Home workouts could protect kidney transplant Patients' hearts
NCT ID NCT04123951
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a 12-week home-based exercise program can improve heart health in kidney transplant recipients. Half of the 50 participants will follow the exercise plan, while the other half continues usual care. Researchers will use detailed MRI scans to measure changes in heart structure and function.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- home-based exercise program
- What this could lead to
- If it works, this could point toward a simple, low-cost way to reduce heart disease risk in kidney transplant recipients.
- What could go wrong
- This is a small pilot study with only 50 participants, so results may not apply to everyone. The exercise program is short (12 weeks) and may not produce lasting heart benefits.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2020
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age great than 18 years old * Prevalent RTR longer than 1year * Able and willing to give informed consent * Increased cardiometabolic risk, with at least one of: Diabetes mellitus Dyslipidaemia Hypertension History of ischaemic heart disease or cerebrovascular disease Obesity (BMI above 30) Exclusion Criteria: * Unable to undertake exercise due to physical or psychological barriers * Unable to undergo CMR scanning (incompatible implants, claustrophobia, allergy to agents) * Contraindication to exercise training (American College of Sports Medicine guidelines) * Female participants who are pregnant, lactating, or planning pregnancy during the course of the study. * Scheduled elective surgery or other procedures requiring general anaesthesia during the study. * Any other significant disease or disorder (i.e. significant co-morbidity including unstable hypertension, potentially lethal arrhythmia, myocardial infarction within 6 months, unstable angina, active liver disease, uncontrolled diabetes mellitus (HbA1c greater than or equal to 9%), advanced cerebral or peripheral vascular disease) which, in the opinion of the patient's own clinician the Principle Investigator may either put the participants at risk because of participation in the study, or may influence the result of the study, or the participant's ability to participate in the study. * Inability to give informed consent or comply with testing and training protocol for any reason.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University Hospital Leicester NHS Trust
Leicester, Leicestershire, LE5 4PW, United Kingdom
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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