Effect of Home-based Training Program for Kidney Transplant Recipients (HOMETRAIN-KTR) - Trial NCT06379009
Access comprehensive clinical trial information for NCT06379009 through Pure Global AI's free database. This phase not specified trial is sponsored by Oslo University Hospital and is currently Recruiting. The study focuses on Kidney Transplant; Complications,Frailty,Physical Disability. Target enrollment is 200 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
Sponsor & Location
Oslo University Hospital
Timeline & Enrollment
N/A
Feb 07, 2024
Jan 01, 2028
Primary Outcome
6-minute walking distance test,Clinical Frailty Scale
Summary
Does home-based training work in kidney transplant recipients with reduced physical function?
 
 The goal of this clinical trial is to learn if home-based training works to better physical
 function in adult kidney transplant recipients. It will also learn about participants
 preoperative physical function. The main question it aim to answer is
 
 - Does home-based training improves physical function in kidney transplant recipients.
 
 - All the participants are assessed to have reduced physical function before the
 transplantation
 
 Participants will:
 
 - follow either a home-based training program or todays standard of physical activity
 after kidney transplantation
 
 - the program starts 4 weeks after the transplantation and lasts for 12 weeks. A
 physiotherapist will help the participants in the beginning.
 
 - the program consists of both cardio-training, strength-straining and optional activity
 
 - the training group will be followed up every week by phone. Their activity will be
 documented via patients logs and heart rate monitor.
 
 - the effect of the training will be evaluated one year after the transplantation
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06379009
Non-Device Trial