measurement properties. The remaining studies [16,30,31,32,33] did not include factor analysis, resulting in “doubtful” ratings and “indeterminate” outcomes due to insufficient evidence supporting adequate structural validity for the MAP-SR.
Only two studies assessed the reliability of the MAP-SR [28,29], both receiving an “adequate” rating for risk of bias. One study [28] achieved a “positive” rating for measurement properties, while the other [29] received a “negative” rating due to its failure to meet the 0.7 threshold for correlation coefficients across all subscales.
All seven MAP-SR validation studies [16,28,29,30,31,32,33] conducted hypothesis testing for both convergent and discriminant validity. Five studies received an “adequate'” rating [16,28,30,31,32] for risk of bias, while two were rated 'very good' [29,33]. Overall, the studies achieved a “positive” rating for the measurement properties of convergent validity [16,28,30,31,32,33], except for one study [29], which received a “negative” rating due to correlation coefficients below 0.5. Convergent validity was established by comparing the MAP-SR with various scales, including the BPRS negative subscore [27], the Positive and Negative Syndrome Scale (PANSS) negative subscore [34], the Scale for the Assessment of Negative Symptoms (SANS) [35], CAINS [14], SNS [15], and the Temporal Experience of Pleasure Scale (TEPS) [36]. For discriminant validity, four studies [16,28,30,33] were rated as “positive” for comparing the MAP-SR against scales for depression, positive symptoms, quality of life, and medication side effects. However, three studies [29,31,32] received an “indeterminate” rating. Two of these studies assessed discriminant validity solely through correlations with depression scales, which yielded moderate correlations that were insufficient to confirm strong discriminant validity [31,32]. Additionally, the authors of one study did not clearly state specific hypotheses regarding discriminant validity [29].

3.3.2. GRADE Evaluation

There were either multiple studies of adequate quality or a single study of very good quality available for structural validity, reliability, internal consistency, and hypothesis testing for both construct convergent and discriminant validity. Consequently, no downgrading was applied.
Due to the inconsistency in the results of the reliability studies, a -1 downgrade was applied.
For imprecision, with the overall sample size for the MAPS-SR being n = 676, no downgrade was applied.
Thus, the overall quality of the evidence for the MAPS-SR scale was considered “moderate” and the level of recommendation was A.

3.4. The Self Evaluation of Negative Symptoms (SNS)

The Self-evaluation of Negative Symptoms (SNS) [15] provides an assessment of all five domains of NS using 20 items, scored from 0 (no symptoms) to 40 (severe negative symptoms), within a brief timeframe. The SNS is available in 27 languages (see https://sns-dollfus.com), ensuring global accessibility.

3.4.1. Risk of Bias and Criteria for Good Measurement Properties

Among the seventeen validation studies of the SNS [9,15,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51], nine [15,37,38,39,40,41,42,48,49] specifically assessed its structural validity. Of these, five studies [15,38,39,40,42] were rated as “inadequate” in terms of risk of bias, primarily due to an insufficient number of participants for factor analysis (fewer than five times the number of items on the scale). One study [37] received a “doubtful” rating due to the inappropriate use of principal component analysis. In contrast, three studies [41,48,49] received a “very good” rating for structural validity. Regarding measurement properties, eight studies were rated as “positive” [15,37,38,39,40,41,48,49], demonstrating a good fit for either a two-factor model [15,38,40] or a five-factor model [37,39,41,48,49], while only one study [42] was rated as “indeterminate”.
Twelve studies [15,37,38,39,40,41,42,43,44,45,46,47] assessed the internal consistency of the SNS. Among these, one study [41] was rated as having a “very good” risk of bias, while eleven studies [15,37,38,39,40,42,43,44,45,46,47] were deemed “doubtful.” The primary reasons for this rating included the absence of Cronbach's alpha calculations for all subscales and insufficient information regarding the scale's structure, either due to a lack of factor analysis or the use of an inadequate model. In terms of measurement properties, four studies [15,38,40,42] received “positive” ratings, whereas two studies [39,41] were rated “negatively” because their Cronbach's alpha coefficients fell below the accepted threshold of 0.7. Additionally, six studies [43,45,46,47,52,53] received “indeterminate” ratings, as they failed to meet the criteria for providing at least minimal evidence of sufficient structural validity or lacked Cronbach's alpha calculations for all SNS subscales.
The reliability of the SNS was assessed in four studies [15,37,42,43]. Two studies [15,42] received “very good” ratings for risk of bias and “positive” ratings for measurement properties, as they reported ICC values exceeding 0.7. In contrast, one study [52] was rated as having an “adequate” risk of bias but received a “negative” rating for measurement properties, with all ICC scores falling below the 0.7 threshold. Finally, another study [43] was rated as “inadequate” for risk of bias due to its reliance on a t-test for reliability assessment, rather than the recommended methods. Consequently, this study also received an “indeterminate” rating for its measurement properties.
Five studies with a “very good” risk of bias rating evaluated criterion validity [9,40,41,50,51]. All of these studies received a “positive” rating for measurement properties, with area under the curve (AUC) values greater than 0.7. The results demonstrate that the SNS is able to identify thresholds for the severity of NS among patients at ultra-high risk of psychosis [51], experiencing their first episode of psychosis [50], diagnosed with schizophrenia [9,41], or presenting with a deficit subtype [40].
Finally, hypothesis testing for construct convergent validity was conducted across thirteen validation studies for the SNS [15,37,38,39,40,41,42,43,44,45,46,47,48]. The risk of bias was rated as “very good” for eight studies [15,41,42,45,46,47,48,52] and “adequate” for five studies [38,39,40,43,44]. Regarding measurement properties, twelve studies received a “positive” rating [15,37,38,39,40,41,43,44,45,46,47,48]. Only one study [42] received a “negative” rating because the correlations failed to reach the threshold of 0.5 with other measures of NS. In the various studies, the SNS was compared with the Scale for the Assessment of Negative Symptoms (SANS) [35], the BPRS negative subscore [27], the PANSS negative subscore [34], the Clinical Global Impression (CGI) negative subscore [54], the BNSS [55], the Negative Symptom Assessment 16 (NSA-16) [56] and the CAINS [14] for convergent validity. In evaluating hypothesis testing for construct discriminant validity, nine studies [15,38,39,42,43,45,47,48,52] were included. Among them, three studies [15,42,48] received a “very good” rating for risk of bias, while four studies [38,39,43,52] were rated as “adequate”. All of them [15,38,39,42,43,48,52] obtained a “positive” rating for measurement properties. These studies effectively compared the SNS with scales assessing depression, parkinsonism, and positive symptoms to determine discriminant validity. Conversely, two studies [45,47] were rated as 'doubtful' for risk of bias and received an 'indeterminate' rating for measurement properties due to their exclusive use of a quality of life scale, which is insufficient for determining discriminant validity.

3.4.2. GRADE Evaluation

Since there were several studies of at least adequate quality, or one study of very good quality available for each criterion, the scale was not downgraded in terms of its risk of bias.
Concerning inconsistency, only internal consistency and reliability showed conflicting results, which led to a downgrade of -1. Inconsistency was not considered in hypothesis testing for construct convergent validity, as eleven studies reported “positive” outcomes and only one received a “negative” rating.
For imprecision, with the overall sample size for the SNS being n = 1835, no downgrade was applied.
Thus, the overall quality of the evidence for the SNS scale was considered “moderate”, and the level of recommendation was A.

