NCT06240702Completed
Effects of Early Telerehabilitation in Coronary Artery Bypass Surgery Patients
The Effect of Early Cardiopulmonary Telerehabilitation on Exercise Capacity, Cardiac Function, Quality of Life and Emotional Status in Coronary Bypass Surgery Patients
Source: ClinicalTrials.gov · Last updated 12 Nov 2024
Brief summary (registry, in English)
The aim of this study was to investigate the effects of phase I and early phase II rehabilitation with telerehabilitation method and sleep hygiene training on physical capacity, cardiac functions, anxiety level, quality of life and sleep quality in patients undergoing coronary artery bypass graft surgery.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 40 (actual)
- First submitted
- 26 Jan 2024
- Start date
- 20 Apr 2024
- Primary completion date
- 20 Aug 2024
- Lead sponsor
- Necmettin Erbakan University
- Diseases
- Coronary artery disease
- NCT number
- NCT06240702
What you commit to
- Study type: Interventional
- Participants enrolled: 40
- From 20 Apr 2024 to the primary completion date, 20 Aug 2024
- 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.
Other illness
- Patients with neurological orthopedic comorbid diseases
- Patients with Chronic Obstructive Pulmonary Disease (COPD)
Other
- Aneurysm history
- Patients with advanced left ventricular dyskinesia
- Presence of any defect in the rib cage
- Patients hospitalized for a long time (6 months and more)
Who the study is looking for
- Participants who are class 2-3 according to the New York Heart Association (NYHA)
- Participants had an ejection fraction \>40%
- If the participant has had a myocardial infarction (MI), 7 days have passed since the MI
- Low-medium risk group patients as a result of Euroscore evaluation (0-2 low risk, 3-5 medium risk, 6\< high)
- Patients with adequate cognition-perception level (Mini mental test score of 24 and above)
- Individuals who are not diagnosed with sleep disorders for any reason
- Having the knowledge to make video calls with a smart phone
- Declaring that you wish to participate in the study with written consent
Age in the registry: 45 years to 75 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 |
|---|---|---|---|
| Necmettin Erbakan University, Faculty of Medicine Coordinator of this site? Confirm its status | Konya | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.