- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07305571
The Effect of Psychodrama-Based Group Work
The Effect of Psychodrama-Based Group Work on Postpartum Women's Depression and Forgiveness Tendencies: A Randomised Controlled Study
Aims This study examined the effect of psychodrama-based group work on postpartum women's tendencies toward depression and forgiveness.
Methods This study used a pretest-posttest-follow-up randomised controlled experimental method. The study sample consisted of 23 postpartum mothers (11 experimental and 12 control) whose babies were receiving treatment in the neonatal intensive care unit between April and June 2025. While psychodrama-based group intervention was applied to the experimental group, no intervention was performed in the control group. Data were collected using a personal information form, Postnatal Depression Screening Scale, and Forgiveness Scale.
Results In the study, it was found that the mean forgiveness scores in the final test and follow-up measurements of the postpartum women in the experimental group were statistically significantly higher compared to the control group (p<0.05). In the final test and follow-up measurements, the mean postpartum depression scores of the women in the experimental group were found to be statistically significantly lower than those of the mothers in the control group (p<0.05).
Conclusions Psychodrama-based group work increased forgiveness tendencies and reduced depression levels in postpartum women. In this regard, it is recommended that psychodrama sessions be conducted for postpartum women.
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Bergama
-
Izmir, Bergama, Turkey (Türkiye), 35700
- Bergama Necla Mithat Öztüre State Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age between 18-55 years or (until menopause)
- Having the mental capacity and sufficient communication skills to follow the research instructions, being literate.
- Having an infant receiving treatment in the neonatal intensive care unit.
Exclusion Criteria:
- Having a condition that impairs communication
- Having a diagnosed mental illness.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: psychodrama-based group intervention
Participants will receive an 8-session psychodrama-based group intervention.
|
For postpartum mothers in the experimental group, a psychodrama-based group intervention was carried out face-to-face, with one session per week, each lasting 120 minutes, for a total of 8 sessions (over 8 weeks).
no intervention was performed in the control group
|
|
No Intervention: Control
Throughout the study, the psychodrama-based group intervention was applied only to the experimental group, and no intervention was performed in the control group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postpartum Depression Screening Scale
Time Frame: Baseline (pretest), 8 weeks (posttest) and one month after the posttest
|
Evaluation of the change in the total score of the Postpartum Depression Screening Scale.
The minimum score obtained from the scale was 35, and the maximum score was 175.
Higher scores indicate higher levels of postpartum depression.
|
Baseline (pretest), 8 weeks (posttest) and one month after the posttest
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Forgiveness Scale
Time Frame: Baseline (pretest), 8 weeks (posttest) and one month after the posttest
|
Forgiveness Scale, developed by Ersanlı and Batık, designed to measure individuals' levels of self-forgiveness and forgiveness of others.
The scale is scored from "strongly disagree" to "strongly agree," with higher scores indicating higher levels of forgiveness.
|
Baseline (pretest), 8 weeks (posttest) and one month after the posttest
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Merve Şahin, PhD, RN, Bergama Necla Mithat Öztüre State Hospital
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 (Estimated)
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
- MERVE-RCT-2025-PAD
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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