3.5. The Negative Symptoms Inventory Self-Report (NSI-SR)

The Negative Symptoms Inventory Self-Report (NSI-SR) [24] evaluates three domains of negative symptomatology (avolition, anhedonia, and social withdrawal) with 11 items. This study was conducted with students, individuals at ultra-high risk of psychosis, and those with schizophrenia.

3.5.1. Risk of Bias and Criteria for Good Measurement Properties

Only one study [24] evaluated the psychometric properties of the NSI-SR, focusing on structural validity, internal consistency, reliability, and hypothesis testing for construct convergent and discriminant validity.
The risk of bias was assessed as “very good” for structural validity, supported by a confirmatory factor analysis conducted with an adequate number of subjects. Measurement properties were rated as “positive”, supported by favorable fit indices from the confirmatory factor analysis, which identified a three-factor model.
The internal consistency of the NSI-SR was rated as “very good” for risk of bias and received a “positive” rating for measurement properties, with Cronbach’s alpha exceeding 0.7 for all three factors of the scale.
The risk of bias for reliability was rated as “adequate,” and the measurement properties were rated as “negative” due to correlation scores below 0.7.
Finally, the risk of bias for hypothesis testing of construct convergent and discriminant validity was rated as “very good.” Regarding measurement properties, convergent validity, assessed using BNSS scores [13], received a “negative” rating due to low correlation levels. In contrast, discriminant validity was also rated as “negative” because of positive correlations with scores from depression and hallucination scales.

3.5.2. GRADE Evaluation

Since there was only one study [24] of adequate quality assessing reliability, this resulted in a “serious” risk of bias and a downgrade of -1.
The criterion for inconsistency was not applicable, as there was only one validation study available with determinable results.
For imprecision, since the sample size was 62, an additional downgrade of -1 was applied.
Thus, the overall quality of the evidence for the NSI-SR scale was considered “low”, and the level of recommendation was B.

4. Discussion

This review highlights various self-assessment instruments specifically designed for the evaluation of several dimensions of NS in patients with schizophrenia, schizoaffective disorder, a first episode of psychosis, or those at ultra-high risk of psychosis. We have rigorously evaluated their psychometric properties to facilitate their application in clinical practice and research. In the following discussion, we will delve into the strengths, weaknesses, and recommendations for the different tools.
Among the scales that cover several dimensions of NS, three (SENS [25], CAINS-SR [26], and SNS [15]) assess five domains of NS, while two others assess three domains. Although the SENS [25] provides comprehensive coverage, it has significant limitations. One limitation concerns the assessment of anhedonia, as it fails to account for its two dimensions: anticipatory and consummatory pleasure. Additionally, the inclusion of 'attention' has been a subject of debate, as it may be more closely related to cognitive deficits rather than NS [5]. The COSMIN evaluation further highlights weaknesses, with only one validation study available [25]. This study reported negative ratings for test-retest reliability, indeterminate results for internal consistency, and the absence of structural validity testing or adequate hypothesis testing for construct validity (both convergent and discriminant). As a result, the scale has a recommendation rating of C.
Similarly, the CAINS-SR [26] offers a comprehensive evaluation of all domains of negative symptomatology. However, its psychometric properties have been examined in only one study [26]. While this study reported promising results in hypothesis testing of construct convergent and discriminant validity, there is insufficient information regarding other validation domains. Given the limited evidence available, it has received a recommendation rating of C.
In contrast, the SNS [15] demonstrates robust psychometric properties and effectively assesses all five domains of negative symptomatology, including both anticipatory and consummatory anhedonia. A notable strength of this scale is its ability to identify thresholds in the severity of NS among patients with schizophrenia [9], first-episode psychosis [50], healthy adolescents [57], and students [51]. This highlights the SNS's capability to detect NS across diverse populations. Numerous studies [8,9,10,11,12,13,14,15,16,17,18,19,20,21], including several of high quality [41,48,49], have evaluated the psychometric properties of the SNS, demonstrating strong results across all measurement domains. These findings support a grade A recommendation for using the SNS in both clinical and research settings for the schizophrenia population.
Other tools, such as the MAP-SR [16] and NSI-SR [24] offer targeted assessments of key NS domains, including asociality, avolition, and anhedonia. The MAP-SR [16] provides a detailed evaluation of anticipatory and consummatory anhedonia across various contexts (social, recreational, and professional) and assesses motivation in family relationships and activities [16]. This specificity enhances the understanding of these critical dimensions of NS, which are often challenging to evaluate accurately. Several high-quality studies [16,28,30,31,32] have evaluated the MAP-SR, confirming its strong psychometric properties and supporting a grade A recommendation for its use in routine practice and research in the schizophrenia population.
Lastly, the NSI-SR [24] assesses both consummatory and anticipatory pleasure, facilitating a focused evaluation of anhedonia. It also measures social withdrawal and engagement in social activities, effectively highlighting challenges in social interactions. Additionally, it addresses avolition through items related to motivation and the initiation of activities. A notable strength of the NSI-SR is its validation across diverse populations, including students, individuals at ultra-high risk of psychosis, and those with schizophrenia, enhancing its capacity to detect NS in various contexts [24]. However, the psychometric properties of the NSI-SR have been evaluated in only one study [24]. While this research reported promising findings regarding structural validity and internal consistency, other evaluations highlighted poor performance in test-retest reliability and hypothesis testing for construct convergent and discriminant validity. Due to the limited number of validation studies, the NSI-SR has been assigned a recommendation rating of B.
To summarize, among the tools designed to assess the five domains of negative symptomatology, the SNS [15] stands out with a distinguished grade A recommendation, reflecting its robust psychometric properties. Additionally , the MAP-SR [16] also earns a grade A recommendation, positioning it as an excellent option for focused evaluations of anhedonia, avolition, and social withdrawal, thereby enriching our clinical understanding of these critical dimensions.
In addition to these self-assessment tools, other instruments focus on single dimensions of NS, limiting their clinical utility in offering a comprehensive view of the patient's condition. For example, the Temporal Experience of Pleasure Scale (TEPS) [58] specifically targets anhedonia, while the BIRT Motivation Questionnaire (BMQ-S) [59] measures motivational deficits. These focused tools are valuable in research and specific clinical contexts, such as cognitive behavioral therapy, which has been shown to be effective in addressing symptoms related to the avolition-apathy dimension of NS [18]. Assessing these particular aspects of NS can be highly relevant, as it allows clinicians to guide targeted interventions—such as behavioral activation strategies for avolition or activities designed to foster enjoyment [18]. However, their narrow focus limits their ability to provide a comprehensive understanding of the multiple dimensions of NS [19], potentially overlooking the synergistic effects between NS domains and their cumulative impact on patient functioning [60]. Therefore, without the integration of multi-dimensional scales, single-dimension tools may fail to capture the full complexity of NS, potentially leading to incomplete assessments, missed treatment effects, and suboptimal care planning [61]. In contrast, multi-dimensional tools offer a more holistic assessment by examining the interplay between different domains of NS and their combined effect on daily functioning [62]. This is crucial for identifying distinct NS profiles, which can help inform personalized therapeutic strategies. Moreover, in clinical trials assessing the effects of antipsychotics on secondary NS and experimental treatments targeting NS, such as neurostimulation interventions, multi-dimensional tools are indispensable for capturing subtle, multi-faceted changes across various dimensions of NS [1]. These tools also play a pivotal role in research, as they enable a broader dataset to correlate clinical symptoms with neurobiological markers, enhancing our understanding of NS mechanisms and informing the development of future treatments.
In spite of the European Association's recommendation [17], the use of self-assessment scales remains limited, even though robust tools are available. While Weigel et al. [7] assessed the psychometric properties of hetero-evaluation tools for NS, including the SANS [35], High Royds Evaluation of Negativity Scale (HEN) [63], and Negative Symptom Assessment-16 (NSA-16) [56], concluding that these tools are unsuitable for clinical practice, other studies have highlighted the strong psychometric properties of newer instruments such as the BNSS and the CAINS [6,8]. Specifically, Wehr et al. [6] highlighted the robust measurement properties of the CAINS in terms of structural validity, internal consistency, and reliability, while Weigel et al. [8] underscored the strong structural validity, internal consistency, and interrater reliability of the BNSS across various contexts. In In the same vein, our study focuses on self-assessment tools and underscores the strong psychometric properties of the SNS [15] and the MAP-SR [16], which provide alternatives for clinical and research applications. These self-assessment scales, with their robust validation, could complement traditional observer-rated evaluations, contributing to a more comprehensive approach to NS assessment, as recommended by the European Psychiatric Association [17]. The incorporation of self-assessment scales into clinical routines is crucial, as they can significantly enhance our understanding of patients' experiences [9,10] and inform the development of personalized treatment strategies. Furthermore, incorporating self-assessments into emerging technologies, such as digital platforms and ecological momentary assessments, could facilitate real-time data collection, enabling the capture of fluctuations in NS and their interactions with motivational factors in patients' daily lives [64]. By leveraging digital platforms, clinicians can gain deeper insights into patients' experiences, thereby enhancing the accuracy of self-reports and fostering more personalized approaches to care [64,65].
Despite employing a recommended methodology (COSMIN), our study has several potential limitations. First, data extraction and analysis were conducted by a single reviewer, which may introduce bias or lead to oversight in the interpretation of results. To mitigate this concern, we used the COSMIN framework, a robust tool for evaluating the psychometric properties of assessment instruments. Second, we did not perform a meta-analysis to confirm our findings due to the diverse nature of the data, which prevented us from quantitatively summarizing the results. Such an analysis would have provided a more precise estimate of the psychometric properties across studies, potentially revealing overall effect sizes and the variability in results. Finally, no protocol was established prior to conducting this review, and the process was not registered. However, the review was carried out following standard systematic approaches, with clear inclusion and exclusion criteria, ensuring transparency and minimizing bias. The absence of a formal registration does not affect the reliability or validity of the findings, as the methodology remained consistent with established practices in the field.

