Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06087159

Promoting Mental Health of Teachers and Caregiver Using a Personalized mHealth Toolkit in Uganda

Led by NYU Langone Health · Updated on 2026-04-20

1180

Participants Needed

2

Research Sites

169 weeks

Total Duration

On this page

Sponsors

N

NYU Langone Health

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study record describes a two-phase of clinical trial study. The first phase is a pilot study phase (to study feasibility and efficacy of the intervention), and the second phase is an effectiveness study phase (a fully powered evaluation study to test the intervention effectiveness). This proposal seeks to develop and test a new mHealth intervention, the mHealth Toolkit for Wellness \& Empowering Lives of School Community (mWEL) in Uganda. The mWEL-digial toolkit is a preventive intervention tool for teachers and parents as a self-help support modality. Caregivers who need support in navigating the toolkit will be supported by peer-community health workers (P-CHWs).

CONDITIONS

Official Title

Promoting Mental Health of Teachers and Caregiver Using a Personalized mHealth Toolkit in Uganda

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Teachers must be teaching in recruited schools.
  • Participants must be at least 18 years old.
  • Parents must have a child aged 6 to 14 years.
Not Eligible

You will not qualify if you...

  • Severe psychopathology or cognitive impairment preventing consent or survey completion.
  • Not being a parent, teacher, or caregiver in one of the recruited primary schools.
  • Under 18 years old.
  • Not speaking English or Luganda.

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Study Site

Kampala, Uganda

Actively Recruiting

2

Study Site

Nakaseke, Uganda

Actively Recruiting

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Research Team

K

Keng-Yen Huang, PhD, MPH

CONTACT

D

Demy Kamboukos, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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