- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06623682
Study of Self-Help and Support Services for Student Mental Health in Tertiary Institutions
March 22, 2026 updated by: Winnie W.S. MAK, Chinese University of Hong Kong
Efficacy, Cost-effectiveness and Implementation of an Integrated Self-help and Support Services for Student Mental Health in Tertiary Institutions: JCTH+ Pragmatic Cluster RCT
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).
Study Overview
Status
Recruiting
Intervention / Treatment
Detailed 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.
Study Type
Interventional
Enrollment (Estimated)
1684
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Winnie WS Mak
- Phone Number: +852 3943 6577
- Email: wwsmak@cuhk.edu.hk
Study Contact Backup
- Name: Alan CY TONG, PhD
- Phone Number: +852 98117663
- Email: alantong@cuhk.edu.hk
Study Locations
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-
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Hong Kong, Hong Kong
- Recruiting
- Diversity and Well-being Lab
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Contact:
- Winnie WK Mak
- Phone Number: +852 3943 6577
- Email: wwsmak@cuhk.edu.hk
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: JCTH+-integrated mental health services
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.
|
Transdiagnostic cognitive behavioural therapy for both depression and anxiety that including modules from (1) Mindfulness-based intervention, (2) Rumination-focused cognitive behavioural therapy, and also including modules for insomnia and from Mindwork (Internet-based cognitive behavioural therapy).
|
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No Intervention: Service-as-usual (SAU)
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.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Recovery Quality of Life-20
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
It measures the quality of life in individuals with mental health conditions using a 5-point scale from 0 (none of the time) to 4 (most or all of the time).
It focuses on aspects crucial to those recovering from mental illness, such as well-being, self-perception, relationships, and activity.
Total scores ranged from 0 to 80, where higher scores indicated higher overall quality of life.
The scale is validated for its reliability and sensitivity in the Chinese-Hong Kong population, making it an effective tool for both clinical settings and research to track recovery progress and treatment outcomes in mental health in the local context.
|
Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Generalized Anxiety Disorder Assessment
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
It is a 7-item scale to assess the extent to which respondents are bothered by anxiety-related symptoms using a 4-point scale from 0 (not at all) to 3 (nearly every day).
Scores of 5, 10, and 15 denote the mild, moderate, and severe levels of anxiety respectively (range: 0-21).
At a cut-off of 10, GAD-7 has sensitivity of 0.89 and specificity of 0.82 in detecting generalized anxiety disorder (GAD).
The internal consistency of the Chinese version was 0.93.
|
Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
|
Patient Health Questionnaire
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
It includes 9 items to assess the extent to which respondents are bothered by depression-related symptoms using a 4-point scale from 0 (not at all) to 3 (nearly every day).
PHQ-9 has been validated and used widely in the general population for screening and measuring depression severity.
Scores of 5, 10, 15, and 20 denote mild, moderate, moderately severe, and severe levels of depression respectively (range: 0-27).
PHQ-9 has sensitivity of 0.88 and specificity of 0.88 in detecting major depressive disorder (MDD) at a cut-off of 10.
The internal consistency reliability of the Chinese version of the scale was 0.86.
|
Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
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Self-Stigma Of Seeking Help
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
It assesses the person's perception and reaction to seeking professional help using a 5-point scale from 1 (Strongly Disagree) to 5 (Strongly Agree).
The SSOH consists of 10 items.
Total scores ranged from 10 to 50, where higher scores indicate higher levels of self-stigma of seeking help.
The measurement demonstrated good reliability and validity in previous studies.
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Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
|
Youth Empowerment Scale-Mental Health
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
The individual level subscale was adopted, which contains 6 items to assess the level of self-empowerment in mental health using a 5-point scale from 0 (Never or almost never) to 5 (Always or almost always).
Total scores ranged from 6 to 30, where higher scores indicated higher level of ability in managing emotion and mental health.
The scale has demonstrated good internal consistency and construct validity.
|
Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
|
5-level EQ-5D version
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
The EQ-5D-5L comprises five dimensions, MOBILITY, SELF-CARE, USUAL ACTIVITIES, PAIN /DISCOMFORT and ANXIETY/ DEPRESSION, each dimension has five response levels: no problems, slight problems, moderate problems, severe problems, unable to/extreme problems.
