Walking and mental imagery may tame Post-Cancer bowel troubles
NCT ID NCT07732894
First seen Jul 29, 2026 · Last updated Jul 30, 2026 · Updated 1 time
Summary
This trial tests whether adding aerobic exercise and guided imagery to standard care can reduce bowel symptoms and improve quality of life in people with low anterior resection syndrome (LARS) after rectal cancer surgery. Participants will be randomly assigned to either the exercise-plus-imagery group or standard care alone. The study measures changes in bowel function, physical capacity, and well-being over the intervention period.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- aerobic exercise and guided imagery
- What this could lead to
- If it works, this could offer a simple, drug-free way to manage bowel symptoms and improve quality of life for rectal cancer survivors.
- What could go wrong
- This is a small, early-stage trial with only 50 participants. The benefits seen may not apply to all patients, and the exercise and imagery routines require ongoing commitment.
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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Dec 2025
- Expected to finish
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May 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 to 65 years
- 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: * Upper-Middle-Lower Rectal Cancer * Having undergone surgery with TMJ * Having a protective ileostomy and a closed stoma * Being tumor-free according to laboratory reports (carcinoembryonic antigen), endoscopic findings, and abdominal ultrasonography and/or computed tomography data * Having at least minor LARS scores ("between 21" and "42") according to the -LARS scoring questionnaire * Having the ability to perform voluntary perineal traction contractions with perineal palpation * Being a volunteer with informed consent Exclusion Criteria: * History of incontinence or defecation disorder not related to rectal cancer * Having another type of surgery for rectal cancer (Hartmann procedure, abdominoperineal excision, transanal endoscopic microsurgical resection, or sigmoid resection) * Deterioration in general health, neurological disease and/or physical disability * BMI \> 30 kg/m2 (obese individuals) * Inability to answer questions or make interventions due to mental disorder
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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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Memorial Bahçelievler Hospital
RECRUITINGIstanbul, Turkey (Türkiye)
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