NCT07030335Not yet recruiting
Evaluation of Mobile Education Program in Patients With Atrial Fibrillation.
The Effect Of A Mobıle Educatıon Program and Telephone Follow-Up On Knowledge Level, Symptom Management And Qualıty Of Lıfe In Patıents Wıth Atrıal Fıbrıllatıon
Source: ClinicalTrials.gov · Last updated 22 Jun 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
This study was conducted to determine the effect of a mobile education program and telephone follow-up on the knowledge level, symptom management and quality of life of patients with atrial fibrillation. The study aims to answer the following questions. 1. Does the mobile education program and telephone follow-up have an effect on increasing the level of knowledge in patients with AF in the intervention group compared to the control group? 2. Does the mobile education program and telephone follow-up have an effect on reducing symptom severity in patients with AF in the intervention group compared to the control group? 3. Does the mobile education program and telephone follow-up have an effect on improving the quality of life in patients with AF in the intervention group compared to the control group?
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 70 (estimated)
- First submitted
- 27 May 2025
- Start date
- Jun 2025
- Primary completion date
- Jul 2025
- Lead sponsor
- Akdeniz University
- Diseases
- Atrial fibrillation
- NCT number
- NCT07030335
What you commit to
- Study type: Interventional
- Planned participants: 70
- From Jun 2025 to the primary completion date, Jul 2025
- 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
- Diagnosis of rheumatic valve disease, moderate/severe mitral stenosis and previous valve surgery.
Other illness
- Functional class III or IV according to the New York Heart Association (NYHA) classification.
Other
- Patients with existing or planned pacemaker, ICD (Implantable Cardioverter Defibrillator) and patients with existing or planned Radiofrequency Ablation treatment will not be included in the study.
Who the study is looking for
- 18 years of age or older.
- Being literate.
- Atrial Fibrillation diagnosis.
- No cognitive and communication disabilities.
- Not having a diagnosed psychiatric illness.
- Ability to use technological devices.
- Having and using a smart phone with Android operating system and internet access.
- Acceptance to participate in the study.
Age in the registry: 18 years to - · 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 |
|---|---|---|---|
| Akdeniz University Hospital Cardiology Polyclinic Coordinator of this site? Confirm its status | Antalya | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.