Health optimization before kidney tumor surgery
Prehabilitation Prior to Surgery for Kidney Tumors: A Randomized Controlled Research Study (Pre-KiT)
This study tests whether a month-long health program before kidney tumor surgery can help people recover better and feel more satisfied after their operation compared to standard care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 65 Years and up |
| Sex | All |
| Sponsor | Herlev and Gentofte Hospital Academic / other |
| Locations | 1 site (Herlev) |
| Trial ID | NCT06745609 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of a one-month prehabilitation program prior to surgery for kidney tumors. The prehabilitation process includes a comprehensive health assessment, assisted smoking cessation, and a home exercise program. Participants will be divided into an intervention group receiving prehabilitation and a control group receiving standard care. The study will assess recovery satisfaction and maintenance of physical abilities post-surgery between the two groups.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 65 and older with a cT1 kidney tumor scheduled for partial or radical nephrectomy.
Not a fit: Patients who are not eligible for a postponement of surgery or do not understand Danish or English may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to faster recovery and improved quality of life for patients undergoing surgery for kidney tumors.
How similar studies have performed: Other studies have shown promising results with prehabilitation approaches in surgical recovery, indicating potential for success in this trial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 65 years or older * cT1 kidney tumor, scheduled for either partial or radical nephrectomy. * Clinical Frailty Scale 3-6 Exclusion Criteria: * It is determined by an attending physician, or at a multi-disciplinary team-conference, that a 2-4 week postponement of surgery will not be beneficial for the participant. * Participant does not understand Danish og English
Where this trial is running
Herlev
- Department of Urology, Herlev and Gentofte Hospital — Herlev, Denmark (Recruiting)
Study contacts
- Study coordinator: Marie M Haslund, MD
- Email: marie.mykloey.haslund@regionh.dk
- Phone: 004538682699
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.