Actively Recruiting
No Time to Wait: Single Session Intervention
Led by United Christian Hospital · Updated on 2026-02-03
124
Participants Needed
1
Research Sites
59 weeks
Total Duration
On this page
Sponsors
U
United Christian Hospital
Lead Sponsor
H
Hong Kong University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Mental health problems in youth are prevalent, but early intervention effectively reduces symptoms, substance abuse risk, suicide, and comorbidities. In Hong Kong, however, only 26% of people with common mental disorders seek services (Lam et al., 2015), and even then, they face long delays-e.g., 90 weeks (90th percentile) for stable cases in public psychiatry clinics (Hospital Authority, 2024). Barriers include high costs, transportation issues, stigma, and preference for self-help, creating a strong need for scalable, accessible digital solutions, especially for youth. Single-Session Interventions (SSI) offer promise as brief, time-efficient tools that provide immediate support with minimal engagement burden. Online SSIs are often free, publicly available, and evidence-based. Research shows they reduce symptoms (moderate effect size Hedges' g = 0.32; 58% chance of better outcome vs. control), improve functioning, and boost satisfaction (Schleider \& Weisz, 2017). They work well for specific phobias and acute stress. Yet, their real-world acceptability, effectiveness outside trials, and integration with public services remain understudied-particularly for children/adolescents on waitlists. This pilot study evaluates an online single-session psychotherapy for youth (children/adolescents) on Hong Kong public psychotherapy waitlists, targeting depression and anxiety symptoms. It extends prior work by: Targeting two key constructs prominent in Asian contexts: Alexithymia - difficulty identifying/describing emotions; affects \~10% generally but 36% of Hong Kong adolescents (higher in females). It worsens depression, lowers well-being, complicates therapy, and reduces help-seeking. Fixed mindset (vs. growth mindset) - Asian groups show lower growth mindset levels; growth mindset buffers mental health issues (meta-analysis r = -0.220 with anxiety/depression/stress) and promotes better emotional regulation and treatment engagement. Examining how SSI influences acceptability and expectancy toward subsequent face-to-face psychotherapy. Hypotheses: SSI will reduce depression/anxiety symptoms more than treatment-as-usual. SSI will increase acceptability and positive expectancy for future in-person treatment. Change mechanisms-perceived behavioral control and emotional control-will mediate and sustain post-intervention outcomes. Overall, the study aims to test SSI as a bridge intervention to bridge service gaps, address culturally relevant barriers, and inform scalable mental health strategies in resource-constrained settings like Hong Kong's public system.
CONDITIONS
Official Title
No Time to Wait: Single Session Intervention
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be a Hong Kong resident aged 12 to 17 years
- Have anxiety and/or depression symptoms with a score of 10 or above on PHQ-9 or GAD-7
- Have access to the internet and a valid email address
- Be able to understand and read Chinese
- Have parent or legal guardian willing to provide informed consent
You will not qualify if you...
- Received psychological treatment for depression or anxiety in the past 3 months
- Diagnosed with severe psychiatric disorders such as psychotic disorder, bipolar disorder, dissociative disorder, or other neurocognitive disorders
- Participating in another similar study at the same time
- Report suicidal thoughts (score > 2 on Question 9 of Beck Depression Inventory)
- History of substance abuse
- Changed psychotropic medication within 2 weeks before baseline assessment
- Pregnancy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
United Christian Hospital
Hong Kong, Hong Kong
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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