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NCT Number: NCT06379009

Effect of Home-based Training Program for Kidney Transplant Recipients (HOMETRAIN-KTR)

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

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Oslo University Hospital

Oslo, 0372, Norway

Location status: Recruiting

About this study

Title:

Evaluating the effect of a structured home-based physical training program for kidney transplant recipients with impaired pre-transplant physical function (HOMETRAIN KTR)

Background and Aims:

Frailty and impaired physical function are prevalent among patients undergoing kidney transplantation (KTx), and is an independent risk factor for poor outcome after transplantation. Limited number of studies have prospectively investigated the efficacy of exercise training for KTx-recipients with low pre-transplant physical function. Our aim is to evaluate the effect of a structured 12 week home-based physical training program delivered to recipients with low pre transplant physical function, on physical function and frailty at 1-year post transplant.

Method:

HOMETRAIN-KTR is a 2-arm unblinded Norwegian clinical trial with RCT design. Patients will be recruited at admission for KTx at Oslo University Hospital, Rikshospitalet. Patients who score below 60 at 36-Item Short Form Survey will be included and tested with 6-minute walking test, Clinical Frailty Scale, hand-grip strength, 30 seconds Sit-to-Stand test, and questionnaire about physical activity and psychological distress. Included patients are randomized to either training group or control group (standard of care). The training group will, under supervision by a physiotherapist, start a 12-week structured home-based training program from week 4 post-KTx. The training program consist of a combination of strength training, cardio training and optional activities. During the intervention period, the intervention group will receive regular follow-up by phone. The training sessions will be documented via patients logs and heart rate monitor. At one year post-KTx, all patients will undergo the same tests as at inclusion.

Inclusion of patients will start in January 2024, and continue for the next 2-3 years. The investigators aim to include 200 patients, 100 in each arm. The study will evaluate physical function, frailty, graft function, patient survival, HRQoL and physiological distress during the time-span of the study.

Hypothesis:

The HOMETRAIN-KTR study is supposed to bring new knowledge about the effect of a physical training program on frail KTx-recipients. Such information is highly relevant to improve KTx outcomes and to optimize the utilization of the limited source of donor organs.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Training

Other

12 week home-based training program

Primary outcomes

  1. 6-minute walking distance test

    Time frame: Baseline and after 52 weeks

    Test of physical function. How many meters the patient manage to walk in 6 minutes.

  2. Clinical Frailty Scale

    Time frame: Baseline and after 52 weeks

    Test for frailty. Validated test for this purpose. Score 1-9. The higher the score the more frail

Secondary outcomes

  1. Hand-grip strength

    Time frame: Baseline, week 7, week 26 and week 52

    Using a hand-dynamometer to measure hand-grip strength. Average of 3 trials

  2. 30 seconds Sit-to-stand test

    Time frame: Baseline, week 7, week 26 and week 52

    Get up from chair. Number of repetitions in 30 seconds

  3. Bone density test

    Time frame: Week 7 and week 52

    Dual-energy X-ray absorptiometry (DXA)

  4. Bioelectrical impedance phase angle to measure muscle mass and strength.

    Time frame: Week 7 and 52

    Measuring bioelectrical impedance phase angle with a machine called BWA 2,0 Body. Water Analyzer. Phase angle is an indicator of muscular death, and is inversely related to muscle mass and strength in frail subjects.

Study contacts

Contact information is provided by the study sponsor or research team.

Krstian Heldal, MD, PHD

CONTACT

[email protected]

004790018417

Tommy Aronsen, MD

CONTACT

[email protected]

004790923913

Sponsors and collaborators

Lead sponsor

Oslo University Hospital

Other

Collaborators

  • South-Eastern Norway Regional Health Authority

Registry information

Official study title

Evaluating the Effect of a Structured Home-based Physical Training Program for Kidney Transplant Recipients With Impaired Pre-transplant Physical Function

Important dates

Study start
2024
Primary completion
2027
Study completion
2028
First posted
Apr 23, 2024
Registry last updated
Apr 24, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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