5. Conclusions

In conclusion, this review emphasizes that, despite the underuse of self-assessment scales for NS in schizophrenia, several scales are available for clinicians and researchers. Among these, two instruments receive a Grade A recommendation for clinical or research practice: the SNS [15] for assessing the five domains of NS and the MAPS-SR [16] for evaluating three negative dimensions: anhedonia, avolition, and social withdrawal.

6. Future Directions

Future research should prioritize enhancing the psychometric properties of existing self-assessment scales for measuring NS in schizophrenia. This should include longitudinal studies to establish test-retest reliability and investigate how demographic and clinical factors affect scale performance. Furthermore, validating these tools in diverse clinical settings, including both outpatient programs and inpatient units, is crucial. Ultimately, this will help integrate these scales into routine clinical practice and improve outcomes for individuals with schizophrenia.

Author Contributions

L.M analyzed the literature and wrote the first draft of the paper. SD revised the paper. Both reviewed and approved the final version.

Funding

“L.M obtained a phD grand from the RHU PSYCARE (ANR-18-RHU-0014).

Informed Consent Statement

Not applicable.

Data Availability Statement

No new data was created or analyzed in this study. Data sharing is not applicable to this article.

Conflicts of Interest

The authors declare no conflicts of interest.

Appendix A

Table A1. PRISMA checklist.
Table A1. PRISMA checklist.
Section and Topic Item # Checklist item Location where item is reported
TITLE
Title 1 Identify the report as a systematic review. Yes
ABSTRACT
Abstract 2 See the PRISMA 2020 for Abstracts checklist. Yes
INTRODUCTION
Rationale 3 Describe the rationale for the review in the context of existing knowledge. Yes
Objectives 4 Provide an explicit statement of the objective(s) or question(s) the review addresses. Yes
METHODS
Eligibility criteria 5 Specify the inclusion and exclusion criteria for the review and how studies were grouped for the syntheses. Yes
Information sources 6 Specify all databases, registers, websites, organisations, reference lists and other sources searched or consulted to identify studies. Specify the date when each source was last searched or consulted. Yes
Search strategy 7 Present the full search strategies for all databases, registers and websites, including any filters and limits used. Yes
Selection process 8 Specify the methods used to decide whether a study met the inclusion criteria of the review, including how many reviewers screened each record and each report retrieved, whether they worked independently, and if applicable, details of automation tools used in the process. Yes
Data collection process 9 Specify the methods used to collect data from reports, including how many reviewers collected data from each report, whether they worked independently, any processes for obtaining or confirming data from study investigators, and if applicable, details of automation tools used in the process. Yes
Data items 10a List and define all outcomes for which data were sought. Specify whether all results that were compatible with each outcome domain in each study were sought (e.g. for all measures, time points, analyses), and if not, the methods used to decide which results to collect. Yes
10b List and define all other variables for which data were sought (e.g. participant and intervention characteristics, funding sources). Describe any assumptions made about any missing or unclear information. Yes
Study risk of bias assessment 11 Specify the methods used to assess risk of bias in the included studies, including details of the tool(s) used, how many reviewers assessed each study and whether they worked independently, and if applicable, details of automation tools used in the process. Yes
Effect measures 12 Specify for each outcome the effect measure(s) (e.g. risk ratio, mean difference) used in the synthesis or presentation of results. NA
Synthesis methods 13a Describe the processes used to decide which studies were eligible for each synthesis (e.g. tabulating the study intervention characteristics and comparing against the planned groups for each synthesis (item #5)). Yes
13b Describe any methods required to prepare the data for presentation or synthesis, such as handling of missing summary statistics, or data conversions. NA
13c Describe any methods used to tabulate or visually display results of individual studies and syntheses. Yes
13d Describe any methods used to synthesize results and provide a rationale for the choice(s). If meta-analysis was performed, describe the model(s), method(s) to identify the presence and extent of statistical heterogeneity, and software package(s) used. Yes
13e Describe any methods used to explore possible causes of heterogeneity among study results (e.g. subgroup analysis, meta-regression). NA
13f Describe any sensitivity analyses conducted to assess robustness of the synthesized results. NA
Reporting bias assessment 14 Describe any methods used to assess risk of bias due to missing results in a synthesis (arising from reporting biases). NA
Certainty assessment 15 Describe any methods used to assess certainty (or confidence) in the body of evidence for an outcome. Yes
RESULTS
Study selection 16a Describe the results of the search and selection process, from the number of records identified in the search to the number of studies included in the review, ideally using a flow diagram. Yes
16b Cite studies that might appear to meet the inclusion criteria, but which were excluded, and explain why they were excluded. NA
Study characteristics 17 Cite each included study and present its characteristics. Yes
Risk of bias in studies 18 Present assessments of risk of bias for each included study. Yes
Results of individual studies 19 For all outcomes, present, for each study: (a) summary statistics for each group (where appropriate) and (b) an effect estimate and its precision (e.g. confidence/credible interval), ideally using structured tables or plots. NA
Results of syntheses 20a For each synthesis, briefly summarise the characteristics and risk of bias among contributing studies. Yes
20b Present results of all statistical syntheses conducted. If meta-analysis was done, present for each the summary estimate and its precision (e.g. confidence/credible interval) and measures of statistical heterogeneity. If comparing groups, describe the direction of the effect. Yes
20c Present results of all investigations of possible causes of heterogeneity among study results. Yes
20d Present results of all sensitivity analyses conducted to assess the robustness of the synthesized results. NA
Reporting biases 21 Present assessments of risk of bias due to missing results (arising from reporting biases) for each synthesis assessed. NA
Certainty of evidence 22 Present assessments of certainty (or confidence) in the body of evidence for each outcome assessed. Yes
DISCUSSION
Discussion 23a Provide a general interpretation of the results in the context of other evidence. Yes
23b Discuss any limitations of the evidence included in the review. Yes
23c Discuss any limitations of the review processes used. Yes
23d Discuss implications of the results for practice, policy, and future research. Yes
OTHER INFORMATION
Registration and protocol 24a Provide registration information for the review, including register name and registration number, or state that the review was not registered. Yes
24b Indicate where the review protocol can be accessed, or state that a protocol was not prepared. Yes
24c Describe and explain any amendments to information provided at registration or in the protocol. Yes
Support 25 Describe sources of financial or non-financial support for the review, and the role of the funders or sponsors in the review. Yes
Competing interests 26 Declare any competing interests of review authors. Yes
Availability of data, code and other materials 27 Report which of the following are publicly available and where they can be found: template data collection forms; data extracted from included studies; data used for all analyses; analytic code; any other materials used in the review. Yes
From: Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 2021;372:n71. doi: 10.1136/bmj.n71. This work is licensed under CC BY 4.0. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.

