Efficacy of an electronic intervention for adolescent suicide attempters
Official title: A Multi-centric Trial to Evaluate the Efficacy of Electronic-Based Psychosocial Interventions on Future Suicide Risk Among Adolescent Suicide Attempters
Run by University of Pittsburgh · NCT06474221 · Data updated 2026-11-12
This study tests a new online program to help teenagers who have recently tried to harm themselves improve their coping skills and reduce the chances of future suicide attempts.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 12 Years to 18 Years |
| Sex | All |
| Enrollment | 168 (estimated) |
| Sponsor | University of Pittsburgh Academic / other |
| Locations | 2 sites (Bengaluru, Karnataka and 1 other locations) |
| Status | Recruiting |
| Started | August 31, 2024 |
| Main results expected | September 30, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | April 7, 2026 |
| Trial ID | NCT06474221 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adolescents aged 12-18 who have attempted suicide within the last thirty days and are medically stable.
✕Probably not a fit
Patients with current or lifetime diagnoses of psychosis, serious medical illnesses, or substance dependence may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the effectiveness of an Electronic Based Psychosocial Intervention (EBPSI) aimed at improving coping and problem-solving skills among adolescents who have recently attempted suicide. The research involves screening participants for eligibility, obtaining consent, conducting baseline assessments, randomizing participants, implementing the intervention, and performing follow-up assessments. The goal is to enhance accessibility to care and reduce future suicidal behavior in this vulnerable population.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce future suicide risk among adolescents who have attempted suicide.
How similar studies have gone: Other studies have shown promise in using electronic interventions for mental health, suggesting potential success for this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * All adolescents who have attempted suicide within the last thirty days and presented to the study site * Between ages of 12-18 years * Participants of all gender will be included * Medically stable patients who have stable blood pressure, breathing rates without fever, and intact orientation to time, place, and person Exclusion Criteria: * A current or a lifetime diagnosis of psychosis. We will confirm the same using a detailed clinical interview according to ICD-10 diagnostic guidelines. * A history of mental retardation and any neurological condition causing cognitive impairment. * 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. * A diagnosis of serious medical illness like end-stage cancer, AIDS, less than a month following acute cardiovascular and cerebrovascular events.
Where it's running
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St John's Medical College and Hospital
Bengaluru, Karnataka, India Recruiting -
Kalinga Institute of Medical Sciences (KIMS),
Bhubaneswar, Odisha, India Recruiting
Study contacts
- Principal investigator: Vishwajit L Nimgaonkar, MD, PhD — University of Pittsburgh
- Study coordinator: Vishwajit L Nimgaonkar, MD, PhD
- Email: vishwajitnl@upmc.edu
- Phone: 4127265164
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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SAFETY family-based program for youths after a suicide attempt
This project will test whether the SAFETY family-based therapy helps 10-17-year-olds who recently attempted suicide avoid repeat attempts.
-
Multi-layered digital monitoring and pharmacogenomics to prevent suicide in adults with depression
This study tests whether a digital monitoring system, a digital safety plan, and pharmacogenetic-guided care can reduce suicide re-attempts in adults with depression.
-
Mindfulness-based programs for suicidal thoughts and self-harm in Korean youth
We will test whether two mindfulness-based programs for Korean adolescents and young adults reduce suicidal thoughts, self-harm, depression, and problems with sleep and emotion regulation.
-
Youth suicide risk factors and personalized reduction strategies in young adults
This study tests whether combining clinical data, genetic information, neuroimaging, and microbiome data can help identify risk factors and see if a dTMS-based intervention reduces suicide risk in young adults with mood disorders.
-
Long-term follow-up of depression in psychiatric care
This project will follow 415 people with difficult-to-treat depression who were previously studied to see how their symptoms and treatment outcomes change over five years.
-
Improving coping to reduce suicide risk after ED discharge
This study tests whether an electronic safety plan and supportive text messages can help adults who have recently had suicidal thoughts or behaviors after leaving the emergency department.
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.