NCT06619821

Brief Summary

The study aims to examine the effectiveness of joint parent-adolescent intervention in improving the mental health outcomes of participants, specifically by reducing symptoms of depression, anxiety, and PTSD, as measured by the Patient Health Questionnaire (PHQ-9), the Generalized Anxiety Disorder-7 scale (GAD-7), and the Child PTSD Symptom Scale for DSM-5 (CPSS-5). Adolescents will be recruited from middle schools and randomly assigned to one of three groups: (a) psychoeducation, (b) psychoeducation + emotional skills enhancement, or (c) psychoeducation + emotional skills enhancement + positive childhood experience promotion. The school-based intervention will consist of 4-8 sessions, with assessments conducted at baseline, post-treatment, and a 3-month follow-up. Investigators will conduct multilevel models (MLMs) and structural equation models (SEMs) to investigate the impact of Adverse Childhood Experiences (ACEs), Positive Childhood Experiences (PCEs), alexithymia, and emotion regulation abilities on mental health outcomes in adolescents.

Trial Health

55
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
3,000

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

2 active sites

Status
active not recruiting

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 19, 2024

Completed
8 days until next milestone

Study Start

First participant enrolled

September 27, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 1, 2024

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2025

Completed
Last Updated

December 4, 2024

Status Verified

November 1, 2024

Enrollment Period

7 months

First QC Date

September 19, 2024

Last Update Submit

November 29, 2024

Conditions

Keywords

adolescentsrandomized controlled trialPTSDACEdepressionanxiety

Outcome Measures

Primary Outcomes (6)

  • Alexithymia

    A 36-item Peking alexithymia scale measures thoughts and behaviors that prevent people from feeling or recognizing negative emotions on a 5-point Likert scale (1 to 5, and total scores vary from 36 to 180). A higher score represents more severe alexithymia.

    baseline, post treatment(1 month), 3 month after post treatment

  • PTSD for adolescents

    The Child PTSD Symptom Scale for DSM-5 (CPSS-5) for adolescents and children (scores from 0 to 4, and total scores vary from 0 to 80). A higher score represents worse PTSD symptoms.

    baseline, post treatment(1 month), 3 month after post treatment

  • Emotion awareness

    A 30-item Emotion awareness questionnaire measures emotion awareness on a 3-point Likert scale (1 to 3, and total scores vary from 30 to 90). A higher score represents better emotion awareness.

    baseline, post treatment(1 month), 3 month after post treatment

  • Emotion regulation

    An 18-item cognitive emotion regulation questionnaire measures the ability of emotion regulation on a 5-point Likert scale (1 to 5, and total scores vary from 18 to 90). A higher score represents better emotion regulation.

    baseline, post treatment(1 month), 3 month after post treatment

  • Depression

    The 9-item patient health questionnaire (PHQ-9) for adults (score from 0 to 3, and total score varies from 0 to 27). A higher score represents worse depression symptoms.

    baseline, post treatment(1 month), 3 month after post treatment

  • Generalized anxiety disorder

    The Generalized Anxiety Disorder-7 scale (GAD-7) for adults, adolescents, and children (scored from 0 to 3, and total score from 0 to 21). A higher score represents worse anxiety symptoms.

    baseline, post treatment(1 month), 3 month after post treatment

Secondary Outcomes (4)

  • Irritability

    baseline, post treatment(1 month), 3 month after post treatment

  • Resilience

    baseline, post treatment(1 month), 3 month after post treatment

  • Seeking for help

    baseline, post treatment(1 month), 3 month after post treatment

  • Insomnia Severity

    baseline, post treatment(1 month), 3 month after post treatment

Other Outcomes (15)

  • Suicide

    baseline, post treatment(1 month), 3 month after post treatment

  • Self-esteem

    baseline, post treatment(1 month), 3 month after post treatment

  • Social support

    baseline, post treatment(1 month), 3 month after post treatment

  • +12 more other outcomes

Study Arms (3)

Psychoeducation group (PsyE)

ACTIVE COMPARATOR

Psychoeducation consists of parent and adolescent psychoeducation. The content includes an introduction to stress, emotional distress and mental disorders.

Behavioral: Psychoeducation

Psychoeducation + Emotional Skills (PsyE+EmoS)

EXPERIMENTAL

Psychoeducation includes sessions for both parents and adolescents, offering the same content as the control group, which introduces stress, emotional distress, and mental disorders. In addition, the emotional skills enhancement sessions provide online materials focused on emotional awareness and emotion regulation strategies, along with tasks related to the content. Participants will also be required to complete a weekly writing assignment, upload their written contents, and assess their level of subjective discomfort following each writing exercise.

Behavioral: Emotiaonl skill enhancementBehavioral: PCE promotionBehavioral: Psychoeducation

Psychoeducation + emotional skills + PCE (PsyE+EmoS+PoCE)

EXPERIMENTAL

In comparison to the PsyE+EmoS group, this group additionally requires parents to complete a weekly parent-child communication task aimed at fostering positive childhood experiences. Parents are also expected to document and upload the details of these tasks each week.

Behavioral: Emotiaonl skill enhancementBehavioral: Psychoeducation

Interventions

This intervention combines online material with practical, emotion-focused activities. Participants will receive training on emotional awareness and emotion regulation strategies, along with completing weekly writing assignments. These assignments focus on recent negative events and the emotions associated with them, encouraging emotional expression and processing.

Psychoeducation + Emotional Skills (PsyE+EmoS)Psychoeducation + emotional skills + PCE (PsyE+EmoS+PoCE)
PCE promotionBEHAVIORAL

The intervention requires parents to complete a weekly parent-child interaction task designed to foster positive childhood experiences. Parents will engage in structured activities with their children and document the interactions. Each week, they are expected to upload a report.

Psychoeducation + Emotional Skills (PsyE+EmoS)
PsychoeducationBEHAVIORAL

Psychoeducation includes sessions for both parents and adolescents, covering key topics such as stress, emotional distress, and mental disorders. The content provides foundational knowledge to help participants understand and manage these challenges.

Psychoeducation + Emotional Skills (PsyE+EmoS)Psychoeducation + emotional skills + PCE (PsyE+EmoS+PoCE)Psychoeducation group (PsyE)

Eligibility Criteria

Age10 Years - 18 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Middle school students studying in school and their parents
  • Capable of hearing, speaking, reading, and writing

You may not qualify if:

  • High suicidal risks
  • Severe mental disorders

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Biancun middle school

Baoding, Hebei, China

Location

Diannan middle school

Baoding, Hebei, China

Location

MeSH Terms

Conditions

Stress, PsychologicalStress Disorders, Post-TraumaticDepressionAnxiety Disorders

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorStress Disorders, TraumaticTrauma and Stressor Related DisordersMental Disorders

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 19, 2024

First Posted

October 1, 2024

Study Start

September 27, 2024

Primary Completion

April 30, 2025

Study Completion

July 31, 2025

Last Updated

December 4, 2024

Record last verified: 2024-11

Locations