Pre-Surgery workout may boost liver donor recovery
NCT ID NCT05431361
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a personalized exercise program (prehab) before living liver donation is practical and helpful. Thirty donors followed a remote exercise plan for at least 28 days before surgery. The goal was to see if a larger trial is possible, not to prove the program works.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Prehabilitation (exercise program)
- What this could lead to
- If this approach works, it could improve recovery and quality of life for living liver donors after surgery.
- What could go wrong
- This was a small, early feasibility study with only 30 participants. It was not designed to prove that prehab actually improves recovery, so results may not be conclusive.
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
-
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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30 people
The number who actually took part.
- Started
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Aug 2022
- Finished
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Dec 2024
- 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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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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: * Fluent in English for the purposes of providing informed consent, completing study-related questionnaires, and understanding intervention and other study requirements * Have a minimum of 28 days prior to scheduled LDLT Exclusion Criteria: * They plan to be absent for more than 2 weeks of the intervention period * Their health status changes during the pre-LDLT procedure which results in the loss of LLD candidacy
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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 Health Network
Toronto, Ontario, M5G 2C4, Canada
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