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Task-Shifting for Youth Suicide Prevention

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Boston College

Status

Begins enrollment in 5 months

Conditions

Adolescent Mental Health
Depressive Symptoms
Suicidal Ideation

Treatments

Other: Usual Community Center Services
Behavioral: Adapted Brief Interpersonal Psychotherapy for Adolescents (IPT-A LAZOS)

Study type

Interventional

Funder types

Other

Identifiers

NCT07383831
K23MH137405 (U.S. NIH Grant/Contract)
24.274

Details and patient eligibility

About

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.

Enrollment

46 estimated patients

Sex

All

Ages

12 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Parent consent
  2. Adolescent consent
  3. Enrolled in youth community centers
  4. Self-identified as Hispanic or Latine
  5. Between 12 and 17 years old.
  6. Scoring threshold for depression (4-9) as indicated in the PHQ-A.
  7. No current report of suicide ideation with plan or self-harming behaviors

Exclusion criteria

  1. Not consented to participate in the study
  2. Scoring 10 or higher in the PHQ-A, indicating depressive disorder
  3. Active suicide ideation (i.e., having thoughts of killing oneself, thinking about how in the past month).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

46 participants in 2 patient groups

Adapted IPT-A Delivered by Youth Mentors
Experimental group
Description:
Participants in this arm will receive 6 weekly sessions of an adapted, brief Interpersonal Psychotherapy for Adolescents (IPT-A) delivered by trained youth mentors (n=5) at the partnering youth community centers. The intervention focuses on improving interpersonal functioning, communication skills, and supportive relationships to reduce depressive symptoms, low belongingness, and perceived burdensomeness.
Treatment:
Behavioral: Adapted Brief Interpersonal Psychotherapy for Adolescents (IPT-A LAZOS)
Usual Community Center Services
Active Comparator group
Description:
Participants in this arm will continue to receive the standard youth programming and services offered at the participating community centers. This is an individual session focused on active listening.
Treatment:
Other: Usual Community Center Services

Trial contacts and locations

1

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Central trial contact

Carolina Vélez-Grau, PhD and LCSW; Krystel Francis, BA

Data sourced from clinicaltrials.gov

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