NCT07311174

Brief Summary

This randomized controlled trial evaluated the effectiveness of a 10-session psychodrama intervention on reducing aggressive behavior and improving social adjustment among male adolescents with high aggression and low social adjustment in Bandar Abbas, southern Iran. Twenty-two eligible students were randomly assigned to either a psychodrama intervention group or a comparison group. Outcomes were assessed using the Buss-Perry Aggression Questionnaire and the Bell Adjustment Inventory before and after the intervention.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
22

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 5, 2023

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 7, 2023

Completed
22 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 29, 2023

Completed
2.4 years until next milestone

First Submitted

Initial submission to the registry

December 16, 2025

Completed
14 days until next milestone

First Posted

Study publicly available on registry

December 30, 2025

Completed
Last Updated

January 6, 2026

Status Verified

January 1, 2026

Enrollment Period

4 months

First QC Date

December 16, 2025

Last Update Submit

January 1, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Bell Adjustment Inventory

    Higher scores= Worst outcome (Poorer adjustment).

    Pre-intervention and immediately post-intervention (10 weeks)

  • Buss-Perry Aggression Questionnaire

    Higher scores= Worst outcome (Greater aggression).

    Pre-intervention and immediately post-intervention (10 weeks)

Study Arms (2)

Psychodrama

EXPERIMENTAL

Participants received a 10-session structured psychodrama intervention based on Blatner's protocol. Sessions were held weekly for 90 minutes.

Behavioral: Psychodrama

Standard school program

ACTIVE COMPARATOR

Participants continued with their standard school educational program. They received no additional sessions, therapy, or intervention during the 10-week study period. Other: Standard Care

Other: Control

Interventions

PsychodramaBEHAVIORAL

Participants received a 10-session structured psychodrama intervention based on Blatner's protocol. Sessions were held weekly for 90 minutes.

Psychodrama
ControlOTHER

The control group recieved no intervention during 10 weeks.

Standard school program

Eligibility Criteria

Sexmale
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Male, 7th or 8th-grade student (aged 11-13).
  • BPAQ score \> 117.
  • BAI score between 16 and 20.
  • Able to commute to after-school classes.
  • Parental informed consent obtained.

You may not qualify if:

  • Physical disability or severe illness.
  • History of major psychiatric disorders or current psychiatric medication use.
  • Unwillingness to participate or missing \>2 sessions.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kerman University of Medical Sciences

Kerman, 123456789, Iran

Location

MeSH Terms

Conditions

Aggression

Interventions

Psychodrama

Condition Hierarchy (Ancestors)

Aberrant Motor Behavior in DementiaBehavioral SymptomsBehaviorSocial Behavior

Intervention Hierarchy (Ancestors)

Mind-Body TherapiesComplementary TherapiesTherapeuticsPsychotherapy, GroupSocioenvironmental TherapyPsychotherapyBehavioral Disciplines and Activities

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
faculty member

Study Record Dates

First Submitted

December 16, 2025

First Posted

December 30, 2025

Study Start

March 5, 2023

Primary Completion

July 7, 2023

Study Completion

July 29, 2023

Last Updated

January 6, 2026

Record last verified: 2026-01

Locations