Effects of neurophysiological techniques on recovery after heart surgery
The Effect of Neurophysiological Facilitation Techniques on Pulmonary Function, Respiratory Muscle Strength and Functional Capacity in The Early Stage After Open Heart Surgery
This study tests if adding special techniques to regular rehab helps people recover better after heart surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 32 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | Dogus Universitesi Academic / other |
| Locations | 1 site (Ankara) |
| Trial ID | NCT06551714 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of neurophysiological facilitation techniques on the functional capacity and respiratory parameters of patients recovering from open heart surgery. A total of 32 patients are divided into two groups: one receiving standard phase 1 cardiac rehabilitation and the other receiving additional neurophysiological techniques. The study measures various health metrics, including vital signs, functional capacity, and pulmonary function, before and after treatment over four days. The goal is to determine if the additional techniques provide significant benefits compared to standard rehabilitation.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-75 who are undergoing their first open heart surgery and are fully cooperative.
Not a fit: Patients with certain conditions such as chronic renal failure, cognitive dysfunction, or neuromuscular diseases may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could enhance recovery outcomes for patients after open heart surgery.
How similar studies have performed: While similar rehabilitation approaches have been explored, the specific combination of neurophysiological techniques in this context is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Having open heart surgery for the first time, * Being between the ages of 18-75, * Being fully cooperative Exclusion Criteria: * Having facial, sternum and rib fractures, * Having chronic renal failure, * Development of cerebrovascular accident, * Having cognitive dysfunction, * Development of deep vein thrombosis in the post-operative period, * Having neuromuscular disease, * Having an orthopedic disability, * Intubation time longer than 24 hours, * Staying in intensive care for more than 48 hours
Where this trial is running
Ankara
- Lokman Hekim Akay Hospital — Ankara, Turkey (Türkiye) (Recruiting)
Study contacts
- Principal investigator: Yasemin Cirak, Prof. Dr. — Istinye University
- Study coordinator: Feyza merakli
- Email: feyzamrkl@gmail.com
- Phone: 05427685223
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.