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Implementing a Digital Child Mental Health Screening, Literacy, and Management Tool in Faith-Based Settings

NYU Langone Health logo

NYU Langone Health

Status

Completed

Conditions

Mental Health

Treatments

Behavioral: community-health-workers (CHW)
Behavioral: Faith Based Outreach (FBO)

Study type

Interventional

Funder types

Other

Identifiers

NCT03651050
18-00728

Details and patient eligibility

About

The proposed project is to develop a Pediatric-Mental Health Digital Toolkit (P-MHDT) Toolkit to support innovative child mental health preventive interventions in FBO settings. This project focuses on developing a P-MHDT and carrying out a pilot feasibility evaluation in real world settings. A group of Mental Health Professionals (MHPs)/ Community Healthcare Workers (CHWs) will be trained and the P-MHDT Toolkit intervention will be tested in 6 Faith Based Organizations (FBOs) in Uganda.

Full description

The specific aims of this proposed study include:

Aim 1. To develop a P-MHDT (by employing qualitative focus-group interviews and user-centered design to enhance usability).

Aim 2. To train mental health professionals and community health workers (CHWs) for the P-MHDT approach of child mental health promotion in Uganda (including monitoring impacts of training on CHWs' program implementation competency).

Aim 3 (11-24 month). To estimate impacts of the P-MHDT on FBOs and families (i.e., caregivers' mental health literacy, practices, and children's mental health) when implemented in the real world FBO settings.

Enrollment

319 patients

Sex

All

Ages

18 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Participants must be at least 18 years of age. Participating parents must be caregivers of age 1-7 years old children.
  • Children are not the subjects of this study, and will not participate in research activities.

Exclusion criteria

  • Evidence of psychopathology or cognitive impairment severe enough to preclude giving consent, or completing the survey instruments or the focus group of the study.
  • Minors (age <18) will also be excluded.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

319 participants in 2 patient groups

intervention FBOs receive the P-MHDT
Experimental group
Treatment:
Behavioral: Faith Based Outreach (FBO)
control FBOs receive no P-MHDT
Experimental group
Treatment:
Behavioral: community-health-workers (CHW)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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