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Study of Self-Help and Support Services for Student Mental Health in Tertiary Institutions

The Chinese University of Hong Kong logo

The Chinese University of Hong Kong

Status

Enrolling

Conditions

Self-care
Psychological Intervention
Mental Well-being
Mental Health

Treatments

Behavioral: Transdiagnostic cognitive behavioural therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06623682
SBRE-23-0966A

Details and patient eligibility

About

This proposed study aims to evaluate the implementation of integrating the existing services in tertiary education institutions with the JCTH+ platform. The study aims to evaluate the efficacy of JCTH+ on students' mental health outcomes as compared to service as usual, and to assess the cost-utility of the platform to determine whether the benefits of implementing the platform justify the costs associated. It is hypothesized that participants who receive integrated self-help and support services will show (H1) a greater reduction in mental health symptoms, and (H2) better mental well-being compared with participants in the control condition, i.e. service-as-usual (SAU).

Full description

This study is a parallel pragmatic cluster-randomized control trial evaluating the efficacy and cost-utility of a JCTH+-integrated services, as compared to service-as-usual among tertiary education institutions in Hong Kong. Randomisation will be carried out at institution level based on a computer-generated sequence. The estimated sample size will be 1,684, with 842 participants per condition. A factorial design will be adopted with all eligible participants completing assessments at 7 timepoints: baseline, 4 months post-test, 8-, 12-, 16-, 20- and 24-months follow-up. The primary endpoint is 4 months at post-test after baseline assessment. Concurrently, all staff involved in the project will be interviewed qualitatively at 12 months and 24 months from enrolment to understand their experience in the integration process and effectiveness of implementation.

Enrollment

1,684 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years old or above
  • Able to read Chinese or English
  • With internet connection and able to access the internet
  • With moderate-severe GAD-7 a/o moderate-severe PHQ-9
  • studying full-time at a tertiary education institution in Hong Kong

Exclusion criteria

  • not able to read and understand Chinese;
  • under 18 years old;
  • not able to access the Internet or use digital devices
  • without depressive symptoms or anxiety symptoms

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

1,684 participants in 2 patient groups

JCTH+-integrated mental health services
Experimental group
Description:
In the intervention arm, the JCTH+ platform will be integrated into the existing services of tertiary education institutions and introduced to students through mass advertisement within the institution. After randomization, three tertiary education institutions are allocated in this arm, including Chinese University of Hong Kong (CUHK), University of Hong Kong (HKU), and Hong Kong University's School of Professional and Continuing Education (HKU SPACE). Students will be invited to join this study and give consent adhering to the declaration of Helsinki.
Treatment:
Behavioral: Transdiagnostic cognitive behavioural therapy
Service-as-usual (SAU)
No Intervention group
Description:
In the no-intervention group, participants will continue with their usual practice, i.e. service-as-usual (SAU), for 4 months before implementing the project. After randomization, three tertiary education institutions are allocated in this arm, including The Hong Kong Polytechnic University (PolyU), Tung Wah College (TWC) and City University of Hong Kong (CityU). The same integration procedure will be implemented after this waiting period.

Trial contacts and locations

1

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Central trial contact

Kai Lam Cheng; Winnie WS MAK

Data sourced from clinicaltrials.gov

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