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CompletedNCT07372469PD-NURSUpdated Jul 28, 2026

Psychodrama for Mental Health Promotion in Nursing Students

An interventional study of Psychodrama Group and Presentation Group in Mental Health Promotion, sponsored by Marmara University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-28.

Sponsored by Marmara University · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 10 months after the study started (first participant enrolled Mar 2024, registered Jan 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Mental Health Promotion

Keywords

  • Psychodrama
  • Nursing students
  • Mental health
  • Psychosocial intervention
03

In context

Psychological Well-Being

971 studies on the registry are indexed under Psychological Well-Being; 502 are open to participants now.

This study's enrollment of 60 is below the median of 116 across 830 interventional studies indexed under Psychological Well-Being.

Browse Psychological Well-Being studies →

Lead sponsor

Marmara University is the lead sponsor of 576 studies on the registry; 136 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • Being under 18 years of age
  • Not being a nursing student
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    Psychodrama Group

    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.

    Behavioral: Psychodrama Group

  • Active comparator
    Presentation Group

    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.

    Behavioral: Presentation Group

Interventions

  • BehavioralPsychodrama Group

    A psychodrama-based group intervention delivered in weekly sessions, using experiential techniques such as role-playing and guided enactments to support mental health promotion.

  • BehavioralPresentation Group

    Participants received a group-based educational intervention delivered once weekly for 12 weeks. Students prepared group presentations based on themes related to mental health promotion, which were presented in a classroom setting and followed by moderated group discussions. Psychodrama techniques, role-playing, or dramatic enactments were not used.

06

What researchers measure

Primary outcomes

  1. Mental Health Promotion Scale Total Score

    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.

    Time frame: Baseline and immediately after the 12-week intervention

Secondary outcomes

  1. Change in Mental Health Promotion Scale Subdimension Scores

    The secondary outcomes were the scores of the 12 subdimensions of the Mental Health Promotion Scale: Friendship (score range: 5-25), Values (4-20), Personal Development (6-30), Sexuality (4-20), Self-Respect (4-20), Coping with Stress (3-15), Physical Health (3-15), Family and Close Relationships (3-15), Communication (6-30), Saying-No Skills (3-15), Anger Control (3-15), and Self-Recognition (3-15). Higher scores indicate greater ability in the corresponding mental health promotion domain. Changes were evaluated by comparing baseline and post-intervention subdimension scores.

    Time frame: Change from baseline to immediately after the 12-week intervention

07

Study locations

1 site
  • Istanbul Kent University
    Istanbul, Kağıthane 34406, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: Yes — De-identified individual participant data underlying the results reported in the article may be shared upon reasonable request.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 28, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07372469
Lead sponsor
Marmara University
Responsible party
ÖZGE KARACA (Research Assistant, Marmara University) — Principal investigator
First posted
Jan 28, 2026
Start date
Mar 1, 2024
Primary completion
May 31, 2024
Completion
May 31, 2024
Last update
Jul 28, 2026

Study contacts

Çağlar Şimşek, PhD
principal investigator · Marmara University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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