- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07416071
Mandala Therapy in Nurses: Effects on Psychological Well-Being and Organizational Cynicism
Evaluation of the Effect of Mandala Therapy on Nurses' Psychological Well-Being and Organizational Cynicism Level
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Nursing is a profession characterized by high emotional labor, intensive workload, and continuous occupational stress, which may negatively affect psychological well-being and contribute to negative organizational attitudes such as organizational cynicism. Supporting nurses' psychological well-being is therefore essential for sustaining professional functioning and quality of care.
Mandala therapy is an art-based behavioral intervention that provides individuals with a space for free expression through unstructured drawing and coloring activities. Unstructured mandala practices allow participants to express their inner experiences without predetermined guidance, supporting emotional awareness and self-regulation.
This experimental study was conducted to evaluate the effect of unstructured mandala therapy on nurses' psychological well-being and organizational cynicism levels. The study was carried out with nurses working in a public training and research hospital. Participants were allocated to an intervention group receiving unstructured mandala therapy and a control group receiving routine working conditions.
Mandala therapy sessions were conducted in small groups over a defined period, based on a free-expression approach. Psychological well-being and organizational cynicism levels were assessed at baseline and after the intervention using standardized and validated measurement tools. Ethical approval was obtained prior to data collection, and written informed consent was obtained from all participants. The study was retrospectively registered.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Rize, Turkey (Türkiye)
- Public Training and Research Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Having at least 6 months of professional nursing experience at the hospital where the study is conducted
- Willingness to participate voluntarily in the study
Exclusion Criteria:
- Being on leave or on medical report during the data collection period
- Participation in individual psychotherapy or group-based intervention programs
- Receiving psychiatric medication treatment
- Having visual impairments or visual disorders
- Having prior experience with meditation practices
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mandala
Participants receiving unstructured mandala therapy sessions.
|
Unstructured mandala drawing and coloring activities were conducted as a behavioral intervention, allowing participants to freely express their emotions without predefined guidelines or themes.
|
|
No Intervention: Control
Participants continuing routine working conditions without any intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Psychological Well-Being
Time Frame: Baseline, 4 weeks after intervention initiation, and 8 weeks post-intervention
|
Psychological well-being will be assessed using the Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS), a validated 14-item scale ranging from 14 to 70, with higher scores indicating better psychological well-being.
|
Baseline, 4 weeks after intervention initiation, and 8 weeks post-intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Organizational Cynicism
Time Frame: Baseline, 4 weeks after intervention initiation, and 8 weeks after intervention initiation
|
Organizational cynicism was assessed using the Organizational Cynicism Scale, a 13-item instrument rated on a 5-point Likert scale (1 = strongly disagree to 5 = strongly agree).
Total scores range from 13 to 65, with higher scores indicating higher levels of organizational cynicism.
|
Baseline, 4 weeks after intervention initiation, and 8 weeks after intervention initiation
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stress Level
Time Frame: Baseline, 4 weeks after intervention initiation, and 8 weeks after intervention initiation
|
Stress level was assessed using a self-reported numerical rating scale (NRS) ranging from 1 (no stress) to 10 (maximum stress).
Higher scores indicate higher perceived stress levels.
|
Baseline, 4 weeks after intervention initiation, and 8 weeks after intervention initiation
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Sarı Öztürk E, Kılıçarslan Törüner E. Effects of mandala-based interventions on psychological outcomes in nurses. Journal of Nursing Management. 2023.Wang TQ. Mandala therapy: What it is and what it offers. The Asian Educational Therapist. 2024;2(2):13-22.
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023/135
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Study Data/Documents
-
No individual participant data or supporting information are available for sharing.
Information identifier: 2023/135Information comments: No additional comments.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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