- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04560348
Cognitive Behavioral Intervention and Adventure Training for Chinese University Students in Hong Kong
September 17, 2020 updated by: Jiayan Pan, Hong Kong Baptist University
Improving Mental Health by Cognitive Behavioral Intervention and Adventure Training for Chinese University Students in Hong Kong
This study developed an adventure-based cognitive behavioral intervention program for Hong Kong university student.
The program effectiveness was evaluated in reducing psychological distress and improving mental health of university students.
The 3-month maintenance effect was also tested.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
University students are vulnerable to mental health problems due to the various challenges they have to face in university life.
However, few studies have been conducted to evaluate the effectiveness of university counseling programs in Hong Kong.
This project aims at developing and systematically evaluating a culturally adapted and adventure-based cognitive behavioral intervention (aCBI) program to decrease psychological distress and improve various mental health outcomes for Chinese university students in Hong Kong.
The aCBI program was delivered in a form of general education course in a university setting.
Single group Pre-posttest design was adopted.The program was evaluated its effectiveness in reducing psychological distress, perceived stress, depressive and anxiety symptoms, negative thoughts and negative emotions and increasing positive thoughts and positive emotions.
Study Type
Interventional
Enrollment (Actual)
193
Phase
- Not Applicable
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
14 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- be of Chinese nationality
- be studying in undergraduate programs at Hong Kong Baptist University (HKBU), as the aCBI program will be provided in the form of a general education course at this university
- have GHQ-12 scores of 2-10 (0-0-1-1) (i.e., mild to moderate levels of psychological distress)
- be willing to complete the entire process of the project.
Exclusion Criteria:
- have GHQ-12 scores of 0-1 (i.e., a low level of psychological distress) or 11-12 (i.e., a high level of psychological distress)
- have one or more psychosis
- have experienced severe depression with suicidal attempts/ideation in the past 3 months, as diagnosed by a psychiatrist or a clinical psychologist.
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: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Adventure-based cognitive behavioral intervention
An adventure-based cognitive behavioral intervention program An 13-session adventure-based cognitive behavioral intervention program, including 6 lectures, 5 workshops and adventure games, and one adventure day camp (2 sessions).
One session per week, 3 hours for each session.
A variety of cognitive behavioral skills are taught in lectures and these skills are practiced in two groups (with appropriately 20 students in each group) in workshop to help students to apply these skills to cope with their own daily life stress.
The adventure training includes a day adventure camp and five 40-minute adventure games in the beginning of each workshop.
Skill briefing, case demonstration and debriefing, group sharing and discussion, in-class exercise and homework are used in the intervention program.
|
The adventure-based cognitive behavioral intervention is a combination of cognitive behavioral therapy and adventure training.
The intervention program is delivered in a 39-hour general education course in a public university in Hong Kong.
The program includes 6 lectures, 5 workshops, 5 adventure games and an adventure day camp.
Students are divided into two groups in workshop to practise CBT skills to deal with their own issues.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
General Health Questionnaire-12
Time Frame: baseline: before the intervention program starts
|
12-item rating scale for psychological distress, scale score ranges from 0-12, with a higher score indicating a higher level of psychological distress
|
baseline: before the intervention program starts
|
|
General Health Questionnaire-12
Time Frame: post-test: 1 month upon completion of the intervention program
|
12-item rating scale for psychological distress, scale score ranges from 0-12, with a higher score indicating a higher level of psychological distress
|
post-test: 1 month upon completion of the intervention program
|
|
General Health Questionnaire-12
Time Frame: 3-month follow-up test: 3 months after completion of the intervention program
|
12-item rating scale for psychological distress, scale score ranges from 0-12, with a higher score indicating a higher level of psychological distress
|
3-month follow-up test: 3 months after completion of the intervention program
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Stress Scale
Time Frame: baseline: before the intervention program starts
|
10-item rating scale for perceived stress, scale score ranges from 0-4, with a higher score indicating a higher level of perceived stress
|
baseline: before the intervention program starts
|
|
Perceived Stress Scale
Time Frame: post-test: 1 month upon completion of the intervention program
|
10-item rating scale for perceived stress, scale score ranges from 0-4, with a higher score indicating a higher level of perceived stress