References

  1. Kirkpatrick, B.; Fenton, W.S.; Carpenter, W.T.; Marder, S.R. The NIMH-MATRICS Consensus Statement on Negative Symptoms. Schizophr Bull 2006, 32, 214–219. https://doi.org/10.1093/schbul/sbj053. [CrossRef]
  2. Sicras-Mainar, A.; Maurino, J.; Ruiz-Beato, E.; Navarro-Artieda, R. Impact of Negative Symptoms on Healthcare Resource Utilization and Associated Costs in Adult Outpatients with Schizophrenia: A Population-Based Study. BMC Psychiatry 2014, 14, 225. https://doi.org/10.1186/s12888-014-0225-8. [CrossRef]
  3. Montvidas, J.; Adomaitienė, V.; Leskauskas, D.; Dollfus, S. Health-Related Quality of Life Prediction Using the Self-Evaluation of Negative Symptoms Scale (SNS) in Patients with Schizophrenia. Nordic Journal of Psychiatry 2021, 75, S21–S21. https://doi.org/10.1080/08039488.2021.2019934. [CrossRef]
  4. Stahl, S.M.; Buckley, P.F. Negative Symptoms of Schizophrenia: A Problem That Will Not Go Away. Acta Psychiatr Scand 2007, 115, 4–11. https://doi.org/10.1111/j.1600-0447.2006.00947.x. [CrossRef]
  5. Lincoln, T.M.; Dollfus, S.; Lyne, J. Current Developments and Challenges in the Assessment of Negative Symptoms. Schizophr Res 2017, 186, 8–18. https://doi.org/10.1016/j.schres.2016.02.035. [CrossRef]
  6. Wehr, S.; Weigel, L.; Davis, J.; Galderisi, S.; Mucci, A.; Leucht, S. Clinical Assessment Interview for Negative Symptoms (CAINS): A Systematic Review of Measurement Properties. Schizophr Bull 2024, 50, 747–756. https://doi.org/10.1093/schbul/sbad137. [CrossRef]
  7. Weigel, L.; Wehr, S.; Galderisi, S.; Mucci, A.; Davis, J.M.; Leucht, S. Clinician-Reported Negative Symptom Scales: A Systematic Review of Measurement Properties. Schizophr Bull 2024, sbae168. https://doi.org/10.1093/schbul/sbae168. [CrossRef]
  8. Weigel, L.; Wehr, S.; Galderisi, S.; Mucci, A.; Davis, J.; Giordano, G.M.; Leucht, S. The Brief Negative Symptom Scale (BNSS): A Systematic Review of Measurement Properties. Schizophrenia (Heidelb) 2023, 9, 45. https://doi.org/10.1038/s41537-023-00380-x. [CrossRef]
  9. Dollfus, S.; Delouche, C.; Hervochon, C.; Mach, C.; Bourgeois, V.; Rotharmel, M.; Tréhout, M.; Vandevelde, A.; Guillin, O.; Morello, R. Specificity and Sensitivity of the Self-Assessment of Negative Symptoms (SNS) in Patients with Schizophrenia. Schizophrenia Research 2019, 211, 51–55. https://doi.org/10.1016/j.schres.2019.07.012. [CrossRef]
  10. Lindström, E.; Lewander, T.; Malm, U.; Malt, U.F.; Lublin, H.; Ahlfors, U.G. Patient-Rated versus Clinician-Rated Side Effects of Drug Treatment in Schizophrenia. Clinical Validation of a Self-Rating Version of the UKU Side Effect Rating Scale (UKU-SERS-Pat). Nord J Psychiatry 2001, 55 Suppl 44, 5–69. https://doi.org/10.1080/080394801317084428. [CrossRef]
  11. Eisen, S.V.; Dickey, B.; Sederer, L.I. A Self-Report Symptom and Problem Rating Scale to Increase Inpatients’ Involvement in Treatment. Psychiatr Serv 2000, 51, 349–353. https://doi.org/10.1176/appi.ps.51.3.349. [CrossRef]
  12. Niv, N.; Cohen, A.N.; Mintz, J.; Ventura, J.; Young, A.S. The Validity of Using Patient Self-Report to Assess Psychotic Symptoms in Schizophrenia. Schizophr Res 2007, 90, 245–250. https://doi.org/10.1016/j.schres.2006.11.011. [CrossRef]
  13. Kirkpatrick, B.; Strauss, G.P.; Nguyen, L.; Fischer, B.A.; Daniel, D.G.; Cienfuegos, A.; Marder, S.R. The Brief Negative Symptom Scale: Psychometric Properties. Schizophr Bull 2011, 37, 300–305. https://doi.org/10.1093/schbul/sbq059. [CrossRef]
  14. Kring, A.M.; Gur, R.E.; Blanchard, J.J.; Horan, W.P.; Reise, S.P. The Clinical Assessment Interview for Negative Symptoms (CAINS): Final Development and Validation. Am J Psychiatry 2013, 170, 165–172. https://doi.org/10.1176/appi.ajp.2012.12010109. [CrossRef]
  15. Dollfus, S.; Mach, C.; Morello, R. Self-Evaluation of Negative Symptoms: A Novel Tool to Assess Negative Symptoms. Schizophr Bull 2016, 42, 571–578. https://doi.org/10.1093/schbul/sbv161. [CrossRef]
  16. Llerena, K.; Park, S.G.; McCarthy, J.M.; Couture, S.M.; Bennett, M.E.; Blanchard, J.J. The Motivation and Pleasure Scale-Self-Report (MAP-SR): Reliability and Validity of a Self-Report Measure of Negative Symptoms. Compr Psychiatry 2013, 54, 568–574. https://doi.org/10.1016/j.comppsych.2012.12.001. [CrossRef]
  17. Galderisi, S.; Mucci, A.; Dollfus, S.; Nordentoft, M.; Falkai, P.; Kaiser, S.; Giordano, G.M.; Vandevelde, A.; Nielsen, M.Ø.; Glenthøj, L.B.; et al. EPA Guidance on Assessment of Negative Symptoms in Schizophrenia. Eur Psychiatry 2021, 64, e23. https://doi.org/10.1192/j.eurpsy.2021.11. [CrossRef]
  18. Schormann, A.L.A.; Pillny, M.; Haß, K.; Lincoln, T.M. “Goals in Focus”-a Targeted CBT Approach for Motivational Negative Symptoms of Psychosis: Study Protocol for a Randomized-Controlled Feasibility Trial. Pilot Feasibility Stud 2023, 9, 72. https://doi.org/10.1186/s40814-023-01284-4. [CrossRef]
  19. Grant, P.M.; Huh, G.A.; Perivoliotis, D.; Stolar, N.M.; Beck, A.T. Randomized Trial to Evaluate the Efficacy of Cognitive Therapy for Low-Functioning Patients with Schizophrenia. Arch Gen Psychiatry 2012, 69, 121–127. https://doi.org/10.1001/archgenpsychiatry.2011.129. [CrossRef]
  20. Moher, D.; Liberati, A.; Tetzlaff, J.; Altman, D.G. Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement. Journal of Clinical Epidemiology 2009, 62, 1006–1012. https://doi.org/10.1016/j.jclinepi.2009.06.005. [CrossRef]
  21. Prinsen, C. a. C.; Mokkink, L.B.; Bouter, L.M.; Alonso, J.; Patrick, D.L.; de Vet, H.C.W.; Terwee, C.B. COSMIN Guideline for Systematic Reviews of Patient-Reported Outcome Measures. Qual Life Res 2018, 27, 1147–1157. https://doi.org/10.1007/s11136-018-1798-3. [CrossRef]
  22. Mokkink, L.B.; de Vet, H.C.W.; Prinsen, C. a. C.; Patrick, D.L.; Alonso, J.; Bouter, L.M.; Terwee, C.B. COSMIN Risk of Bias Checklist for Systematic Reviews of Patient-Reported Outcome Measures. Qual Life Res 2018, 27, 1171–1179. https://doi.org/10.1007/s11136-017-1765-4. [CrossRef]
  23. Terwee, C.B.; Mokkink, L.B.; Knol, D.L.; Ostelo, R.W.J.G.; Bouter, L.M.; de Vet, H.C.W. Rating the Methodological Quality in Systematic Reviews of Studies on Measurement Properties: A Scoring System for the COSMIN Checklist. Qual Life Res 2012, 21, 651–657. https://doi.org/10.1007/s11136-011-9960-1. [CrossRef]
