Could a resilience program ease the emotional toll of stoma surgery?
NCT ID NCT07787637
First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time
Summary
This study looks at how having a new stoma (an opening in the body for waste to leave) affects both patients and their partners, and whether resiliency training can improve their quality of life. Researchers will measure quality of life and psychological resilience in patients undergoing their first stoma creation. The goal is to see if this training offers meaningful support during a challenging adjustment period.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- resiliency training
- What this could lead to
- If effective, resiliency training could become a standard support tool to help new stoma patients and their partners adapt and maintain a better quality of life.
- What could go wrong
- This is a small, early-stage study, so results may not apply broadly. The training's benefits are uncertain, and it may not significantly improve quality of life for all participants.
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
-
About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2025
- Expected to finish
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Jan 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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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: patient who will be undergoing new stoma creation \- Exclusion Criteria: * history of previous stoma
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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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Northwestern Memorial Hospital
Chicago, Illinois, 60011, United States
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