Validation of the CIDI 5.0 Against the SCID-5 for Lifetime Mental Disorders

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorThe University of Hong Kong

About this trial

The World Health Organization Composite International Diagnostic Interview (CIDI) is a fully structured diagnostic tool designed for lay interviewers to assess the prevalence of mental and substance use disorders. Earlier versions, such as the CIDI 3.0, demonstrated acceptable individual-level concordance with clinical assessments based on DSM-IV criteria (Haro et al. 2006). The latest iteration (CIDI 5.0) has been updated to operationalize DSM-5 criteria.

Recent evidence from a large-scale, community-based national study in Qatar suggests that under DSM-5 criteria (Khaled et al. 2024), after recalibration, the CIDI 5.0 maintains high specificity (91.9% for MDD, 94.7% for GAD, and 85.5% for PTSD). Sensitivity suggested CIDI diagnoses aligned closely with clinical "gold standard" diagnoses (51.5% for MDD, 50.7% for GAD, and 77.3% for PTSD). Despite the evidence from Qatar, there remains a lack of evidence regarding the validity of the CIDI 5.0 in population-based studies.

Therefore, this study aims to evaluate the diagnostic validity of the CIDI 5.0 for Lifetime MDD, GAD, and PTSD, using the Structured Clinical Interview for DSM-5 (SCID-5) as the definitive clinical gold standard.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

Domestic workers

Trial population

This study is a sub-study of the District Health Profile (DHP), which is a district-level representative descriptive cross-sectional study. In DHP, 1% of households in selected Hong Kong districts will be randomly selected from the Census and Statistics Department's list of quarters, with stratification based on districts and housing types; all persons aged 18 and above in the recruited households will be included and surveyed. All individuals will complete the survey for the DHP study, including the CIDI-5 section. Based on prior studies (Haro et al., 2006; Khaled et al., 2024), to ensure adequate statistical power and control for Type I error, the clinical validation study will include 300 individuals. 77 participants will serve as controls with no history of mental disorders, and the remaining sample size will consist of participants with at least one lifetime diagnosis of MDD, GAD, or PTSD, as identified by CIDI-5, aiming to reach at least 112 samples for each diagnosis.

Trial design

Design model

Ecologic or community

Time perspective

Cross-sectional

Treatments tested in this trial

  • CIDI-5

    Diagnostic test

    The World Health Organization Composite International Diagnostic Interview-5th (CIDI-5) is a standardized diagnostic tool used to assess the prevalence of mental and substance use disorders over varying time frames (30 days, 12 months, and lifetime) based on the diagnostic criteria outlined in the Diagnostic and Statistical Manual of Mental Disorders 5th edition (DSM-5) and International Classification of Diseases 10th edition (ICD-10). Trained interviewers will administer selected modules from the Hong Kong version of the CIDI-5 in a computer-assisted personal interview to measure the outcomes. To validate the diagnoses in the CIDI-5 group, investigators will conduct clinical re-interviews of 3 selected CIDI-5 diagnoses: major depressive disorder (MDD), generalized anxiety disorder (GAD), and post-traumatic stress disorder (PTSD) using the Structured Clinician Interview for DSM-5 (SCID) by a trained mental health professional with previous experience using SCID.

Treatment groups

300 Participants
are divided into 1 treatment group
Group A: CIDI-5 Validation Cohort1 intervention

Trial outcomes

Primary outcomes

1

Depression

The main outcome in this module is the lifetime prevalence of Major Depressive Disorder (MDD)

Time frame
Immediately following intervention or recruitment
2

Worry and Anxiety

The main outcome in this module is the lifetime prevalence of Generalized Anxiety Disorder (GAD)

Time frame
Immediately following intervention or recruitment
3

Stressful Experiences

The main outcome in this module is the lifetime prevalence of PTSD.

Time frame
Immediately following intervention or recruitment

Secondary outcomes

Other outcomes

Sponsors and contacts

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