  24. Raugh, I.M.; Luther, L.; Bartolomeo, L.A.; Gupta, T.; Ristanovic, I.; Pelletier-Baldelli, A.; Mittal, V.A.; Walker, E.F.; Strauss, G.P. Negative Symptom Inventory-Self-Report (NSI-SR): Initial Development and Validation. Schizophrenia Research 2023, 256, 79–87. https://doi.org/10.1016/j.schres.2023.04.015. [CrossRef]
  25. Selten, J.P.; Sijben, N.E.; van den Bosch, R.J.; Omloo-Visser, J.; Warmerdam, H. The Subjective Experience of Negative Symptoms: A Self-Rating Scale. Compr Psychiatry 1993, 34, 192–197. https://doi.org/10.1016/0010-440x(93)90047-8. [CrossRef]
  26. Park, S.G.; Llerena, K.; McCarthy, J.M.; Couture, S.M.; Bennett, M.E.; Blanchard, J.J. Screening for Negative Symptoms: Preliminary Results from the Self-Report Version of the Clinical Assessment Interview for Negative Symptoms. Schizophr Res 2012, 135, 139–143. https://doi.org/10.1016/j.schres.2011.12.007. [CrossRef]
  27. Overall, J.E.; Gorham, D.R. The Brief Psychiatric Rating Scale. Psychol Rep 1962, 10, 799–812. https://doi.org/10.2466/pr0.1962.10.3.799. [CrossRef]
  28. Wang, L.-L.; Ma, E.P.Y.; Lui, S.S.Y.; Cheung, E.F.C.; Cheng, K.S.; Chan, R.C.K. Validation and Extension of the Motivation and Pleasure Scale-Self Report (MAP-SR) across the Schizophrenia Spectrum in the Chinese Context. Asian J Psychiatr 2020, 49, 101971. https://doi.org/10.1016/j.ajp.2020.101971. [CrossRef]
  29. Richter, J.; Hesse, K.; Eberle, M.-C.; Eckstein, K.N.; Zimmermann, L.; Schreiber, L.; Burmeister, C.P.; Wildgruber, D.; Klingberg, S. Self-Assessment of Negative Symptoms – Critical Appraisal of the Motivation and Pleasure – Self-Report’s (MAP-SR) Validity and Reliability. Comprehensive Psychiatry 2019, 88, 22–28. https://doi.org/10.1016/j.comppsych.2018.10.007. [CrossRef]
  30. Engel, M.; Lincoln, T.M. Motivation and Pleasure Scale-Self-Report (MAP-SR): Validation of the German Version of a Self-Report Measure for Screening Negative Symptoms in Schizophrenia. Compr Psychiatry 2016, 65, 110–115. https://doi.org/10.1016/j.comppsych.2015.11.001. [CrossRef]
  31. García-Portilla, M.P.; García-Álvarez, L.; de la Fuente-Tomás, L.; Dal Santo, F.; Velasco, A.; González-Blanco, L.; Zurrón-Madera, P.; Fonseca-Pedrero, E.; Bobes-Bascarán, M.T.; Sáiz, P.A.; et al. Spanish Validation of the MAP-SR: Two Heads Better Than One for the Assessment of Negative Symptoms of Schizophrenia. Psicothema 2021, 33, 473–480. https://doi.org/10.7334/psicothema2020.457. [CrossRef]
  32. Cernvall, M.; Bengtsson, J.; Bodén, R. The Swedish Version of the Motivation and Pleasure Scale Self-Report (MAP-SR): Psychometric Properties in Patients with Schizophrenia or Depression. Nord J Psychiatry 2024, 78, 339–346. https://doi.org/10.1080/08039488.2024.2324060. [CrossRef]
  33. Kim, J.-S.; Jang, S.-K.; Park, S.-C.; Yi, J.-S.; Park, J.-K.; Lee, J.S.; Choi, K.-H.; Lee, S.-H. Measuring Negative Symptoms in Patients with Schizophrenia: Reliability and Validity of the Korean Version of the Motivation and Pleasure Scale-Self-Report. Neuropsychiatr Dis Treat 2016, 12, 1167–1172. https://doi.org/10.2147/NDT.S107775. [CrossRef]
  34. Kay, S.R.; Fiszbein, A.; Opler, L.A. The Positive and Negative Syndrome Scale (PANSS) for Schizophrenia. Schizophr Bull 1987, 13, 261–276. https://doi.org/10.1093/schbul/13.2.261. [CrossRef]
  35. Andreasen, N.C. The Scale for the Assessment of Negative Symptoms (SANS): Conceptual and Theoretical Foundations. Br J Psychiatry Suppl 1989, 49–58.
  36. Loas, G.; Monestes, J.-L.; Ameller, A.; Bubrovszky, M.; Yon, V.; Wallier, J.; Berthoz, S.; Corcos, M.; Thomas, P.; Gard, D.E. Traduction et Étude de Validation de La Version Française de l’échelle d’expérience Temporelle Du Plaisir (EETP, Temporal Experience of Pleasure Scale [TEPS], Gard et al., 2006) : Étude Chez 125 Étudiants et Chez 162 Sujets Présentant Un Trouble Psychiatrique. Annales Médico-psychologiques, revue psychiatrique 2009, 167, 641–648. https://doi.org/10.1016/j.amp.2009.09.002. [CrossRef]
  37. Hajj, A.; Hallit, S.; Chamoun, K.; Sacre, H.; Obeid, S.; Haddad, C.; Dollfus, S.; Rabbaa Khabbaz, L. Validation of the Arabic Version of the “Self-Evaluation of Negative Symptoms” Scale (SNS). BMC Psychiatry 2020, 20, 240. https://doi.org/10.1186/s12888-020-02647-4. [CrossRef]
  38. Montvidas, J.; Adomaitienė, V.; Leskauskas, D.; Dollfus, S. Validation of the Lithuanian Version of the Self-Evaluation of Negative Symptoms Scale (SNS). Nordic Journal of Psychiatry 2021, 75, 351–355. https://doi.org/10.1080/08039488.2020.1862295. [CrossRef]
  39. Polat, I.; Ince Guliyev, E.; Elmas, S.; Karakaş, S.; Aydemir, Ö.; Üçok, A. Validation of the Turkish Version of the Self-Evaluation of Negative Symptoms Scale (SNS). Int J Psychiatry Clin Pract 2022, 26, 221–227. https://doi.org/10.1080/13651501.2022.2082985. [CrossRef]
  40. Samochowiec, J.; Jabłoński, M.; Plichta, P.; Piotrowski, P.; Stańczykiewicz, B.; Bielawski, T.; Misiak, B. The Self-Evaluation of Negative Symptoms in Differentiating Deficit Schizophrenia: The Comparison of Sensitivity and Specificity with Other Tools. Psychopathology 2023, 56, 453–461. https://doi.org/10.1159/000529244. [CrossRef]
  41. Chen, G.; Chen, J.; Tian, H.; Lin, C.; Zhu, J.; Ping, J.; Chen, L.; Zhuo, C.; Jiang, D. Validity and Reliability of a Chinese Version of the Self-Evaluation of Negative Symptoms. Brain Behav 2023, 13, e2924. https://doi.org/10.1002/brb3.2924. [CrossRef]
  42. Goldring, A.; Borne, S.; Hefner, A.; Thanju, A.; Khan, A.; Lindenmayer, J.-P. The Psychometric Properties of the Self-Evaluation of Negative Symptoms Scale (SNS) in Treatment-Resistant Schizophrenia (TRS). Schizophrenia Research 2020, 224, 159–166. https://doi.org/10.1016/j.schres.2020.08.008. [CrossRef]
  43. Hervochon, C.; Bourgeois, V.; Rotharmel, M.; Duboc, J.-B.; Le Goff, B.; Quesada, P.; Campion, D.; Dollfus, S.; Guillin, O. [Validation of the French version of the self-evaluation of negative symptoms (SNS)]. Encephale 2018, 44, 512–516. https://doi.org/10.1016/j.encep.2017.10.002. [CrossRef]
  44. Wójciak, P.; Górna, K.; Domowicz, K.; Jaracz, K.; Gołębiewska, K.; Michalak, M.; Rybakowski, J. Polish Version of the Brief Negative Symptom Scale (BNSS). Psychiatr Pol 2019, 53, 541–549. https://doi.org/10.12740/PP/OnlineFirst/91490. [CrossRef]
