Trials / Completed
CompletedNCT06970938
Cardiac Rehabilitation After Coronary Artery Bypass Graft Surgery
Effect of Cardiac Rehabilitation Program on Quality of Life, Sleep Quality, Anxiety, Depression and Cardiopulmonary Function After Coronary Artery Bypass Graft Surgery: a Randomized Controlled Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 28 (actual)
- Sponsor
- Muhammed Onur Hanedan · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study aimed to evaluate the effects of cardiac rehabilitation program after CABG surgery on quality of life, sleep quality, anxiety, depression and cardiopulmonary functions.
Detailed description
Hypothesis 1: H0: Cardiac rehabilitation has no effect on quality of life patients with CABG surgery. H1: Cardiac rehabilitation has an effect on quality of life patients with CABG surgery. Hypothesis 2: H0: Cardiac rehabilitation has no effect on sleep quality patients with CABG surgery. H1: Cardiac rehabilitation has an effect on sleep quality patients with CABG surgery. Hypothesis 3: H0: Cardiac rehabilitation has no effect on anxiety and depression patients with CABG surgery. H1: Cardiac rehabilitation has an effect on anxiety and depression with CABG surgery. H0: Cardiac rehabilitation has no effect on cardiopulmonary function patients with CABG surgery. H1: Cardiac rehabilitation has an effect on cardiopulmonary function patients with CABG surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Cardiac rehabilitation program | The experimental group patients were included in the cardiac rehabilitation program. The cardiac rehabilitation program was implemented in the cardiopulmonary rehabilitation unit with bicycle ergometry devices by a team consisting of a physical medicine and rehabilitation physician, physiotherapist and nurse. The target heart rate that could be achieved during exercise was determined according to the patient's age and the medications he/she used. The exercise intensity was planned as low and moderate according to the target heart rate percentage. The program was organized as 30 sessions, 5 days a week, for 6 weeks. The sessions were implemented for half an hour while the patients were monitored from the bicycle ergometry device. |
Timeline
- Start date
- 2025-01-01
- Primary completion
- 2025-04-29
- Completion
- 2025-04-29
- First posted
- 2025-05-14
- Last updated
- 2025-05-14
Locations
1 site across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT06970938. Inclusion in this directory is not an endorsement.