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NCT07383831
Task-Shifting for Youth Suicide Prevention
NA trial testing Adapted Brief Interpersonal Psychotherapy for Adolescents (IPT-A LAZOS) in Suicidal Ideation in 46 participants. Not yet recruiting.
1 December 2027
Quick facts
| Lead sponsor | Boston College |
|---|---|
| Phase | NA |
| Status | Not yet recruiting |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 46 |
| Start date | 1 August 2026 |
| Primary completion | 1 December 2027 |
| Estimated completion | 31 July 2028 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Adapted Brief Interpersonal Psychotherapy for Adolescents (IPT-A LAZOS)
- Usual Community Center Services
Conditions studied
- Suicidal Ideation — all drugs for Suicidal Ideation →
- Depressive Symptoms — all drugs for Depressive Symptoms →
- Adolescent Mental Health — all drugs for Adolescent Mental Health →
Sponsor
Boston College
Who can join
Adults 12 to 17, any sex, with Suicidal Ideation or Depressive Symptoms. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this randomized clinical trial is to examine the feasibility, acceptability, and mechanisms of change of a brief adaptation of Interpersonal Psychotherapy for Adolescents (IPT-A), adapted and task-shifted to lay providers (mentors, youth trusted adults) in youth community centers (YCCs) as an upstream approach to suicide. It focuses on Hispanic adolescents ages 12-17 enrolled in these YCCs. The pragmatic clinical trial will evaluate the acceptability and feasibility of adapted IPT-A delivered by mentors in YCCs and whether adapted IPT-A impacts mechanisms of change (depression symptoms, belongingness, and feeling like a burden to others). The main questions it aims to answer are: * Is adpated IPT-A, when delivered by trained youth mentors, feasible and acceptable in youth community centers? * Does adapted IPT-A target key risk factors (e.g., depressive symptoms, low belongingness, and perceived burdensomeness) associated with suicide ideation? Researchers will compare adolescents randomized to adapted IPT-A (6 sessions) delivered by a trained youth mentor with those receiving usual services at the community center (one individual session focused on active listening). Participants will: * Be screened for subthreshold depression using the PHQ-9 adolescent version. Adolescents will be included if they score between 4 and 9 (mild depression). Adolescents with a PHQ-9 score of 10 or higher will not be eligible and will be referred to a licensed mental health provider for appropriate care. * Be randomized to adapted IPT-A or usual care. * Youth in the intervention arm will participate in 6 weekly adapted IPT-A sessions with a trained youth mentor focused on education, affect identification, and interpersonal skills.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07383831
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07383831 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Boston College
- Last refreshed: 3 February 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07383831.
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