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Trial record 3 of 234 for:    Recruiting, Not yet recruiting, Available Studies | "Mental Health"

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

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ClinicalTrials.gov Identifier: NCT03651050
Recruitment Status : Not yet recruiting
First Posted : August 29, 2018
Last Update Posted : August 29, 2018
Sponsor:
Information provided by (Responsible Party):
New York University School of Medicine

Brief Summary:
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.

Condition or disease Intervention/treatment Phase
Mental Health Behavioral: Faith Based Outreach (FBO) Behavioral: community-health-workers (CHW) Not Applicable

Detailed 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.


Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 331 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Implementing a Digital Child Mental Health Screening, Literacy, and Management Tool in Faith-Based Settings
Estimated Study Start Date : December 2018
Estimated Primary Completion Date : December 2018
Estimated Study Completion Date : December 2018

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Mental Health

Arm Intervention/treatment
Experimental: intervention FBOs receive the P-MHDT Behavioral: Faith Based Outreach (FBO)
Faith base outreach groups will be trained in P-MHDT

Experimental: control FBOs receive no P-MHDT Behavioral: community-health-workers (CHW)
COmmon health workers will be trained in P-MHDT




Primary Outcome Measures :
  1. Aggression measured by parent report [ Time Frame: 24 Months ]
  2. Anxiety measured by parent report [ Time Frame: 24 Months ]
  3. Depression measured by parent report [ Time Frame: 24 Months ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 90 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

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.

Responsible Party: New York University School of Medicine
ClinicalTrials.gov Identifier: NCT03651050     History of Changes
Other Study ID Numbers: 18-00728
First Posted: August 29, 2018    Key Record Dates
Last Update Posted: August 29, 2018
Last Verified: August 2018

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No