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Development of a Training Intervention to Improve Mental Health Treatment Effectiveness and Engagement for Youth With Documented Mental Health Disparities

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Boston College

Status

Completed

Conditions

Knowledge, Attitudes, Practice

Treatments

Behavioral: Training Intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05626231
Training Development Study
K23MH124670 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The overall goal of the larger 3-aim study is to develop and pilot test a training intervention to increase mental health providers' use of evidence-based practices with youth patients. Aim 3 (registered here) of the study is an open trial pilot study at a multi-clinic mental health agency, aimed at examining the feasibility and acceptability of conducting a future randomized controlled trial (RCT).

Full description

The overall goal of the larger 3-aim study is to develop and pilot test a training intervention to increase mental health providers' use of evidence-based practices with youth patients. The Boston College Institutional Review Board (IRB) approved protocol #21.247.01-15. Aim 1 involved designing the training intervention through an extensive literature review and community-engaged methods that centered on collaborations with providers, youth patients, and parents. Aim 2 (in progress) entails refining the training intervention via human centered design methods. Aim 3 (registered here) of the study is an open trial pilot study at a multi-clinic mental health agency, aimed at examining the feasibility and acceptability of conducting a future randomized controlled trial (RCT). Effectiveness and implementation data from both providers (n=49) and patients (i.e., youth and their parents; n=50 GMY and n=30 caregivers) will be collected and analyzed. Primary outcomes are measured at the provider-level and secondary outcomes are measured at the patient-level (i.e., patients and their parents).

Enrollment

286 patients

Sex

All

Ages

12+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

For provider participants:

  • Mental health care providers (e.g., psychologists, social workers) employed by the pilot site at the time of the pilot test and who work with clients ages 12-25
  • Age 18 or older
  • Fluent in English

For GMY participants:

  • Identify as a gender-minority.
  • Age 12-25
  • Currently receiving mental health services from the pilot site
  • Fluent in English

For parents of youth participants:

  • Parents of youth currently receiving mental health services at the pilot site
  • 18 or older
  • Fluent in English

Exclusion criteria

  • Provided that participants meet the aforementioned inclusion criteria, there are no explicit criteria for exclusion.

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

286 participants in 1 patient group

Training Intervention
Experimental group
Description:
The single-arm intervention study will test an online asynchronous evidence-based practices training intervention.
Treatment:
Behavioral: Training Intervention

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Maggi Price, PhD

Data sourced from clinicaltrials.gov

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