Clinical trial · Interventional
Mandala Painting on Perioperative Psychological Well-Being,Emotional Self-Efficacy,Anxiety
The Effect of Mandala Painting on Perioperative Psychological Well-Being, Emotional Self-Efficacy and Anxiety in Gynecologic Cancer Patients: A Randomized Controlled Study
NCT07160062CI-TRIAL-00094986completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Aim: The aim of this study was to investigate the effect of mandala painting on psychological well-being, emotional self-efficacy, and anxiety in gynecological cancer patients during the perioperative period.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Anxiety | — | UNRESOLVED | — |
| Gynecological Cancers | — | UNRESOLVED | — |
| Mandala Painting | — | UNRESOLVED | — |
| Psychological Well-being | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Mandala painting | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Intervention group
- interventionNames
- Behavioral: Mandala painting
- type
- NO_INTERVENTION
- label
- Control group
Primary outcomes (3)
- measure
- Emotional Self-Efficacy Scale
- timeFrame
- change from before implamentation patent and after 1st and 3rd days of practice
- description
- The Turkish adaptation of the scale developed by Kirk, Shutte, and Hine was conducted by Totan, İkiz, and Karaca. The scale consists of 32 items and is based on a 5-point Likert scale (1-Strongly disagree, 7-Strongly agree).
- measure
- Psychological Well-Being Scale
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
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.
References
Publications (0)
Data not yet available
No reference posted for this study.