Transplantoux Health Evaluation Study

NCT02533245 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 500

Last updated 2024-07-12

No results posted yet for this study

Summary

The primary aim is to evaluate the short- and long-term effect of the 'Transplantoux' exercise training intervention in solid organ transplant recipients with matched control sample of transplant recipients in view of selected Patient Reported Outcomes (PRO), i.e. health-related quality-of-life (HRQOL), psychosocial and behavioral variables, using a quasi-experimental design.

Conditions

  • Quality of Life

Interventions

OTHER

Home-based indiviualized exercise training program

Based on these results of the cardiopulmonary exercise test (CPET) on a cycle ergometer, an individualized training program (cycling/hiking) is prescribed by a physical therapist for 6 months (3x/week, ≥30min/session).

OTHER

Supervised group training sessions

7 supervised group training sessions (cycling/hiking) are organized by a physiotherapist

OTHER

Climb of the Mont Ventoux

Cycle or hike up the Mont Ventoux (25.7 km, average slope 4.5%)

Sponsors & Collaborators

  • University of Basel

    collaborator OTHER
  • Universitaire Ziekenhuizen KU Leuven

    lead OTHER

Principal Investigators

  • Diethard Monbaliu, MD, PhD · University Hospital Leuven, Abdominal Transplant Surgery

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2025-01-31
Completion
2025-01-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02533245 on ClinicalTrials.gov