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A Mental Health Services Engagement Program for Racial and Ethnic Minority Young Adults

New York University (NYU) logo

New York University (NYU)

Status

Enrolling

Conditions

Psychosis
Bipolar and Related Disorders
Depressive Disorder

Treatments

Behavioral: Just Do You
Behavioral: Component A
Behavioral: Component B
Behavioral: Component C

Study type

Interventional

Funder types

Other

Identifiers

NCT06508450
K23MH132814 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Researchers aim to test a brief culturally-responsive young adult orientation program for community mental health services. They will conduct a 24-month randomized trial with 80 young adults from racial and ethnic minority groups in a community-based mental health clinic.

Full description

The study objective is to assess the feasibility and acceptability of three new culturally-responsive components added to the brief young adult engagement intervention called Just Do You. The new components incorporate techniques from the DSM-5 Cultural Formulation Interview (CFI) and creative arts therapy to increase culturally-responsive content in Just Do You, which demonstrated evidence of keeping young adults connected to their treatment in a prior trial. Components are designed to elicit relevant cultural characteristics, experiences, and perspectives of diverse young adults enrolled in psychiatric rehabilitation as part of the Just Do You orientation program. The investigators will examine whether the new culturally-responsive components improve engagement in mental health services and increase service utilization.

A total of 80 young adults enrolled in an outpatient psychiatric rehabilitation program in New York will be recruited over 24 months to take part in a randomized full factorial pilot trial. Participants will be given a baseline assessment and randomly assigned to one of eight combinations of intervention components. Just Do You will be delivered first to all participants, with the assigned combination of new components to follow. The intervention will be delivered at the psychiatric rehabilitation program and will last up to five weeks for each participant, depending on the experimental condition. Outcome measures will be assessed at baseline, post-intervention, and 3-month follow up.

Enrollment

80 estimated patients

Sex

All

Ages

18 to 34 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged 18-34
  • From groups other than non-Hispanic White
  • Enrolled in services at the partnering clinic site

Exclusion criteria

  • Cognitive impairments (i.e., young adult cannot understand consent process)
  • Unable to comprehend and speak English

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

80 participants in 8 patient groups

Just Do You
Active Comparator group
Description:
Just Do You Core Intervention
Treatment:
Behavioral: Just Do You
Just Do You-A
Experimental group
Description:
Just Do You plus Component A
Treatment:
Behavioral: Component A
Behavioral: Just Do You
Just Do You-B
Experimental group
Description:
Just Do You plus Component B
Treatment:
Behavioral: Component B
Behavioral: Just Do You
Just Do You-C
Experimental group
Description:
Just Do You plus Component C
Treatment:
Behavioral: Component C
Behavioral: Just Do You
Just Do You-AB
Experimental group
Description:
Just Do You plus Components A and B
Treatment:
Behavioral: Component B
Behavioral: Component A
Behavioral: Just Do You
Just Do You-AC
Experimental group
Description:
Just Do You plus Components A and C
Treatment:
Behavioral: Component C
Behavioral: Component A
Behavioral: Just Do You
Just Do You-CB
Experimental group
Description:
Just Do You plus Components C and B
Treatment:
Behavioral: Component C
Behavioral: Component B
Behavioral: Just Do You
Just Do You-ABC
Experimental group
Description:
Just Do You plus Components A B and C
Treatment:
Behavioral: Component C
Behavioral: Component B
Behavioral: Component A
Behavioral: Just Do You

Trial contacts and locations

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Central trial contact

Kiara L Moore, PhD

Data sourced from clinicaltrials.gov

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