  45. García-Álvarez, L.; Martínez-Cao, C.; Bobes-Bascarán, T.; Portilla, A.; Courtet, P.; de la Fuente-Tomás, L.; Velasco, Á.; González-Blanco, L.; Zurrón-Madera, P.; Fonseca-Pedrero, E.; et al. Validation of a European Spanish-Version of the Self-Evaluation of Negative Symptoms (SNS) in Patients with Schizophrenia. Rev Psiquiatr Salud Ment (Engl Ed) 2020, S1888-9891(20)30036-7. https://doi.org/10.1016/j.rpsm.2020.04.011. [CrossRef]
  46. Mazhari, S.; Karamooz, A.; Shahrbabaki, M.E.; Jahanbakhsh, F.; Dollfus, S. Validity and Reliability of a Persian Version of the Self- Evaluation of Negative Symptoms (SNS). BMC Psychiatry 2021, 21, 516. https://doi.org/10.1186/s12888-021-03521-7. [CrossRef]
  47. García-Álvarez, L.; Martínez-Cao, C.; Bobes-Bascarán, T.; Portilla, A.; Courtet, P.; de la Fuente-Tomás, L.; Velasco, Á.; González-Blanco, L.; Zurrón-Madera, P.; Fonseca-Pedrero, E.; et al. Validation of a European Spanish-Version of the Self-Evaluation of Negative Symptoms (SNS) in Patients with Schizophrenia. Rev Psiquiatr Salud Ment (Engl Ed) 2022, 15, 14–21. https://doi.org/10.1016/j.rpsmen.2022.01.005. [CrossRef]
  48. Dollfus, S.; Mucci, A.; Giordano, G.M.; Bitter, I.; Austin, S.F.; Delouche, C.; Erfurth, A.; Fleischhacker, W.W.; Movina, L.; Glenthøj, B.; et al. European Validation of the Self-Evaluation of Negative Symptoms (SNS): A Large Multinational and Multicenter Study. Front. Psychiatry 2022, 13, 826465. https://doi.org/10.3389/fpsyt.2022.826465. [CrossRef]
  49. Tam, M.H.W.; Ling-Ling, W.; Cheng, K.; Wong, J.O.Y.; Cheung, E.F.C.; Lui, S.S.Y.; Chan, R.C.K. Latent Structure of Self-Report Negative Symptoms in Patients with Schizophrenia: A Preliminary Study. Asian Journal of Psychiatry 2021, 61, 102680. https://doi.org/10.1016/j.ajp.2021.102680. [CrossRef]
  50. Mallet, J.; Guessoum, S.B.; Tebeka, S.; Le Strat, Y.; Dubertret, C. Self-Evaluation of Negative Symptoms in Adolescent and Young Adult First Psychiatric Episodes. Progress in Neuro-Psychopharmacology and Biological Psychiatry 2020, 103, 109988. https://doi.org/10.1016/j.pnpbp.2020.109988. [CrossRef]
  51. Métivier, L.; Mauduy, M.; Beaunieux, H.; Dollfus, S. Revealing the Unseen: Detecting Negative Symptoms in Students. JCM 2024, 13, 1709. https://doi.org/10.3390/jcm13061709. [CrossRef]
  52. Hajj, A.; Hallit, S.; Chamoun, K.; Sacre, H.; Obeid, S.; Haddad, C.; Dollfus, S.; Rabbaa Khabbaz, L. Validation of the Arabic Version of the “Self-Evaluation of Negative Symptoms” Scale (SNS). BMC Psychiatry 2020, 20, 240. https://doi.org/10.1186/s12888-020-02647-4. [CrossRef]
  53. Wójciak, P.; Górna, K.; Domowicz, K.; Jaracz, K.; Szpalik, R.; Michalak, M.; Rybakowski, J. Polish Version of the Self-Evaluation of Negative Symptoms (SNS). Psychiatr Pol 2019, 53, 551–559. https://doi.org/10.12740/PP/OnlineFirst/97352. [CrossRef]
  54. Haro, J.M.; Kamath, S.A.; Ochoa, S.; Novick, D.; Rele, K.; Fargas, A.; Rodríguez, M.J.; Rele, R.; Orta, J.; Kharbeng, A.; et al. The Clinical Global Impression-Schizophrenia Scale: A Simple Instrument to Measure the Diversity of Symptoms Present in Schizophrenia. Acta Psychiatr Scand Suppl 2003, 16–23. https://doi.org/10.1034/j.1600-0447.107.s416.5.x. [CrossRef]
  55. Kirkpatrick, B.; Saoud, J.B.; Strauss, G.P.; Ahmed, A.O.; Tatsumi, K.; Opler, M.; Luthringer, R.; Davidson, M. The Brief Negative Symptom Scale (BNSS): Sensitivity to Treatment Effects. Schizophr Res 2018, 197, 269–273. https://doi.org/10.1016/j.schres.2017.11.031. [CrossRef]
  56. Axelrod, B.N.; Goldman, R.S.; Alphs, L.D. Validation of the 16-Item Negative Symptom Assessment. J Psychiatr Res 1993, 27, 253–258. https://doi.org/10.1016/0022-3956(93)90036-2. [CrossRef]
  57. Rodríguez-Testal, J.F.; Perona-Garcelán, S.; Dollfus, S.; Valdés-Díaz, M.; García-Martínez, J.; Ruíz-Veguilla, M.; Senín-Calderón, C. Spanish Validation of the Self-Evaluation of Negative Symptoms Scale SNS in an Adolescent Population. BMC Psychiatry 2019, 19, 327. https://doi.org/10.1186/s12888-019-2314-1. [CrossRef]
  58. Gard, D.E.; Gard, M.G.; Kring, A.M.; John, O.P. Anticipatory and Consummatory Components of the Experience of Pleasure: A Scale Development Study. Journal of Research in Personality 2006, 40, 1086–1102. https://doi.org/10.1016/j.jrp.2005.11.001. [CrossRef]
  59. Raffard, S.; Norton, J.; Van der Linden, M.; Lançon, C.; Benoit, M.; Capdevielle, D. Psychometric Properties of the BIRT Motivation Questionnaire (BMQ), a Self-Measure of Avolition in Individuals with Schizophrenia. Journal of Psychiatric Research 2022, 147, 274–282. https://doi.org/10.1016/j.jpsychires.2022.01.033. [CrossRef]
  60. Tsui, H.K.H.; Wong, T.Y.; Sum, M.Y.; Chu, S.T.; Hui, C.L.M.; Chang, W.C.; Lee, E.H.M.; Suen, Y.; Chen, E.Y.H.; Chan, S.K.W. Comparison of Negative Symptom Network Structures Between Patients With Early and Chronic Schizophrenia: A Network and Exploratory Graph Analysis. Schizophr Bull 2024, sbae135. https://doi.org/10.1093/schbul/sbae135. [CrossRef]
  61. Strauss, G.P.; Ahmed, A.O.; Young, J.W.; Kirkpatrick, B. Reconsidering the Latent Structure of Negative Symptoms in Schizophrenia: A Review of Evidence Supporting the 5 Consensus Domains. Schizophrenia Bulletin 2018, 45, 725. https://doi.org/10.1093/schbul/sby169. [CrossRef]
  62. Li, Y.; Ang, M.S.; Yee, J.Y.; See, Y.M.; Lee, J. Predictors of Functioning in Treatment-Resistant Schizophrenia: The Role of Negative Symptoms and Neurocognition. Front Psychiatry 2024, 15, 1444843. https://doi.org/10.3389/fpsyt.2024.1444843. [CrossRef]
  63. Mortimer, A.M.; McKenna, P.J.; Lund, C.E.; Mannuzza, S. Rating of Negative Symptoms Using the High Royds Evaluation of Negativity (HEN) Scale. Br J Psychiatry Suppl 1989, 89–92.
  64. Torous, J.; Bucci, S.; Bell, I.H.; Kessing, L.V.; Faurholt-Jepsen, M.; Whelan, P.; Carvalho, A.F.; Keshavan, M.; Linardon, J.; Firth, J. The Growing Field of Digital Psychiatry: Current Evidence and the Future of Apps, Social Media, Chatbots, and Virtual Reality. World Psychiatry 2021, 20, 318–335. https://doi.org/10.1002/wps.20883. [CrossRef]
  65. Wang, L.; Miller, L.C. Just-in-the-Moment Adaptive Interventions (JITAI): A Meta-Analytical Review. Health Communication 2020, 35, 1531–1544. https://doi.org/10.1080/10410236.2019.1652388. [CrossRef]
Figure 1. Flow-shart.
Figure 1. Flow-shart.
Preprints 143286 g001
Table 1. General characteristics of self-assessment scales with more than 2 negative symptom domains.
Table 1. General characteristics of self-assessment scales with more than 2 negative symptom domains.

