Skip to content

Video consultation based Interventions to reduce Future Suicide Risk among Adolescents who attempted Suicide.

A Multi-centric Trial to Evaluate the Efficacy of Electronic-Based Psychosocial Interventions on Future Suicide Risk among Adolescent Suicide Attempters.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/063011
Enrollment
168
Registered
2024-02-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: R458- Other symptoms and signs involvingemotional state Health Condition 2: T149- Unspecified injury

Interventions

Intervention1: Electronic based Psycho-social Intervention (EBPSI): The video-based telepsychiatry consultations shall include a total of 5 sessions on days 10, 30, 45, 60 and 90 after baseline interv

Sponsors

National Institutes of Health
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All adolescents who have attempted suicide within the last thirty days and presented to the study site 2. Between ages of 12–18 years 3. Participants of all gender will be included 3. Medically stable patients who have stable blood pressure, breathing rates without fever, and intact orientation to time, place, and person

Exclusion criteria

Exclusion criteria: 1. A current or a lifetime diagnosis of psychosis. We will confirm the same using a detailed clinical interview according to ICD-10 diagnostic guidelines. 2. A history of mental retardation and any neurological condition causing cognitive impairment. 3. A diagnosis of substance dependence as confirmed by M.I.N.I. KID 6.0 over the last six months. We will include those with tobacco dependence. 4. A diagnosis of serious medical illness like end-stage cancer, AIDS, less than a month following acute cardio-vascular and cerebrovascular events.

Design outcomes

Primary

MeasureTime frame
Primary outcome measures will be group comparisons on persistent suicidal ideation using the Columbia Suicide Severity Rating Scale (C-SSRS) and number of repeat suicide attempts.Timepoint: Baseline, 1 month, 3 months and 6 months

Secondary

MeasureTime frame
Secondary outcome measures will be group comparisons on depression (BDI), the acceptability of interventions using Acceptability of Intervention Measure (AIM), Intervention Appropriateness Measure (IAM) and Feasibility of Intervention Measure (FIM), assess the attributional style using Children’s Attributional Style Questionnaire and coping mechanism using BRIEF – COPE – Brief Coping QuestionnaireTimepoint: Baseline, 1 month, 3 months and 6 months

Countries

India

Contacts

Public ContactDr Suhas Chandran

KIMS, KIIT University, Bhubaneswar

drjigyansaipsita@gmail.com8093515161

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026