Home-based Exercise and Physical Activity Intervention After Kidney Transplantation: Impact of Exercise Intensity
Launched by KU LEUVEN · Feb 7, 2024
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how different levels of exercise can help people who have recently received a kidney transplant. The goal is to see if a home-based exercise program can improve physical fitness, heart health, gut health, and overall quality of life for these patients. Participants will be divided into three groups: one will do gentle exercises like stretching, another will engage in moderate-intensity workouts like aerobic exercises and strength training, and the third group will participate in more intense workouts. The study will also look at how well these exercises can be maintained after the initial training period.
To be eligible for this trial, participants must be adults who have recently received a kidney transplant and are generally healthy enough to exercise. However, those with serious heart issues, uncontrolled diabetes, or severe lung problems, among other criteria, will not be included. If you join the trial, you can expect to follow an exercise plan for six months with support and guidance, and you’ll be helping researchers understand the best ways to keep kidney transplant recipients active and healthy.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • De novo adult KTRs
- Exclusion Criteria:
- • Underlying heart disease, defined as aberrant CPET, unstable angina, non-revascularized lesions or life-threatening arrhythmias
- • Uncontrolled hypertension
- • Uncontrolled diabetes, defined as HbA1c ≥ 9%
- • Musculoskeletal disorders not allowing physical training on a cycle ergometer, or any other medical reasons by the physician considered to be a contraindication for moderate or high-intensity physical exercise
- • Multi-organ transplantation
- • Ongoing treatment for malignancies
- • Unable to understand Dutch
- • No access to smartphone and/or computer with internet access
- • Severe pulmonary disease defined as either forced vital capacity (FVC) \<50%, one-second value (FEV1) \<50%, or a diffusing capacity for carbon monoxide (DLCO) \<40% that excludes all serious underlying respiratory disease (pulmonary fibrosis, COPD GOLD II-IV, PAH).
About Ku Leuven
KU Leuven, a prestigious research university located in Belgium, is renowned for its commitment to advancing medical science and improving patient care through innovative clinical trials. With a strong emphasis on interdisciplinary collaboration, KU Leuven integrates cutting-edge research with clinical practice, facilitating the development of new therapeutic strategies and medical technologies. The institution's robust infrastructure and expertise in various fields, including biotechnology, pharmacology, and public health, position it as a leader in conducting high-quality clinical research that adheres to rigorous ethical standards and regulatory requirements. Through its clinical trials, KU Leuven aims to contribute significantly to the global biomedical landscape and enhance health outcomes for diverse populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Leuven, , Belgium
Ghent, , Belgium
Patients applied
Trial Officials
Amaryllis Van Craenenbroeck, MD, PhD
Principal Investigator
KU Leuven
Patrick Calders, PhD
Principal Investigator
University Ghent
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported