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education video / Heart Failure / Bradycardia · Interventional Study
ClinicalTrials.gov · September 9, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a completed single-centre randomized controlled trial testing whether video-based cardiac rehabilitation education improves device-measured physical activity in patients with cardiac implantable electronic devices (CIEDs), comparing intervention to standard health education. No results have been posted to the registry, so the efficacy and safety of the intervention remain unreported.
Interventional, Randomized, Parallel, Double masking, Prevention purpose. Bradycardia, Arrhythmia, Heart Failure; age from 20 Years; to 100 Years. Intervention: Cardiac rehabilitation. Compared with: general health — Sham Comparator. n = 85. 1 site: Taiwan.
This is a completed single-centre randomized controlled trial testing whether video-based cardiac rehabilitation education improves device-measured physical activity in patients with cardiac implantable electronic devices (CIEDs), comparing intervention to standard health education. No results have been posted to the registry, so the efficacy and safety of the intervention remain unreported.
Results are not posted in this registry record; no efficacy or safety data are available to evaluate. Physical activity is a surrogate endpoint; clinical outcomes (mortality, hospitalization, quality of life) are not primary outcomes.
The source did not state who this applies to in practice.
This is a completed but unpublished registry record for a small, single-centre RCT with a surrogate endpoint (device-measured physical activity); results are not yet reported.
As stated by the source record.
Quoted from the source exactly as published.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT06503445). This is a study registration, not published results. Lead sponsor: National Taiwan University Hospital Hsin-Chu Branch. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 85 participants (ACTUAL). Conditions: Bradycardia, Arrhythmia, Heart Failure. Interventions: OTHER: education video. Primary outcome measures: Device measurement: physical activity , We collected data on the day of case enrollment and twelve weeks later.. Brief summary: Cardiac rehabilitation has the beneficial effects of secondary prevention and social psychological and physical health status in patients with cardiovascular diseases. International and clinical guidelines currently recommend exercise training and rehabilitation for heart failure patients, which can effectively improve mortality and prognosis. However, few of these recommendations have specific recommendations for patients with cardiac implantable electronic devices. Currently the recommendations of cardiac rehabilitation include patients with coronary heart disease (acute coronary heart disease, any coronary revascularization, stable coronary disease or unstable angina), patients with heart failure, after cardiac surgery, and patients with high cardiovascular risk. Many of these patients may be implanted with cardiac implantable electronic devices. In 2011, 938 pacemakers, 140 cardiac resynchronization therapy and 149 implantable cardioverter defibrillators were implanted per million inhabitants in Europe. Therefore, among the groups with cardiac implantable electronic devices, cardiac rehabilitation plays a certain role. The purpose of this study is to evaluate whether video-based cardiac rehabilitation health education for patients with cardiac implantable electronic devices has significantly improved physical activity. This study is designed as a prospective, single center, double-blind, randomized controlled trial. Divided into an experimental group and a control group at a ratio of 1:1. The experimental group with cardiac implantable electronic devices will receive cardiac rehabilitation health education video intervention, and the control group will receive only health education. We aim to recruit 45 participants per group with a total of 90 participants.
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.