Clinical trial Recruiting at 5 sites Interventional Ages 12 to 14

Mental health program for at-risk adolescents in Malaysia

Official title: Promoting Mental Health Among At-risk Adolescents in Malaysia

Run by University of Roehampton · NCT07138664 · Data updated 2026-11-12

This will test a school-based program called Super Skills for Life against a study-skills control to see if it reduces anxiety and depression and improves wellbeing in 12–14-year-olds from low-income Malaysian communities.

Quick facts

Study typeInterventional
Ages12 Years to 14 Years
SexAll
Enrollment428 (estimated)
SponsorUniversity of Roehampton
Academic / other
Locations5 sites (Kota Kinabalu, Sabah and 4 other locations)
StatusRecruiting
StartedAugust 2025
Main results expectedSeptember 2026
Study endsSeptember 2026
Registry record updatedAugust 24, 2025
Trial IDNCT07138664 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adolescents aged 12–14 (Forms 1–2) in participating low-income Malaysian schools who score in the moderate-to-severe range on the DASS-21 and have parental consent, excluding those with diagnosed neurodevelopmental disorders or intellectual disability.

Probably not a fit

Students without moderate-to-severe anxiety or depression, those outside the 12–14 age range, those with excluded diagnoses, or those not attending participating schools are unlikely to benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This two-arm cluster randomized controlled trial compares the Super Skills for Life (SSL) program to a Study Skills Programme (SSP) control delivered in classrooms across at least 20 secondary schools serving low-income rural and urban communities in Malaysia. Adolescents aged 12–14 who screen with moderate to severe symptoms on the DASS-21 will be invited and classrooms randomized 1:1 with stratification by school size, class/form, and urban versus rural location. Primary outcomes are reductions in anxiety and depressive symptoms and improved mental wellbeing measured at baseline, immediately post-intervention (8 weeks), and at 6- and 12-month follow-ups, with the primary endpoint at 12 months; the protocol also includes cost-effectiveness and implementation analyses. The target sample is 428 adolescents (214 per arm) to provide adequate statistical power.

Why it matters

Potential benefit: If successful, the program could lower anxiety and depression symptoms and improve long-term wellbeing for vulnerable adolescents and be scaled across schools.

How similar studies have gone: School-based cognitive-behavioral programs, including prior implementations of Super Skills for Life, have shown positive effects on youth anxiety and depression in other countries, though results vary and evidence in low-income Malaysian settings is limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Adolescent (aged 12-14) who are in the first two years (Form 1 and Form 2, equivalent to year 7 and 8 in the United Kingdom school system, respectively) in lower secondary schools.
2. Adolescents score moderate to severe levels of anxiety and/or depression on the Depression Anxiety and Stress Scale-21 (DASS-21) based on the original cut-off norms (DASS-21 Anxiety scale ≥ 10 and/or DASS-21 Depression scale ≥ 14).
3. Adolescent's parent/carer provides written consent.

Exclusion Criteria:

(1) Being diagnosed with neurodevelopmental disorders. (2) Being diagnosed with intellectual disability.

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Where it's running

  • Fakulti Psikologi Dan Pendidikan
    Kota Kinabalu, Sabah, Malaysia
    Recruiting
  • Universiti Malaysia Sarawak
    Kuching, Sarawak, Malaysia
    Recruiting
  • Universiti Kebangsaan Malaysia
    Bangi, Selangor, Malaysia
    Recruiting
  • Universiti Malaya
    Kuala Lumpur, Selangor, Malaysia
    Recruiting
  • Sunway University
    Subang Jaya, Selangor, Malaysia
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.