Coloring away cancer anxiety: mandala painting tested in surgery patients
NCT ID NCT07160062
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study looked at whether mandala painting can improve psychological well-being, emotional self-efficacy, and reduce anxiety in women with gynecologic cancer during the perioperative period. 84 patients were randomly assigned to either a mandala painting session or standard care. The painting sessions lasted 35-50 minutes, and researchers measured changes in anxiety and well-being using standard questionnaires.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- mandala painting
- What this could lead to
- If effective, mandala painting could offer a simple, drug-free way to ease anxiety and boost emotional well-being for women undergoing gynecologic cancer surgery.
- What could go wrong
- This is a small, completed study with 84 participants, so results may not apply to everyone. The intervention is behavioral, so benefits may be modest or not reproducible in larger groups.
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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84 people
The number who actually took part.
- Started
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May 2025
- Finished
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Aug 2025
- 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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Female participants only
- 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:- * 18 years of age or older, * Diagnosed with any type or stage of gynecological cancer, * In the perioperative period and scheduled for surgery, * Willing to participate in this intervention, * With written consent, * Volunteering to participate in the study Exclusion Criteria: * Those with a serious physical or mental illness, * Those with intellectual or cognitive impairment, * Those with serious perioperative medical complications, * Those who withdrew or dropped out of the study early, * Those who were not willing to participate in the study.
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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.
Contacts and locations
Locations
-
Eskişehir Osmangazi University
Eskişehir, Turkey (Türkiye)
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