Scale
Population Mean Age (SD) Gender(female %) Countries
validation
Negative Symptoms
domains
Number of items Duration
Subjective Experience of Negative Symptoms (SENS)
Selten et al., 1993 [25]


52 patients with schizophrenia


39.5 (10.8)


34.6


Netherlands
Anhedonia/asociality
Avolition/apathy
Affective flattening
Alogia
Attention
21 -
Clinical Assessment Interview for Negative Symptoms Self-Report (CAINS-SR)


Park et al., 2020 [26]



41 patients with schizophrenia32 patients with schizo-affective disorders



47.1 (8.36)



36.2



North America
Anhedonia
Avolition
Alogia
Blunted affect
Asociality
30 -
Motivation And Pleasure Scale
Self-Report (MAPS-SR)


Llerena et al., 2013 [16]

Engel et al., 2016 [30]

Wang et al., 2020 [28]

Kim et al., 2016 [33]

Richter et al., 2019 [29]

Garcia-Portilla et al., 2021 [31]

Cernvall et al., 2024 [32]


37 patients with schizophrenia or schizo-affective disorders
50 patients with schizophrenia or schizo-affective disorders
150 patients with schizophrenia
139 patients with schizophrenia
93 patients with schizophrenia or schizo-affective disorder
174 patients with schizophrenia
33 patients with schizophrenia spectrum disorders


50.16 (5.12)
35.70 (10.36)
46.47 (8.37)
38.9 (11.1)
38.99 (10.99)
36.7 (12.2)
40.0 (11.0)


35.1
44
51.3
45.3
33.3
37.4
36


North America
Germany
China
Korea
German
Spain
Sweden
Anhedonia
Avolition
Social withdrawal
15 -
Self-evaluation of Negative Symptoms (SNS)


