Actively Recruiting

Phase Not Applicable
Age: 12Years - 18Years
All Genders
ID06474221

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

Led by University of Pittsburgh · Updated on 2026-04-07

168

Participants Needed

2

Research Sites

13 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

F

Fogarty International Center of the National Institute of Health

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to evaluate the effectiveness of an electronic psycho-social intervention designed to improve coping and problem-solving skills to reduce suicidal behavior among adolescents who have attempted suicide. The study targets adolescents aged 12 to 18 years and seeks to bridge gaps in access to care for those at risk of suicide. It is a randomized controlled trial comparing two approaches to support this vulnerable group. Participants will be randomly assigned to one of two groups: one group receives an electronic psycho-social intervention via video-based telepsychiatry sessions focused on brief interventions and coping skills, delivered in five sessions on days 10, 30, 45, 60, and 90 after initial assessment. The other group receives treatment as usual, consisting of five regular telephonic reminder calls on the same schedule, providing emotional support and reminders for follow-up. Both groups are followed over a one-year period. Participants undergo screening for eligibility, provide consent, and complete baseline assessments using several standardized questionnaires. Follow-up assessments occur at 1, 3, 6, and 12 months post-intervention, measuring outcomes such as persistent suicidal thoughts, suicide attempts, depression, and coping ability. The study includes careful monitoring and data collection to ensure proper conduct and evaluation of the interventions. The total duration of involvement for each participant is up to one year after the baseline intervention.

CONDITIONS

Brief Title

Efficacy of EBPSI on Future Suicide Risk Among Adolescent Suicide Attempters

Who Can Participate

Age: 12Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adolescents aged 12 to 18 years
  • Have attempted suicide within the last 30 days and presented to the study site
  • Includes participants of all genders
  • Medically stable with normal blood pressure, breathing rates, no fever, and full orientation to time, place, and person
Not Eligible

You will not qualify if you...

  • Current or lifetime diagnosis of psychosis as per ICD-10 criteria
  • History of mental retardation or neurological conditions causing cognitive impairment
  • Diagnosis of substance dependence (excluding tobacco) within the last six months
  • Serious medical illness such as end-stage cancer, AIDS, or recent acute cardiovascular or cerebrovascular events within one month

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Baseline Assessment

Duration - 1 day

Participants complete baseline assessments including questionnaires and clinical scales after consent and eligibility confirmation.

1 baseline visit (in-person)

Treatment

Duration - 90 days

Participants receive either video-based telepsychiatry sessions focused on brief intervention and coping skills, or telephonic supportive psychotherapy calls as usual care.

5 scheduled sessions on days 10, 30, 45, 60, and 90 after baseline intervention (video or phone)

Follow-up

Duration - 12 months

Participants complete follow-up assessments at 1, 3, 6, and 12 months after baseline intervention to monitor outcomes and intervention acceptability.

4 follow-up visits for assessments at 1, 3, 6, and 12 months

Trial Site Locations

Total: 2 locations

1

St John's Medical College and Hospital

Bengaluru, Karnataka, India, 560034

Actively Recruiting

2

Kalinga Institute of Medical Sciences (KIMS),

Bhubaneswar, Odisha, India, 751024

Actively Recruiting

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Research Team

V

Vishwajit L Nimgaonkar, MD, PhD

T

Triptish Triptish, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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