Walking and strength training before surgery: a new strategy to boost recovery?
NCT ID NCT03954678
First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This trial tests whether starting a structured exercise program before urologic surgery can improve patients' physical fitness and reduce complications. Participants scheduled for surgery with an inpatient stay are randomly assigned to either an exercise plan (daily walking and strength training) or a nutrition plan (liquid supplements). Researchers will measure changes in mobility, strength, and body mass index, and compare the number of perioperative complications between the two groups.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A pre-surgery exercise program involving daily walking (10,000 steps) and strength training with resistance bands, compared to a nutritional supplement plan.
- What this could lead to
- If effective, this could establish a simple, low-cost way to help patients recover faster and avoid complications after major urologic surgery.
- What could go wrong
- The trial is early and the benefits of pre-surgery exercise are not yet proven. Results may vary, and not all patients may be able to follow the exercise plan.
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 400 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2019
- Expected to finish
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Jul 2028
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: * Patients scheduled for operative procedure with an inpatient postoperative stay are eligible for this study * Patients willing and able to give blood sample as part of standard of care labs * Patients willing and able to fill out questionnaire * Patients who will fill out the step log daily * Patients willing and able to sign informed consent Exclusion Criteria: * None
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Emory University Hospital
RECRUITINGAtlanta, Georgia, 30322, United States
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