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New nursing approach eases anxiety after colostomy surgery
NCT ID NCT07304544
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a 12-week nursing program based on the Roy Adaptation Model for adults who recently had a colostomy. It aimed to reduce anxiety and depression and improve quality of life compared to standard care. 115 participants were randomly assigned to either the special program or routine education, and their mental health and blood markers were measured.
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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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115 people
The number who actually took part.
- Started
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Dec 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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18 to 75 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Underwent elective colostomy (permanent or temporary) due to colorectal cancer, inflammatory bowel disease, or intestinal obstruction; * Postoperative time ≤ 1 week; * Age 18-75 years; * Consciousness clear, able to communicate normally and complete questionnaire surveys; * Voluntarily participate in the study and sign informed consent. Exclusion Criteria: * Complicated with severe cardiovascular, liver, kidney, or mental diseases; * History of anxiety, depression, or other mental disorders before surgery; * Stoma complications (e.g., stoma prolapse, ischemia, infection) requiring reoperation; * Loss to follow-up or refusal to cooperate with the study
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Genom att skicka in godkänner du våra Användarvillkor
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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West China Hospital
Chengdu, Sichuan, China
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