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NCT06816693Completed

Exploratory Study of the Usability, Feasibility, and Perception for Tele-cardiac Rehabilitation (Tele-CR) Program

Feasibility Study of a Mobile Application (App)-Based Tele-cardiac Rehabilitation (Tele-CR) Program for Patients With Coronary Heart Disease (CHD): Mixed Methods

Source: ClinicalTrials.gov · Last updated 20 Mar 2026

Brief summary (registry, in English)

The goal of this mixed prospective observational and qualitative studies is to evaluate the usability of a newly developed application (App) and the feasibility and perception of a 12 weeks tele-cardiac rehabilitation (tele-CR) program. The main question it aims to answer is: Does tele-CR program intervention a acceptance feasibility in coronary heart disease patients? The findings will guide subsequent intervention design studies.

Status (registry)
Completed
Study type
Observational
Enrollment
34 (actual)
First submitted
22 Jan 2025
Start date
31 Mar 2025
Primary completion date
31 Jan 2026
Lead sponsor
Chang Gung University of Science and Technology
NCT number
NCT06816693

What you commit to

  • Study type: Observational
  • Participants enrolled: 34
  • From 31 Mar 2025 to the primary completion date, 31 Jan 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Planning to receive surgery (e.g., coronary artery bypass graft).

Other illness

  • Level IV on the New York Heart Association Functional Classification.
  • Have a history of severe arrhythmia (e.g., ventricular tachycardia, ventricular fibrillation, complete atrioventricular block).
  • Combined with other serious heart diseases (e.g., congenital heart disease, cardiomyopathy).
  • Mental disorders, end-stage renal disease and other systemic diseases diagnosed by a physician.
  • Severe infection, injury, surgery (e.g., coronary artery bypass graft) or cancer treatment has occurred in the past three months.
  • Physical activities are affected by neurological, respiratory, skeletal, or peripheral vascular diseases.
  • Restricted use of the App due to sensory or cognitive impairment.

Lab values

  • Left ventricular ejection fraction≦40%.

Other

  • Already participated in other clinical trials.

Who the study is looking for

  • The main diagnosis at admission of CHD.
  • Age ≥20 years.
  • Owns an iOS or Android smartphone and can use it.
  • Conscious, clear and can communicate.
  • Agrees to participate in the research after explanation and is willing to use the App.

Age in the registry: 20 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Chang Gung Memorial Hospital
Coordinator of this site? Confirm its status
TaoyuanTaiwanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.