Home-based training program for kidney transplant recipients
Evaluating the Effect of a Structured Home-based Physical Training Program for Kidney Transplant Recipients With Impaired Pre-transplant Physical Function
This study tests whether a home-based training program can help kidney transplant recipients improve their physical strength and function after their surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Oslo University Hospital Academic / other |
| Locations | 1 site (Oslo) |
| Trial ID | NCT06379009 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of a structured home-based training program aimed at improving physical function in adult kidney transplant recipients who have reduced physical function prior to transplantation. Participants will be randomly assigned to either the training program or standard physical activity care, starting four weeks post-transplant and lasting for 12 weeks. The program includes cardio and strength training, with weekly follow-ups by a physiotherapist to monitor progress. The study aims to assess the impact of this intervention on physical function and frailty one year after transplantation.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older undergoing kidney transplantation with low pre-transplant physical function.
Not a fit: Patients who do not have reduced physical function prior to transplantation may not benefit from this intervention.
Why it matters
Potential benefit: If successful, this program could significantly enhance the physical recovery and overall quality of life for kidney transplant recipients.
How similar studies have performed: Previous studies have shown promising results for exercise interventions in similar populations, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Being 18 years old or older and going through Ktx * Scores 75 or lower at physical function at SF-36 at time of KTx * Able to perform the 6MWT * Able to speak, read and understand Norwegian or English * Being mentally and cognitively capable of participating in the intervention and responding to follow-up questionnaires Exclusion Criteria: \- none
Where this trial is running
Oslo
- Oslo University Hospital — Oslo, Norway (Recruiting)
Study contacts
- Principal investigator: Marit Helen Andersen — Oslo University Hospital
- Study coordinator: Tommy Aronsen, MD
- Email: tomaro@ous-hf.no
- Phone: 004790923913
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.