CIDI 5.0 validation against SCID-5 for lifetime mental disorders in Hong Kong adults
Official title: Validity of the World Health Organization CIDI 5.0 for Assessing Lifetime Prevalence of Mental Disorders: A Clinical Reappraisal Study Using the SCID-5
Run by The University of Hong Kong · NCT07604753 · Data updated 2026-11-12
This study tests whether the CIDI 5.0 interview can reliably identify lifetime mental disorders in adults in Hong Kong by comparing it with the SCID-5 diagnostic interview.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 300 (estimated) |
| Sponsor | The University of Hong Kong Academic / other |
| Locations | 1 site (Hong Kong) |
| Status | Recruiting |
| Started | May 14, 2025 |
| Main results expected | January 2028 |
| Study ends | January 2028 |
| Registry record updated | May 22, 2026 |
| Trial ID | NCT07604753 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults 18+ who reside in Hong Kong, can read Chinese or English, and do not have cognitive or linguistic barriers.
✕Probably not a fit
Participants unable to complete interviews in Chinese or English or with cognitive difficulties may receive limited diagnostic insight from the interview.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study evaluates the validity of the CIDI 5.0, a structured diagnostic interview, against the SCID-5 gold standard for lifetime mental disorders (MDD, GAD, PTSD) in a population-based sample in Hong Kong. Randomly sampled adults 18+ from local housing are assessed in Chinese or English. The study leverages updated DSM-5 criteria and prior Qatar data to examine specificity and sensitivity of CIDI 5.0 in real-world settings. Outcomes focus on concordance with clinical diagnoses and potential applicability for large-scale epidemiological research. The design emphasizes population-based validity rather than clinical treatment effects.
Why it matters
Potential benefit: If successful, CIDI 5.0 could be a reliable, cost-effective tool for large-scale mental health surveys and epidemiology in Hong Kong.
How similar studies have gone: Prior international studies showed varying concordance; this study builds on Qatar findings and aims to establish validity in a new population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * All household members aged 18 years old and over are randomly sampled from the Census and Statistics Department List of Quarters * Live in the address sampled from the Census and Statistics Department List of Quarters * Reside in Hong Kong for at least six months in the past year * Able to read and communicate in Chinese or English * Without linguistic or cognitive difficulties Exclusion Criteria: * Domestic workers
Where it's running
-
The University of Hong Kong
Hong Kong, Hong Kong Recruiting
Study contacts
- Study coordinator: Yoona Kim, PhD
- Email: yoonak@hku.hk
- Phone: +852 3917 9109
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.