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NCT07627061
Integrated Motivational Interviewing and Rational Emotive Behavior Therapy Intervention for Non-Suicidal Self-Injury Among Malaysian Primary School Students: A Feasibility Trial Protocol
Conditions: Non-Suicidal Self-Injury, Emotional Dysregulation
Sex: All
Ages: 12 Years – 12 Years
Healthy volunteers: No
Phase: NA
Enrollment: 105
Sponsor: Universiti Utara Malaysia
Location: Selected Primary Schools in Kulim District Kulim Kedah
Summary
This study aims to evaluate the feasibility and preliminary effects of the MIND-SET Intervention Module, an integrated Motivational Interviewing and Rational Emotive Behavior Therapy (MI-REBT) intervention, among Malaysian primary school students involved in Non-Suicidal Self-Injury (NSSI) behaviour. The module is designed to reduce self-injurious behaviour, improve emotional regulation, and enhance readiness for change among 12-year-old students in school settings. This study will use a quasi-experimental design involving three groups: a MIND-SET intervention group, a PRISMA Mental Health Module group, and a treatment-as-usual group. Data will be collected at pre-intervention, post-intervention, and follow-up stages using validated psychological instruments. The findings are expected to support the development of culturally responsive, school-based mental health interventions for children involved in NSSI behaviour in Malaysia.
Eligibility Criteria
Inclusion Criteria:
* Primary school students aged 12 years old.
* Students identified with Non-Suicidal Self-Injury (NSSI) behaviour through school mental health screening and assessment procedures.
* Able to understand and participate in group counselling sessions.
* Written informed consent obtained from parents or guardians.
* Assent obtained from participating students.
Exclusion Criteria:
* Students currently receiving intensive psychiatric treatment or psychological -intervention for severe mental health conditions.
* Students identified with active suicidal intent requiring immediate clinical intervention.
* Students with severe cognitive or developmental impairments that may interfere with participation in group intervention activities.
* Students who are unable to attend the scheduled intervention sessions consistently.
Source: ClinicalTrials.gov (NCT07627061). StuddyBuddy aggregates publicly available trial information.