- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07506759
The Effect of Psychodramatic Role-Playing on Postpartum Depression, Self-Efficacy, and Perceived Social Support
The Effect of Psychodramatic Role-Playing Used in Childbirth Preparation Classes on Postpartum Depression, Self-Efficacy, and Perceived Social Support
Study Overview
Status
Intervention / Treatment
Detailed Description
Childbirth preparation education plays a crucial role in reducing anxiety, increasing maternal self-efficacy, and enhancing perceived social support during pregnancy and the postpartum period. Innovative educational approaches, such as psychodramatic role-playing, may strengthen coping skills and emotional preparedness for childbirth. This randomized controlled trial was conducted to evaluate the effectiveness of psychodramatic role-playing integrated into childbirth preparation classes provided in a maternity education program.
The study included pregnant women between 32 and 36 weeks of gestation who voluntarily participated in the childbirth education program. Participants were randomly allocated into intervention and control groups. The intervention group received structured childbirth preparation education sessions enriched with psychodramatic role-playing techniques designed to improve emotional expression, coping strategies, and social interaction. The control group received the standard childbirth preparation education program.
Data were collected at baseline and during the postpartum period using standardized measurement tools including the Edinburgh Postnatal Depression Scale (EPDS), the Multidimensional Scale of Perceived Social Support (MSPSS), and the General Self-Efficacy Scale. The primary outcomes of the study were postpartum depression, maternal self-efficacy, and perceived social support. This study aims to provide evidence on the effectiveness of psychosocial and interactive educational interventions in childbirth education programs and to support the development of evidence-based maternal care practices.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Istanbul, Turkey (Türkiye), 34668
- Zeynep Kamil Women and Children's Diseases Training and Research Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Agree to participate in the study and be able to speak and understand Turkish,
- Be 18 years of age or older,
- Be at least literate,
- Be a primiparous pregnant woman,
- Be at least 32 weeks and no more than 36 weeks pregnant,
- Have no psychological disorders or chronic illnesses.
Exclusion Criteria:
Being multiparous,
- Being less than 32 weeks pregnant,
- Being in the high-risk pregnancy category,
- Having received childbirth preparation training from another institution or individual,
- Not having completed the training program.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Psychodramatic Role-Playing Childbirth Education
Participants in the intervention group received childbirth preparation education integrated with psychodramatic role-playing techniques.
The sessions included interactive role-playing activities aimed at enhancing emotional expression, coping skills, self-efficacy, and perceived social support during pregnancy and the postpartum period.
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Psychodramatic role-playing integrated into childbirth preparation education was administered to the intervention group.
The program included structured educational sessions combined with interactive role-playing activities aimed at improving emotional expression, coping skills, maternal self-efficacy, and perceived social support during pregnancy and the postpartum period.
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Active Comparator: Standard Childbirth Education
Participants in the control group received the standard childbirth preparation education program routinely provided in the childbirth education classes without psychodramatic role-playing components.
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The control group received the standard childbirth preparation education routinely provided in childbirth education classes without psychodramatic role-playing components.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postpartum Depression
Time Frame: Postpartum week 1 and postpartum week 8
|
Edinburgh Postpartum Depression Scale will be applied to examine the effect of home visits and prenatal education on postpartum depression. Edinburgh Postpartum Depression Scale (EPDS); EPDS is a 4-point Likert style self-report scale consisting of 10 items. PRES was adapted to Turkish by Engindeniz. In Engindeniz's validity and reliability study, this scale had an internal consistency coefficient of 0.79, a split-half reliability, a cut-off of 0.80 of 12/13, a sensitivity of 0.84, a specificity of 0.88, a positive predictive value of 0.69, and a negative predictive value of 0.94. The Edinburgh Postnatal Depression Scale is a 10-item self-report scale assessing the common symptoms of depression. Each item is scored on a 4 point scale (O-3), the minimum and maximum total score ranging from O-30, respec- tively. The highest score is 30 points. If it is less than 9 points, there is no risk for depression, if it is 13 and above, there is a high risk for depression. |
Postpartum week 1 and postpartum week 8
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maternal Self-Efficacy
Time Frame: Postpartum week 1 and postpartum week 8
|
Maternal self-efficacy levels measured using the General Self-Efficacy Scale.
The General Self-Efficacy Scale was developed by Ralf Schwarzer and Matthias Jerusalem to assess individuals' general perceptions of self-efficacy in coping with stressful situations and managing challenging life events.
The scale is a self-report measure consisting of 10 items on a 4-point Likert scale (1 = not at all true, 4 = completely true).
The total score obtainable from the scale ranges from 10 to 40, with higher scores indicating a higher level of self-efficacy.
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Postpartum week 1 and postpartum week 8
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Perceived Social Support
Time Frame: Postpartum week 1 and postpartum week 8
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Perceived social support levels assessed using the Multidimensional Scale of Perceived Social Support. The Multidimensional Scale of Perceived Social Support was developed by Gregory D. Zimet and colleagues to assess the level of social support individuals perceive from their family, friends and a specific person. The scale consists of a total of 12 items and uses a 7-point Likert scale (1 = strongly disagree, 7 = strongly agree). The scale comprises three sub-dimensions: family support, friend support and support from a significant other. Each sub-dimension consists of 4 items. The total score obtained from the scale ranges from 12 to 84, with higher scores indicating a higher level of perceived social support. |
Postpartum week 1 and postpartum week 8
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Collaborators and Investigators
Sponsor
Collaborators
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Ü. Ü. Ebe Feyza KALE
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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