The respondent is asked to indicate his/her health state by checking the box next to the most appropriate response level for each of the five dimensions.
Responses are coded as single-digit numbers expressing the severity level selected in each dimension.
The digits for the five dimensions can be combined in a 5-digit code that describes the respondent's health state; for instance, 21111 means slight problems in the mobility dimension and no problems in any of the other dimensions.
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Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
|
Nonattachment Scale-Short Form
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
Nonattachment Scale-Short Form (NAS-SF) includes 8 items to measure nonattachment using a 6-point Likert scale from 1 (strongly disagree) to 6 (strongly agree).
Total scores ranged from 8 to 48, where higher scores indicated higher levels of nonattachment.
It yielded satisfactory internal consistency and validity.
|
Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
|
General Mattering Scale
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
The 5-item General Mattering Scale measures perceptions and feelings of being important to other people (e.g., "How much would you be missed if you went away?").
Items are rated on a scale ranging from 1 (Not at all) to 4 (A lot) with good reliability and validity.
Total scores ranged from 5 to 20, where higher scores indicated higher level of mattering.
|
Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
|
Anti-Mattering Scale
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
The Anti-Mattering Scale is a five-item scale ranging from 1 (Not at all) to 4 (A lot) assessing the degree to which people feel like they do not matter to others.
Sample item include "To what extent have you been made to feel like you are invisible?".
Total scores ranged from 5 to 20, where higher scores indicated lower levels of mattering.
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Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
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Perceived Competence
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
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It contains 4 items on a 7-point Likert scale from 1 (none at all) to 7 (very true) to assess the self-perceived competence in maintaining regular self-care.
Total scores ranged from 4 to 28, where higher scores indicated higher levels of self-perceived competence in maintaining regular self-care.
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Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
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Treatment Self-regulation Questionnaire
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
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It contains 15 items on a 7-point Likert scale from 1 (not true at all) to 5 (completely true) to understand the reason for beginning or keeping regular mental self-care.
Higher scores in each item indicate higher importance of the reason for keeping mental self-care.
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Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
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Mindful Self-Care Scale
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
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The scale utilizes a 6-point Likert scale, ranging from 0 = never to 4 = regularly, to measure self-care in six factors: physical care, supportive relationships, mindful awareness, self-compassion and purpose, mindful relaxation, and supportive structure.
A higher score indicates a higher frequency of engaging in mindful self-care within the past week.
The scale demonstrates adequate reliability with Cronbach's coefficient alphas equal to 0.89 for the total 33-item.
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Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
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College Self-Efficacy Inventory
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
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It evaluates the self-efficacy of college students in academic settings.
It consisted of 20 items that load into three subscales: Course Efficacy, Social Efficacy, and Roommate Efficacy.
In this study, only 16 items on Course Efficacy, Social Efficacy will be included since dormitory is not usually available for students at post-secondary institutions.
The confidence level is measured by using a scale ranging from 1 (Not confident at all) to 10 (Extremely confident).
Higher scores in each subscale demonstrate a higher level of self-efficacy in that dimension.
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Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
|
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Basic Psychological Need Satisfaction in General
Time Frame: Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
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It contains 21 items to measure basic psychological need satisfaction in 3 subscales: Autonomy, Competence, and Relatedness.
The scale used a 7-point Likert scale from 1 (not at all true ) to 7 (very true).
Higher scores in each subscale indicated a higher degree to which the person experiences satisfaction with each of the three needs.
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Baseline, 4 months, 8 months, 12 months, 16 months, 20 months and 24 months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 9, 2024
Primary Completion (Estimated)
August 29, 2026
Study Completion (Estimated)
August 29, 2026
Study Registration Dates
First Submitted
September 20, 2024
First Submitted That Met QC Criteria
September 30, 2024
First Posted (Actual)
October 2, 2024
Study Record Updates
Last Update Posted (Actual)
March 24, 2026
Last Update Submitted That Met QC Criteria
March 22, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SBRE-23-0966A
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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