|
post-test: 1 month upon completion of the intervention program
|
|
Perceived Stress Scale
Time Frame: 3-month follow-up test: 3 months after completion of the intervention program
|
10-item rating scale for perceived stress, scale score ranges from 0-4, with a higher score indicating a higher level of perceived stress
|
3-month follow-up test: 3 months after completion of the intervention program
|
|
Beck Depression Inventory
Time Frame: baseline: before the intervention program starts
|
21-item rating scale for depressive symptoms, scale score ranges from 0-63, with a higher score indicating a higher level of depressive symptions
|
baseline: before the intervention program starts
|
|
Beck Depression Inventory
Time Frame: post-test: 1 month upon completion of the intervention program
|
21-item rating scale for depressive symptoms, scale score ranges from 0-63, with a higher score indicating a higher level of depressive symptions
|
post-test: 1 month upon completion of the intervention program
|
|
Beck Depression Inventory
Time Frame: 3-month follow-up test: 3 months after completion of the intervention program
|
21-item rating scale for depressive symptoms, scale score ranges from 0-63, with a higher score indicating a higher level of depressive symptions
|
3-month follow-up test: 3 months after completion of the intervention program
|
|
Beck Anxiety Inventory
Time Frame: baseline: before the intervention program starts
|
21-item rating scale for anxiety symptoms, scale score ranges from 0-63, with a higher score indicating a higher level of anxiety symptoms
|
baseline: before the intervention program starts
|
|
Beck Anxiety Inventory
Time Frame: post-test: 1 month upon completion of the intervention program
|
21-item rating scale for anxiety symptoms, scale score ranges from 0-63, with a higher score indicating a higher level of anxiety symptoms
|
post-test: 1 month upon completion of the intervention program
|
|
Beck Anxiety Inventory
Time Frame: 3-month follow-up test: 3 months after completion of the intervention program
|
21-item rating scale for anxiety symptoms, scale score ranges from 0-63, with a higher score indicating a higher level of anxiety symptoms
|
3-month follow-up test: 3 months after completion of the intervention program
|
|
Automatic Thoughts Questionnaire
Time Frame: baseline: before the intervention program starts
|
14-item rating scale for positive and negative automatic thoughts, score ranges from 1-5 for the positive thought subscale and negative thought subscale, with a higher score indicating a higher level of positive/negative thought
|
baseline: before the intervention program starts
|
|
Automatic Thoughts Questionnaire
Time Frame: post-test: 1 month upon completion of the intervention program
|
14-item rating scale for positive and negative automatic thoughts, score ranges from 1-5 for the positive thought subscale and negative thought subscale, with a higher score indicating a higher level of positive/negative thought
|
post-test: 1 month upon completion of the intervention program
|
|
Automatic Thoughts Questionnaire
Time Frame: 3-month follow-up test: 3 months after completion of the intervention program
|
14-item rating scale for positive and negative automatic thoughts, score ranges from 1-5 for the positive thought subscale and negative thought subscale, with a higher score indicating a higher level of positive/negative thought
|
3-month follow-up test: 3 months after completion of the intervention program
|
|
Chinese Affect Scale
Time Frame: baseline: before the intervention program starts
|
20-item rating scale for positive and negative emotions, score ranges from 1-6 for positive emotion subscale and negative emotion subscale, with a higher score indicating a higher level of positive/negative emotion
|
baseline: before the intervention program starts
|
|
Chinese Affect Scale
Time Frame: post-test: 1 month upon completion of the intervention program
|
20-item rating scale for positive and negative emotions, score ranges from 1-6 for positive emotion subscale and negative emotion subscale, with a higher score indicating a higher level of positive/negative emotion
|
post-test: 1 month upon completion of the intervention program
|
|
Chinese Affect Scale
Time Frame: 3-month follow-up test: 3 months after completion of the intervention program
|
20-item rating scale for positive and negative emotions, score ranges from 1-6 for positive emotion subscale and negative emotion subscale, with a higher score indicating a higher level of positive/negative emotion
|
3-month follow-up test: 3 months after completion of the intervention program
|
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)
September 1, 2015
Primary Completion (Actual)
August 31, 2018
Study Completion (Actual)
August 31, 2018
Study Registration Dates
First Submitted
September 9, 2020
First Submitted That Met QC Criteria
September 17, 2020
First Posted (Actual)
September 23, 2020
Study Record Updates
Last Update Posted (Actual)
September 23, 2020
Last Update Submitted That Met QC Criteria
September 17, 2020
Last Verified
September 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- FRG2/14-15/090
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
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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