Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
NCT06955195

Youth-for-Youth Mental Wellness Care and Action

Led by Chinese University of Hong Kong · Updated on 2025-08-28

18000

Participants Needed

2

Research Sites

123 weeks

Total Duration

On this page

Sponsors

C

Chinese University of Hong Kong

Lead Sponsor

N

New Life Psychiatric Rehabilitation Association

Collaborating Sponsor

AI-Summary

What this Trial Is About

This initiative aims to improve flourishing and quality of life of secondary school students, reduce mental distress (e.g., depression and suicidal ideation), enhance their understanding of mental health (e.g., mental health literacy) and help-seeking intention, and foster a supportive school environment (e.g., school climate-caring relationship, and sense of community). Also, this initiative aims to improve students' process of change in psychological (e.g., mattering, emotion regulation, empowerment) and social (e.g., trust belief) aspects and mental health awareness (e.g., mental health stigma). The feasibility, acceptability, and sustainability of the programme from multiple perspectives (e.g., students, student leaders, and stakeholders) will also be evaluated. In addition, the cost-effectiveness of delivering this programme (e.g., the incremental cost-effectiveness ratio (ICER)) among secondary schools in Hong Kong will be assessed. The programme will be implemented among students in 130 local secondary schools over three academic years. The first is a pilot phase (Year 1), which 40 schools will implement the intervention and student participants will be evaluated at pre- (T0) and post-intervention (T1) using questionnaires. In this stage, participatory research will be conducted before and after the intervention among students, student leaders, and stakeholders in 20 pilot schools to co-design the intervention, ensuring the programme meet the actual wellness needs of youth. In following two academic years, an additional 90 schools will participate in a cluster randomized controlled trial (RCT) with a 1:1 ratio between intervention and waitlist control groups. Each year, 45 schools will implement the intervention. Summative evaluation will be conducted among RCT schools at T0 and T1, and 3-month follow-up (T2). Quantitative data be collected to assess the effectiveness of intervention, and qualitative data will provide understanding of students' and stakeholders' perspectives of the intervention implementation. Cost outcomes will include intervention costs and cost savings, calculated from the payer (i.e., JC/government) perspective using administrative records or validated tools. The primary outcome of effectiveness will be the quality-adjusted life-years (QALYs) of students. Cost and QALYs will be used to evaluate the cost-effectiveness of the intervention, for example, estimate the incremental cost-effectiveness ratio (ICER).

CONDITIONS

Official Title

Youth-for-Youth Mental Wellness Care and Action

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Student in Hong Kong secondary school
  • Studying at Form 1 to Form 3 at the time of recruitment
  • Competence in comprehending written Chinese or English
  • Competence in speaking Cantonese or English
  • Written consent from students and their legal guardian
Not Eligible

You will not qualify if you...

  • Not studying at Form 1 to 3 in Hong Kong secondary school
  • Incompetence in comprehending written Chinese or English
  • Incompetence in speaking Cantonese or English
  • No written consent from students or their legal guardian

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 2 locations

1

Centre for Health Behaviours Research, JCSPHPC, CUHK

Hong Kong, HONG KONG, Hong Kong, 00000

Actively Recruiting

2

Centre for Health Behaviours Research, JCSPHPC, CUHK

Hong Kong, HONG KONG, Hong Kong, 00000

Actively Recruiting

Loading map...

Research Team

P

Phoenix Kit Han Mo, PhD

CONTACT

C

Calvin Lam, MSocSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here