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CompletedNCT07094243Updated Jul 31, 2025

Motivational Psychotherapy for Adolescent Depression

An interventional study of Motivational Psychotherapy in Depression and Low Academic Self-Concept, sponsored by Atefe Momeni. Completed at 1 site in Iran. Open to female participants aged 13 Years to 17 Years. Per ClinicalTrials.gov, last updated 2025-07-31.

Sponsored by Atefe Momeni · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 8 months after the study started (first participant enrolled Nov 2023, registered Jul 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Non-randomized
Ages
13 Years to 17 Years
Sex
Female
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Study summary

This pilot study investigates the effectiveness of Motivational Psychotherapy in reducing symptoms of depression and improving academic self-concept among adolescent girls in Iran. A total of 30 participants aged 13 to 17 were randomly assigned to an experimental group receiving Motivational Psychotherapy and a control group receiving no treatment. The intervention consisted of 8 weekly sessions based on the principles of motivational interviewing and was tailored to adolescent needs. Outcomes were measured using the Beck Depression Inventory-II (BDI-II) and the Academic Self-Concept Questionnaire (ASCQ). Results suggest the potential benefit of this culturally sensitive approach in non-Western adolescent populations.

Read the detailed description

This randomized controlled pilot trial evaluated the effectiveness of Motivational Psychotherapy in reducing depressive symptoms and improving academic self-concept among adolescent girls in Iran. A total of 30 participants aged 13-17 years were randomly assigned to either the Motivational Psychotherapy group or a no-intervention control group.

The intervention consisted of 8 weekly individual sessions (60 minutes each) based on a manualized Motivational Psychotherapy protocol, adapted for adolescents in a non-Western context. The sessions focused on resolving ambivalence, enhancing intrinsic motivation, and strengthening environmental support.

Outcome measures included the Beck Depression Inventory-II (BDI-II) for depressive symptoms and the Academic Self-Concept Questionnaire (ASCQ) for academic self-concept. Data were analyzed using ANCOVA to control for baseline differences between groups. The results showed significant improvement in depression scores and academic self-concept in the intervention group compared to the control group, supporting the feasibility and cultural relevance of Motivational Psychotherapy for adolescent mental health.

02

Conditions studied

  • Depression
  • Low Academic Self-Concept

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Keywords

  • Adolescent mental health
  • Motivational psychotherapy
  • Motivational interviewing
  • Academic self-concept
  • Pilot trial
  • Non-Western context
03

In context

Depression

8,057 studies on the registry are indexed under Depression; 1,641 are open to participants now.

This study's enrollment of 30 is below the median of 84 across 6,720 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

This is the only study on the registry with Atefe Momeni as lead sponsor.

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

04

Who can participate

Ages eligible
13 Years to 17 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:

  • Inclusion Criteria:
  • Female adolescents aged 13 to 17 years
  • Clinical diagnosis of mild to moderate depression based on DSM-5 criteria
  • Currently enrolled in middle or high school
  • Informed consent obtained from parents/legal guardians and assent from adolescents

Exclusion Criteria:

  • Severe depression requiring urgent psychiatric care
  • Diagnosis of a major psychiatric disorder (e.g., bipolar disorder, psychosis)
  • Ongoing psychotherapy or psychotropic medication use
  • Significant cognitive or developmental disability interfering with participation

Exclusion Criteria:

-

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Motivational Psychotherapy

    Participants receive Motivational Psychotherapy intervention.

    Behavioral: Motivational Psychotherapy

  • No intervention
    No Intervention

    Participants receive no psychological intervention during the study period.

Interventions

  • BehavioralMotivational Psychotherapy

    A structured short-term intervention based on motivational psychotherapy, delivered in individual sessions over 8 weeks to improve adolescent depression and academic self-concept.

06

What researchers measure

Primary outcomes

  1. Change in Depression Score from Baseline to 8 Weeks Post-Intervention

    Depression symptoms will be assessed using the Beck Depression Inventory-II (BDI-II; range 0-63, higher scores indicate worse depression). The mean change in BDI-II scores from baseline to 8 weeks will be analyzed between the Motivational Psychotherapy and control groups.

    Time frame: Baseline and 8 weeks after start of intervention

Secondary outcomes

  1. Change in Depression Score from Baseline to 8 Weeks Post-Intervention

    Depression symptoms will be assessed using the Beck Depression Inventory-II (BDI-II). The primary outcome is the mean change in BDI-II scores from baseline to 8 weeks after the intervention. The comparison will be made between the experimental group (receiving motivational psychotherapy) and the control group.

    Time frame: Baseline and 8 weeks after start of intervention

07

Study locations

1 site
  • Islamic Azad University, Tehran Electronic Branch
    Tehran, Tehran Province 14398-14994, Iran
08

References and documents

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 31, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07094243
Lead sponsor
Atefe Momeni
Responsible party
Atefe Momeni (Clinical Psychology Researcher, Islamic Azad University, Tehran Electronic Branch, Islamic Azad University, Sanandaj) — Sponsor-investigator
First posted
Jul 30, 2025
Start date
Nov 5, 2023
Primary completion
Jan 20, 2024
Completion
Jan 20, 2024
Last update
Jul 31, 2025

Study contacts

Hossein Sahebdel, Associate Professor of Counsel
principal investigator · Islamic Azad University, Tehran Electronic Branch

Oversight

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

Not currently enrolling

This study is completed, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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