Actively Recruiting
Game Intervention for Resilience
Led by The University of Hong Kong · Updated on 2026-05-01
60
Participants Needed
1
Research Sites
22 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn if a game-based intervention can enhance psychological resilience and promote positive affectivity in adults who have experienced major life stress. The main questions it aims to answer are: * Does the game-based intervention improve positive affectivity and mental health compared to a waitlist control group immediately after the intervention and at 3-month follow-up? * Are the mental health benefits of the game-based intervention mediated by improvements in positive affectivity over time? Researchers will compare the game-based intervention to an active control group and a waitlist control group to see if the game leads to better emotional and mental health outcomes. Participants will: * Be randomly assigned to the game-based intervention group, the psychoeducation intervention group (as active control group), or the waitlist control group * Engage with the assigned program for 10 days within two weeks * Complete psychological assessments before and after the intervention, and again at 3-month follow-up
CONDITIONS
Official Title
Game Intervention for Resilience
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Fluency in oral and written Cantonese or Mandarin
- Experienced at least one major life stress in the past 5 years
- Normal or corrected-to-normal vision and hearing
You will not qualify if you...
- Formal diagnosis of any major psychiatric illnesses or history of suicidal behaviour
- Major physical illness, neurological condition, or traumatic brain injury
- Use of medication in the past 6 months that may affect emotion or cognitive functions
- Pregnancy (for women)
- Prior experience with any commercial computer repair simulation game
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
The University of Hong Kong
Hong Kong, Hong Kong
Actively Recruiting
Research Team
A
Associate Professor, Principle Investigator
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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