Assessing exercise capacity in kidney transplant recipients
Determinants of Exercise Capacity in Kidney Transplant Recipients
This study looks at how far kidney transplant patients can walk in six minutes to see what affects their exercise ability and help them with their recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 27 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Hacettepe University Academic / other |
| Locations | 1 site (Ankara) |
| Trial ID | NCT06706154 on ClinicalTrials.gov |
What this trial studies
This observational study aims to evaluate the factors influencing the distance covered in a 6-minute walk test among kidney transplant recipients. It focuses on patients who are at least six months post-transplant and have not engaged in regular exercise. By analyzing the determinants of exercise capacity, the study seeks to provide insights into the physical rehabilitation needs of this population.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-65 who have undergone kidney transplantation at least six months prior and do not have regular exercise habits.
Not a fit: Patients with musculoskeletal problems, neurological impairments, chronic lung diseases, or recent cardiovascular events may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could help improve exercise programs and rehabilitation strategies for kidney transplant recipients.
How similar studies have performed: While there may be limited studies specifically targeting exercise capacity in kidney transplant recipients, similar approaches in other transplant populations have shown promising results.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with kidney transplantation * At least 6 months after the kidney transplant * Being aged 18-65 * Not having regular exercise habits * Voluntary participation in the study Exclusion Criteria: * Having a musculoskeletal problem that may interfere with the tests * Having neurological impairment * Having chronic lung disease * Having had any cardiovascular event in the last 6 months
Where this trial is running
Ankara
- Hacettepe University — Ankara, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Merve Firat
- Email: mervefirat@ahievran.edu.tr
- Phone: +90 850 441 02 44
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.