Improving Screening and Follow Up for Suicidal Ideation and Behaviors Among Latinx Youth in Primary Care

NCT ID: NCT06229223

Last Updated: 2025-05-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

250 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-03-26

Study Completion Date

2026-09-30

Brief Summary

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The objective of this proposal is to develop and pilot a systems-level strategy in pediatric primary care to enhance identification and management of suicidal ideation and behavior in Latinx youth, particularly those in immigrant families with parents who have limited English proficiency (LEP). The investigators will focus on the use of trained community health workers (CHWs) to increase clinic capacity and quality of suicide risk screening and early intervention, with a focus on safety planning, parent psychoeducation and care coordination.

Specific aims are 1: To develop site-specific implementation protocols for the integration of CHWs into SIB screening and safety planning for Latinx youth and the youths families; 2: To pilot the implementation of the program in a six-month open trial in four pediatric primary care practices representing a range of usual practice settings; and 3: To engage a stakeholder network to explore barriers and facilitators, including costs and billing strategies, to implementation of this approach across a broad range of pediatric primary care settings.

Parents/guardians of youth who have been referred to and agree to participate in the intervention by the child's primary care provider will participate in a 2-month program consisting of 6-8 phone sessions with a community health worker focusing on safety planning, information/education, program solving and self-care. Research participants will be asked to complete a survey via phone at the beginning of the program and another at the end of the program. The participants may also be asked to participate in an additional interview about the study.

Detailed Description

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Conditions

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Suicidal Ideation

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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PALOMA

Parents/guardians of youth who have been referred to and agree to participate in the intervention by the child's primary care provider will participate in a 2-month program consisting of 5-7 phone sessions with a community health worker focusing on safety planning, information/education, program solving and self-care. Research participants will be asked to complete a survey via phone at the beginning of the program and another at the end of the program. The participants may also be asked to participate in an additional interview about the participants experience during the study.

Group Type EXPERIMENTAL

PALOMA

Intervention Type BEHAVIORAL

Partnering with Parents of Adolescent Latinos on Mental Health Assistance

Interventions

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PALOMA

Partnering with Parents of Adolescent Latinos on Mental Health Assistance

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Youth has history of suicidal ideation/behavior or non-suicidal self-harm and
* Youth identifies as Latino/Latinx/Hispanic/Latin American and
* Guardian(s) speaks Spanish

Exclusion Criteria

* None
Minimum Eligible Age

10 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute of Mental Health (NIMH)

NIH

Sponsor Role collaborator

Johns Hopkins University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Sarah Polk, MD

Role: PRINCIPAL_INVESTIGATOR

Johns Hopkins School of Medicine

Locations

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BMS at Yard 56

Baltimore, Maryland, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Ellen Molino

Role: CONTACT

14105509019

Sarah Polk, MD

Role: CONTACT

4105504114

Facility Contacts

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Sarah Polk, MD

Role: primary

Other Identifiers

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R34MH129771

Identifier Type: NIH

Identifier Source: secondary_id

View Link

IRB00378575

Identifier Type: -

Identifier Source: org_study_id

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