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临床试验/NCT07372469
NCT07372469已完成不适用

The Effect of Psychodrama on Mental Health Promotion in Nursing Students: A Randomized Controlled Trial

Marmara University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年3月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
Mental Health Promotion Level

研究概览

简要总结

This randomized controlled trial aimed to examine the effect of a psychodrama group intervention on mental health promotion among nursing students. Participants were randomly assigned to an intervention group or a control group. The intervention group received weekly psychodrama sessions for 12 weeks, while the control group prepared group presentations on the same themes without psychodrama techniques. Mental health promotion levels were assessed before and after the intervention using a validated scale.

详细描述

This study was designed as a randomized controlled trial conducted among nursing students. Participants were randomly assigned to either an intervention group or a control group. The intervention group participated in a psychodrama group intervention consisting of 12 weekly sessions, each lasting approximately 120-150 minutes. Sessions were facilitated by a trained psychodramatist and followed the classical psychodrama structure, including warm-up, action, and sharing phases.

The control group participated in weekly group presentations and discussions on the same themes as the intervention group but did not receive any psychodrama techniques. Mental health promotion levels were assessed before and after the intervention using the validated Mental Health Promotion Scale.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Outcomes Assessor)

盲法说明

Due to the nature of the intervention, participants and intervention providers could not be blinded. Group allocation was masked in the coded dataset, and statistical analyses were conducted by an independent researcher who was blinded to group allocation.

入排标准

年龄范围
18 Years 至 45 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Being a nursing student
  • Aged 18 years or older
  • Voluntary participation in the study

排除标准

  • Being under 18 years of age
  • Not being a nursing student

研究组 & 干预措施

Presentation Group

Active Comparator

Participants in this group participated in weekly group sessions conducted concurrently with the intervention group for 12 weeks. Students prepared and delivered group presentations on topics aligned with the themes addressed in the psychodrama sessions. Presentations were shared in a classroom setting and followed by moderated group discussions. No psychodrama techniques, role-playing, or dramatic enactments were used.

干预措施: Presentation Group (Behavioral)

Psychodrama Group

Experimental

Participants in this group received a structured psychodrama-based group intervention conducted once weekly for 12 weeks. The program was organized around thematic sessions including communication skills, self-awareness, self-esteem, personal development, values, family and close relationships, peer relationships, stress coping, anger management, assertiveness, sexuality, and physical well-being. Sessions involved experiential psychodramatic techniques such as role-playing, group games, and guided enactments aimed at enhancing emotional expression, interpersonal awareness, coping skills, and mental health promotion.

干预措施: Psychodrama Group (Behavioral)

结局指标

主要结局

Mental Health Promotion Level

时间窗: Baseline and immediately after the 12-week intervention

Mental health promotion levels were assessed before and after the intervention using the Mental Health Promotion Scale, a validated self-report instrument.

Mental Health Promotion Scale Total Score

时间窗: Baseline and immediately after the 12-week intervention

The Mental Health Promotion Scale is a 47-item self-report measure rated on a 5-point Likert scale. Total scores range from 47 to 235, with higher scores indicating greater mental health promotion ability.

次要结局

  • Change in Mental Health Promotion Scale Subdimension Scores(Change from baseline to immediately after the 12-week intervention)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

ÖZGE KARACA

Research Assistant

Marmara University

研究点 (1)

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