Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05489432

PREhabilitation of Candidates for REnal Transplantation

Led by University Medical Center Groningen · Updated on 2024-12-09

128

Participants Needed

1

Research Sites

140 weeks

Total Duration

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AI-Summary

What this Trial Is About

In this study a personalized, multi modal prehabilitation intervention will be offered to n = 64 patients on the kidney transplant waiting-list. The control group (n = 64) will receive care as usual. Based on a screening, comprised of questionnaires and physical test, eligible kidney transplant candidates who have modifiable problems on the domains of physical capacity, nutritional status or psychological well-being, will be randomly assigned to either the intervention or control group. The intervention will consist of a 12-week prehabilitation program followed by a 12 week consolidation program. Primary outcome will be frailty status as an indicator of overall health status and will be measured at screening (T0), 13 weeks (T1) and 26 weeks (T2)

CONDITIONS

Official Title

PREhabilitation of Candidates for REnal Transplantation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult kidney transplant candidates (≥18 years)
  • Listed for kidney transplantation on the UMCG kidney transplant waiting list at the start of the study or wait listed during the inclusion period (October 2022 - March 2025)
Not Eligible

You will not qualify if you...

  • Inability to read and/or speak Dutch
  • Combined organ transplantation (e.g., kidney+pancreas, kidney+liver)
  • For living donor kidney transplant: transplantation planned within 3 months
  • Currently involved in a lifestyle intervention program

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Medical Center Groningen

Groningen, Netherlands, 9700 RB

Actively Recruiting

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Research Team

C

Coby C Annema, PhD

CONTACT

A

Avril Haanstra, MsC

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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