Dollfus et al., 2016 [15]


Hervochon et al., 2018 [43]


Wojciak et al., 2019 [44]


Dollfus et al., 2019 [9]


Hajj et al., 2019 [37]

Mallet et al., 2020 [50]




Garcia-Alvarez et al., 2020 [45]

Goldring et al., 2020 [42]

Tam et al., 2021 [49]

Montvidas et al., 2021 [38]

Mazhari et al., 2021 [46]

Garcia-Alvarez et al., 2022 [47]

Polat et al., 2022 [39]
Dollfus et al., 2022 [48]

Samochowiec et al., 2023 [40]

Chen et al., 2023 [41]

Métivier et al, 2024 [51]


23 patients with schizophrenia
26 patients with schizo-affective disorders
60 patients with schizophrenia or schizo-affective disorders
40 patients with schizophrenia
109 patients with schizophrenia or schizo-affective disorders
99 healthy controls
206 patients with schizophrenia
29 patients with schizophrenia
22 patients with depressive disorder
59 healthy controls
104 patients with schizophrenia
50 patients with resistant schizophrenia
204 patients with schizophrenia
67 patients with schizophrenia
50 patients with schizophrenia
104 patients with schizophrenia
75 patients with schizophrenia
245 patients with schizophrenia
82 patients with schizophrenia
200 patients with schizophrenia
367 students with ultra-high risk of psychosis or major depressive disorders
1761 healthy students


36.7 (11.6)

40.6 (10.7)
44.0 (13.0)
38.9 (11.3)
28.8 (13.2)
52.68 (12.0)
19.4 (3.0)
18.0 (2.0)
20.4 (2.8)
40.1 (13.9)
43.8 (11.19)
49.36 (10.23)
41.51 (13.76)
39.5 (11.1)
40.1 (13.9)
21.91 (5.44)
37.4 (11.3)
NR
35.2 (3.9)
NR
NR


20.4

20
50
NR
NR
56.8
36.8
59.1
62.7
35.6
12
51.47
64.2
32
35.6
36
37
NR
53.5
NR
NR
27 languages
(www.sns-dollfus.com/fr
France

France
Poland
France
Lebanon
France

Spain
North America
Hong-Kong and China
Lithuania
Iran
Spain
Turkey
European countries
Poland
China
France
Anhedonia
Avolition
Alogia
Reduced emotional range
Social withdrawal
20 5 min
Negative Symptoms Inventory Self-Report (NSI-SR)

Raugh et al., 2023 [24]


32 patients with schizophrenia or schizo-affective disorders
25 patients with clinical high-risk of psychosis


40.12 (13.25)
41.32 (9.43)


75
83.9


North America
Anhedonia
Avolition
Social withdrawal
11 Few minutes
* SD: Standard Deviation.
Table 2. COSMIN criteria of self-assessment scales with more than 2 negative symptom domains.
Table 2. COSMIN criteria of self-assessment scales with more than 2 negative symptom domains.
SENS [25]
Measurement property
(no, of study assessing measurement property)

Cosmin risk of bias

Update criteria of good measurement
Very good Adequate Doubtful Inadequate + - ?
Structural validity
(n = 0)
0 0 0 0 0 0 0
Internal consistency
(n = 1)
0 0 1 0 0 0 1
Reliability
(n = 1)
0 1 0 0 0 1 0
Criterion validity (n = 0) 0 0 0 0 0 0 0
Hypotheses testing for construct validity convergent validity
(n = 0)
0 0 0 0 0 0 0
Hypotheses testing for construct validity discriminant validity (n = 0) 0 0 0 0 0 0 0
Quality of evidence (GRADE) Very Low
Recommendation C
CAINS-SR [26]
Measurement property
(no, of study assessing measurement property)

Cosmin risk of bias

Update criteria of good measurement
Very good Adequate Doubtful Inadequate + - ?
Structural validity
(n = 0)
0 0 0 0 0 0 0
Internal consistency
(n = 1)
0 0 1 0 0 0 1
Reliability
(n = 0)
0 0 0 0 0 0 0
Criterion validity 0 0 0 0 0 0 0
Hypotheses testing for construct validity convergent validity
(n = 1)
0 1 0 0 1 0 0
Hypotheses testing for construct validity discriminant validity (n = 1) 0 1 0 0 1 0 0
Quality of evidence (GRADE) Very Low
Recommendation C
MAP-SR [16,28,29,30,31,32,33]
Measurement property
(no, of study assessing measurement property)

Cosmin risk of bias

Update criteria of good measurement
Very good Adequate Doubtful Inadequate + - ?
Structural validity
(n = 2) [28,29]
1 0 1 0 1 1 0
Internal consistency
(n = 7) [16,28,29,30,31,32,33]
2 0 5 0 2 0 5
Reliability
(n = 2) [28,29]
0 2 0 0 1 1 0
Criterion validity (n = 0) 0 0 0 0 0 0 0
Hypotheses testing for construct validity convergent validity
(n = 7) [16,28,29,30,31,32,33]
2 5 0 0 6 1 0
Hypotheses testing for construct validity discriminant validity
(n = 7) [16,28,29,30,31,32,33]
2 5 0 0 4 0 3
Quality of evidence (GRADE) Moderate
Recommendation A
SNS [9,15,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51]
Measurement property
(no, of study assessing measurement property)

Cosmin risk of bias

Update criteria of good measurement
Very good Adequate Doubtful Inadequate + - ?
Structural validity
(n = 9) [15,37,38,39,40,41,42,48,49]
3 0 1 5 8 0 1
Internal consistency
(n = 12) [15,37,38,39,40,41,42,43,44,45,46,47]
1 0 11 0 4 2 6
Reliability (n = 4)
[15,37,42,43]
2 1 0 1 2 1 1
Criterion validity (n = 5) [9,40,41,50,51] 5 0 0 0 5 0 0
Hypotheses testing for construct validity convergent validity
(n = 13) [15,37,38,39,40,41,42,43,44,45,46,47,48]
8 5 0 0 12 1 0
Hypotheses testing for construct validity discriminant validity
 (n = 9) [15,38,39,42,43,45,47,48,52]
3 4 2 0 7 0 2
Quality of evidence (GRADE) Moderate
Recommendation A
NSI-SR [24]
Measurement property
(no, of study assessing measurement property)

Cosmin risk of bias

Update criteria of good measurement
Very good Adequate Doubtful Inadequate + - ?
Structural validity
(n = 1)
1 0 0 0 1 0 0
Internal consistency
(n = 1)
1 0 0 0 1 0 0
Reliability
(n = 1)
0 1 0 0 0 1 0
Criterion validity (n = 0) 0 0 0 0 0 0 0
Hypotheses testing for construct validity convergent validity
(n = 1)
1 0 0 0 0 1 0
Hypotheses testing for construct validity discriminant validity (n = 1) 1 0 0 0 0 1 0
Quality of evidence (GRADE) Low
Recommendation B
* +: criterion validated; -: criterion not validated; ?: indeterminate. * CAINS-SR: Clinical Assessment Interview Negative Symptoms Self-Report); GRADE: Grading of Recommendations Assessment, Development, and Evaluation; MAPS-SR: Motivation And Pleasure Scale Self-Report; Negative Symptoms Inventory Self-Report (NSI-SR); SENS: Subjective Experience of Negative Symptoms; SNS: Self-evaluation of Negative Symptoms.
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