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Adolescentsâ?? Resilience and Treatment Needs for Mental Health in Indian Slums

Adolescentsâ?? Resilience and Treatment Needs for Mental health in Indian Slums - ARTEMIS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/02/040307
Enrollment
69600
Registered
2022-02-15
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: F949- Childhood disorder of social functioning, unspecified

Interventions

Intervention1: Anti-stigma and mhealth: Optimisation of anti stigma and mhealth intervention a.Antistigma component: System level interventions that reduce stigma, and upskill community health workers

Sponsors

The George Institute For Global Health
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All consenting adolescents in the age group of 10 â?? 19 years will be eligible for screening for CMDs to identify both a high risk and low risk cohort. Informed consent will be sought from all adult participants, and assent sought from minor participants following consent from their guardians. To be eligible for the high risk cohort participants must have at least one of the following: 1.High risk of depression based on a Patient Health Questionnaire-9 item (PHQ9) score >= 10 2.Positive response ( score >=2) to the suicide risk question on the PHQ-9

Exclusion criteria

Exclusion criteria: 1.Participants with severe ill-health that would prevent regular follow-up 2.Adolescents or their guardians do not provide informed written consent 3.Participants who are temporary residents of the slums

Design outcomes

Primary

MeasureTime frame
1. To change the mean behaviour scores at the end of the trial using the KAB scale 2. To assess the proportion of high risk achieving remission at end of trialTimepoint: 12 months

Secondary

MeasureTime frame
1.To change mean knowledge and attitude scores and change stigma perceptions of adolescents as assessed by BACE â?? TS Subscale 2.To change baseline mean stigma scores across both high and low risk cohorts 3. To assess standardised mean difference in PHQ-9 scores at end of trial 4.To assess the proportion at high risk of CMDs who have visited a doctor at least once between randomization and the end of the trial.Timepoint: 12 months

Countries

India

Contacts

Public ContactDr Pallab Maulik

George Institute For Global health

pmaulik@georgeinstitute.org.in911141588091

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 30, 2026