Can a smartphone app help heart patients recover at home?
NCT ID NCT06816693
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a 12-week mobile app program for heart rehab is practical and liked by patients with coronary heart disease. 34 adults used the app after leaving the hospital, and researchers tracked how many signed up, used the app, and stayed in the program. The goal was to see if this approach is worth studying further, not to measure health outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- tele-CR program (behavioral intervention via mobile app)
- What this could lead to
- If successful, this could pave the way for a larger trial testing whether app-based rehab improves heart health outcomes.
- What could go wrong
- This is a small, early feasibility study with only 34 participants, so results may not apply to all heart patients. It does not measure actual health improvements.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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34 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Jan 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients admitted to the hospital with a primary diagnosis of CHD will be conducted. We plan to recruit a group of patients to receive the tele-CR program and evaluate the usability of the App perceived by patients at 1 and 3 months after discharge. Therefore, we use the t-test (one sample case) statistical method and set the effect size to a moderate 0.5, power is 0.8, alpha is 0.05 (two-tailed), and the number of samples required after calculation using G\*power 3.1 software is 34. Considering the 20% attrition rate, we estimate that we will recruit 45 cases (quantitative). The number of samples for qualitative research is mainly to achieve data saturation, and according to the literature, it is recommended to have at least 12 people.
- Ages
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20 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. The main diagnosis at admission of CHD. 2. Age ≥20 years. 3. Owns an iOS or Android smartphone and can use it. 4. Conscious, clear and can communicate. 5. Agrees to participate in the research after explanation and is willing to use the App. Exclusion Criteria: 1. Level IV on the New York Heart Association Functional Classification. 2. Left ventricular ejection fraction≦40%. 3. Have a history of severe arrhythmia (e.g., ventricular tachycardia, ventricular fibrillation, complete atrioventricular block). 4. Combined with other serious heart diseases (e.g., congenital heart disease, cardiomyopathy). 5. Mental disorders, end-stage renal disease and other systemic diseases diagnosed by a physician. 6. Severe infection, injury, surgery (e.g., coronary artery bypass graft) or cancer treatment has occurred in the past three months. 7. Physical activities are affected by neurological, respiratory, skeletal, or peripheral vascular diseases. 8. Restricted use of the App due to sensory or cognitive impairment. 9. Already participated in other clinical trials. 10. Planning to receive surgery (e.g., coronary artery bypass graft).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Chang Gung Memorial Hospital
Taoyuan, Guishan Dist., 333, Taiwan
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