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A peer-reviewed article of this preprint also exists.
This version is not peer-reviewed
Submitted:
29 August 2024
Posted:
30 August 2024
You are already at the latest version
Article | Sample(n) | Type of study | Intervention and patient information | Summary |
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|
1424 | Randomized control trial (RCT) |
1424 patients (mean age=58 years, 79% male) with heart disease ( from 18 Australian teaching hospitals), owning a text capable, mobile phone, with the ability to read messages in English, were followed for a year. The participants were compared to a control group, with no text messages. | The program delivered consistent education and support to cardiac patients after hopitalization. Results showed favorable response from patients, including high levels of acceptability, usefulness in being a unified source of information, program engagement, and emotional support. However medication adherence was not improved. |
|
13 | Observational study | 13 participants (1 female) mean age=63, with cardiac surgery, angina or heart failure, owning a mobile phone or computer with internet access, participated in this study related to feedback of Veteran use of a mobile application. The mobile app VA FitHeart, included health education along with reminders and feedback. The app also provided physical activity goal setting, alongwith daily logs for physical activity tracking and health metrics recording(e.g., blood pressure, weight and mood/ emotional well-being) | The study used patients feedback to improve the usability of the app, through questionnaitres and semistructured interviews. Patient expectations for using a mobile app for Cardiac rehabilitation (CR) included tracking health metrics, introductory training, and sharing data with providers. Patients in the study desired the ability to track physical activity. |
|
258 | Open label trial | Patients with cardiac disease were required to own an Android or an iOS smartphone in working condition with access to Wi-Fi or a data plan to enroll in this digital health intervention (DHI) program for the cardiac rehabilitation program at the VHA medical center. A total of 258 participants mean age 60+9 yrs, 93% male and 48% blacks, enrolled in the program for three months. | Results indicated that the remote CR with DHI was feasible in the VA hospital setting. Participants health status improved with better walking capabilities and low density lipoprotein cholesterol, while smoking decreased. Additionally, no adverse events were noted. |
|
113 | RCT | 113 patients completing cardiac rehab, were randomly allocated to the intervention. Mean age of particpants= 59, 22% females ( coronary artery disease= 73.4%, 16.8%= valve surgery, and other heart diseases= 9.8%). The intervention consisted of receiving follow up with the m-health app or a control group with usual care. Patients were recruited from two CR centers in the eastern region of Norway. | Post-CR patients were compared with control group in this study consisting of individualized follow up for one year with an app. Improvements were seen in VO2peak, exercise performance and exercise habits, as well as self-perceived goal achievement. No other outcomes were different. |
|
268 | Descriptive mixed methods study | The questionnaire was distributed among 268 patients attending an outpatient arrhythmia clinic. 82.4 % men with mean age 69 years, participated in this study conducted in Northern, Italy. |
In this study the results indicate that the patients expressed a greater interest in receiving information related to the effectivenes and integrity of the device. Lower interest towards the clinical status and arrythmic episodes and healthy lifestyle counselling was observed. |
|
40 | Community participatory research design | 40 Black women aged 25-45 years with at least two cardiovascular risk factors, completed 4 sessions of cardiovascular disease risk reduction education as well as a 6-month smartphone coaching and cardiovascular disease risk reduction monitoring, which targeted heart healthy lifestyle and behavior modifications. | The results indicate that m-Health intervention was a feasible tool for implemeting cardiovascular disease risk reduction for young black women. Imrpoving the health awareness of the participants had indirect benefits for other family members especially children. |
|
32 | RCT | The impact of HeartHab app was studied on 32 coronary artery disease patients for 4 months, in Belgium. Overall patients motivation, physical activity, exercise target achievement, quality of life and modifiable risk factors were investigated. | Results demonstated positive improvements in VO2 max, glucose, HDL cholesterol, weight and quality of life. |
|
48 | RCT | 48 participants (46% women, 58 years age mean) from a cardiology center in Baltimore, owning smartphones, took part in this study for 4 months with the objective that mHealth intervention with tracking and texting components would increase physical activity. | Smart texts with activity tracking led to the best physical activity outcomes, such as increased daily steps(better outcomes than tracking only). |
|
14 | Clinical trial (pilot study) | 14 (8-19 year old) patients (at least 1 year postcardiac transplant surgery) underwent a 12- 16 week diet and exercise intervention which was delivered via live video conferencing to improve cardiovascular health. | Results indicate that the lifestyle intervention of exercise and nutrition was feasible with excellent adherence, improvements in cardiac,vascular, nutritional and functional health. |
|
24 | Cohort study | 24 patients with Marfan syndrome (8 to 19 years old) participated in a 6-month physical activity intervention and their steps were tracked. | Physical activity intervention was feasible in this population and has the potential to decrease the aortic root (AoR) dilation rate. |
|
12 | Feasibility study | Mean age of participants was 15.4 years (SD = 3.4) with mean time since cardiac transplant of 9.7 years (SD= 4.3). Participants wore a FitBit accelerometer throughout the duration of the study to monitor daily activity levels. The participants underwent the intervention for 16 weeks, which consisted of exercise sessions twice a week for 30 mins, supervised by a trained exercise physiologist over a virtual platform. At the conclusion of the intervention participants repeated the strength and flexibility assessment, a 6MWT and quality of life (QoL) parameters measurement to compare with baseline. |
Results of the study indicate the successful implementaton of a virtual cardiac fitness intervention with improvement in QoL metrics and excellent adherence of participants. |
Chow et al | Beatty et al | Harzand et al |
Lunde et al | Villani et al | Kathuria-Prakash et al |
Sankaran et al | Martin et al | Chen et al | Tiernay et al | Ziebell et al | |
---|---|---|---|---|---|---|---|---|---|---|---|
Study purpose: was the purpose stated clearly? |
Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Literature: was relevant and background literature reviewed? |
Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Design |
RCT | Observational study | Open label trial | RCT | Descriptive mixed methods study | Community participatory research design | RCT | RCT | Open label trial | Cohort | Feasibility study |
Sample | N=1424 | N=13 |
N=258 |
N= 113 | N= 268 | N=40 |
N=32 |
N=48 |
N=14 | N=24 | N=12 |
Was the sample described in detail? |
Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Was the sample size justified? |
Yes | No | No | Yes | No | No | Yes | Yes | Yes | No | No |
Results: Results were reported in terms of statistical significance. |
Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Were the analysis method(s) appropriate? |
Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Clinical importance was reported? |
Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Drop-outs were reported? |
Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Conclusions and clinical implications: Conclusions were appropriate given the study methods and results |
Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
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