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Clinical Trials/NCT06942637
NCT06942637CompletedNot Applicable

Effectiveness of Integrated Network for Student Psychosocial Intervention, Resilience, and Education (INSPIRE) on Mental Health Outcomes Among Indonesian Adolescents in Bandung: A Randomised Controlled Trial and Process Evaluation

National University of Singapore2 sites in 2 countries700 target enrollmentStarted: April 28, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
700
Locations
2
Primary Endpoint
Adolescents' mental health knowledge

Study Overview

Brief Summary

The INSPIRE (Integrated Network for Student Psychosocial Intervention, Resilience, and Education) intervention is an 8-week, school-based mental health program designed to enhance adolescents' mental health literacy and resilience while addressing symptoms of depression and anxiety. Implementation is conducted by school counselors who undergo an intensive two-day training program. The intervention is supported by comprehensive curriculum materials including detailed lesson plans, activities, discussion prompts, and instructional slides featuring key concepts, visuals, and explanatory content. Supplementary materials are developed for both participating adolescents and their parents.

The study aims to:

  1. Evaluate the usability and feasibility of the INSPIRE intervention within the school environment.
  2. Assess the intervention's effectiveness in improving:
  • Primary outcome: Mental health knowledge among adolescents
  • Secondary outcomes: Attitudes toward mental health, help-seeking behaviors, mental health literacy, resilience, and symptoms of depression and anxiety among adolescents
  • Secondary outcomes: mental health knowledge, attitudes, help-seeking behaviors, and mental health literacy among parents
  1. Explore the experiences of intervention participants (both adolescents and parents) against the control group to develop comprehensive insights into the psychosocial intervention's impact.

The research hypothesis proposes that the INSPIRE intervention group will demonstrate significantly higher scores in mental health knowledge, more positive attitudes toward mental health, increased help-seeking behaviors, enhanced mental health literacy, and greater resilience, while simultaneously showing reduced symptoms of depression and anxiety compared to the control group receiving standard care. These outcomes will be measured immediately following the intervention (post-test 1) and at one-month follow-up (post-test 2).

Detailed Description

Pilot Study The pilot study was conducted as a two-centre, two-arm cluster randomised controlled trial with a pre-test-post-test design and a 1:1 allocation ratio. Randomisation was performed at the school (cluster) level to minimise contamination. The pilot phase was implemented from 28 April to July 2025.

Randomised Controlled Trial (RCT) The full-scale randomised controlled trial expanded to a multi-centre design involving five centres, maintaining a two-arm cluster randomised structure with school-level allocation. The trial was conducted in two phases. Phase 1 randomised two schools (School 1 and School 2), with one allocated to the control group and the other to the intervention group. Phase 2 randomised three additional schools (Schools 3, 4, and 5) with a 1:2 allocation ratio (one to control, two to intervention) to address recruitment shortfalls.

The RCT commenced in September 2025. Participant recruitment and baseline data collection occurred between 12 September and 21 November 2025. Follow-up for primary and secondary outcomes was completed on 27 March 2026.

Process Evaluation Process evaluation was conducted from 18 December 2025 to 7 April 2026.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
13 Years to 15 Years (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Participants were initially restricted to students aged 13-15 years. However, the inclusion criteria in the RCT were subsequently broadened to encompass all junior high school students (grades 7-9) to ensure adequate recruitment and representativeness. Eligible students were required to be able to read, understand, and converse in Bahasa Indonesia.
  • •The inclusion criteria for parents are as follows:
  • •The biological father, mother, or an adult who fulfils a parental or guardian role for the participating adolescent
  • •Able to understand and communicate in Bahasa Indonesia.

Exclusion Criteria

  • •Adolescents who are working, clinically diagnosed with severe mental disorders, such as schizophrenia or psychosis, at high risk for mental health disorders (e.g., teenage pregnancy), or are cognitively impaired will be excluded.
  • •Parents with severe mental disorders or cognitive impairment that may hinder participation will be excluded.

Arms & Interventions

Standard school health routine care

No Intervention

INSPIRE Intervention

Experimental

Receive an 8-week school-based program aimed at enhancing adolescent mental health, attitudes towards mental health and help-seeking behaviors, mental health literacy, resilience and addressing depression and anxiety.

Intervention: INSPIRE (Integrated Network for Student Psychosocial Intervention, Resilience, and Education) (Behavioral)

Outcomes

Primary Outcomes

Adolescents' mental health knowledge

Time Frame: At one-month follow-up (post-test 2).

13-item mental health knowledge scale. Total scores range from 0 to 13, with higher scores indicating better mental health knowledge.

Adolescents' mental health knowledge

Time Frame: Immediately following the intervention (post-test 1)

13-item mental health knowledge scale. Total scores range from 0 to 13, with higher scores indicating better mental health knowledge.

Secondary Outcomes

  • Adolescents' attitudes towards mental health(At one-month follow-up (post-test 2).)
  • Adolescents' attitudes towards mental health(immediately following the intervention (post-test 1))
  • Adolescents' attitudes toward help-seeking behaviors(Immediately following the intervention (post-test 1))
  • Adolescents' mental health literacy(Immediately following the intervention (post-test 1))
  • Adolescents' resilience(Immediately following the intervention (post-test 1))
  • Adolescents' depression(Immediately following the intervention (post-test 1))
  • Adolescents' anxiety(Immediately following the intervention (post-test 1))
  • Parents' mental health knowledge(Immediately following the intervention (post-test 1))
  • Parents' attitudes towards mental health(immediately following the intervention (post-test 1))
  • Parents' attitudes toward help-seeking behaviors(Immediately following the intervention (post-test 1))
  • Parents' mental health literacy(Immediately following the intervention (post-test 1))
  • Adolescents' attitudes toward help-seeking behaviors(At one-month follow-up (post-test 2).)
  • Adolescents' mental health literacy(At one-month follow-up (post-test 2).)
  • Adolescents' resilience(At one-month follow-up (post-test 2).)
  • Adolescents' depression(At one-month follow-up (post-test 2).)
  • Adolescents' anxiety(At one-month follow-up (post-test 2).)
  • Parents' mental health knowledge(At one-month follow-up (post-test 2).)
  • Parents' attitudes towards mental health(At one-month follow-up (post-test 2).)
  • Parents' attitudes toward help-seeking behaviors(At one-month follow-up (post-test 2).)
  • Parents' mental health literacy(At one-month follow-up (post-test 2).)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Shefaly Shorey

Associate Professor

National University of Singapore

Study Sites (2)

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