NCT07808307Not yet recruiting
Tele-Rehabilitation After Catheter Ablation in Patients With Atrial Fibrillation
Effects of Remotely Supervised Cardiac Tele-Rehabilitation in Patients With Atrial Fibrillation After Catheter Ablation: A Single-Blind Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 8 Sept 2026
Brief summary (registry, in English)
This study aims to investigate the effects of remotely supervised cardiac telerehabilitation in patients with atrial fibrillation who have undergone catheter ablation. Participants will be randomly assigned to a cardiac telerehabilitation group or a control group. The telerehabilitation group will receive a 12-week remotely supervised exercise program in addition to standard care, consisting of aerobic, strengthening, and stretching exercises. The control group will receive standard care and general exercise guidance without an individualized exercise program. Functional exercise capacity, muscle strength, arterial stiffness, heart rate variability, quality of life, physical activity, balance, cognitive function, anxiety and depression, and atrial fibrillation recurrence will be evaluated.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 28 (estimated)
- First submitted
- 27 Aug 2026
- Start date
- 1 Sept 2026
- Primary completion date
- 30 Jun 2027
- Lead sponsor
- Hande Cörüt
- Diseases
- Atrial fibrillation
- NCT number
- NCT07808307
What you commit to
- Study type: Interventional
- Planned participants: 28
- From 1 Sept 2026 to the primary completion date, 30 Jun 2027
- 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, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Acute heart failure, cancer, or worsening of a comorbid condition within the previous 3 months that may affect the assessment or intervention.
Other illness
- Presence of a non-cardiovascular condition (orthopedic or neurological) that limits participation in exercise.
- Severe cognitive impairment.
Other
- Unwillingness to participate in the study.
Who the study is looking for
- Aged 50-75 years.
- Diagnosed with atrial fibrillation and treated with catheter ablation.
- Have a smartphone or computer compatible with the digital equipment provided for the study.
- Have access to the Internet.
- Provide written informed consent to participate in the study.
Age in the registry: 50 years to 70 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Dokuz Eylul University Hospital Coordinator of this site? Confirm its status | Izmir | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.