Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05863572

Strengthening Care in Collaboration With People With Lived Experience of Psychosis in Uganda

Led by George Washington University · Updated on 2025-06-19

132

Participants Needed

1

Research Sites

134 weeks

Total Duration

On this page

Sponsors

G

George Washington University

Lead Sponsor

Y

YouBelong Uganda

Collaborating Sponsor

AI-Summary

What this Trial Is About

Background: Mental health services are most effective and equitable when designed, delivered, and evaluated in collaboration with people with lived experience of mental health conditions. Unfortunately, people with lived experience are rarely involved in health systems strengthening or are limited to specific components (e.g., peer helpers) rather than multi-tiered collaboration in the continuum of health services (e.g., ranging from home- to community- to clinic-based services). Moreover, programs that do involve people with lived experience, typically involve people with a history of a substance use conditions or common mental disorders. In contrast, the collaboration of people with lived experience of psychosis is especially rare. A pilot cluster randomized controlled trial will be conducted in urban and peri-urban areas around Kampala, Uganda, to evaluate the benefits of an implementation strategy for mental health services with engagement of people with lived experience of psychosis throughout the home-to-community-to-clinic care continuum, this is a hybrid type-III implementation-effectiveness pilot focusing on the differences in implementation strategy. This implementation strategy, entitled "Strengthening CAre in collaboration with People with lived Experience of psychosis in Uganda", will include training people with lived experience of psychosis using PhotoVoice and other methods to participate at three levels: in-home services, community engagement, and primary health care facilities. The investigators will compare a standard task-sharing implementation arm using training by mental health specialists with an experimental implementation arm that includes collaboration with people with lived experience. The primary objective is to evaluate the feasibility and acceptability of this strategy in the context of assuring safety and wellbeing of people with lived experience of psychosis who collaborate in health systems strengthening. By collaborating on health systems strengthening across these multiple levels, we foresee a more in-depth contribution that can lead to rethinking how best to design and deliver care for people with lived experience of psychosis. Successful completion of this pilot will be the foundation for a fully powered trial to evaluate the benefits of multi-level collaboration with people with lived experience of psychosis.

CONDITIONS

Official Title

Strengthening Care in Collaboration With People With Lived Experience of Psychosis in Uganda

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • At least 18 years of age
  • Confirmed diagnosis of a primary psychotic disorder by a psychiatrist or psychiatric clinical officer
  • Completion of the YouBelongHOME (YBH) program
  • Provision of informed consent
  • Fluency in the local language (Luganda)
  • Good functioning in daily chores, family engagement, comprehension, and community participation as assessed by the YBH team
  • Having a supportive family member
  • Primary care providers must provide care in Kampala/Wakiso District and be selected by the facility in-charge
  • Community health workers must provide community-based health services in the same district and be selected by the facility in-charge
  • Patients diagnosed with psychosis at a primary care facility in Kampala/Wakiso District eligible for outpatient management
  • Patients or responsible surrogates must be able to consent to study enrollment and procedures
  • Family members or caregivers of patients above
Not Eligible

You will not qualify if you...

  • Facilitators unable to provide informed consent
  • Patients requiring inpatient management or services
  • Patients for whom consent cannot be obtained
  • Patients severely ill beyond the capacity of the health facility to treat
  • Family members who do not provide consent for participation

AI-Screening

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Trial Site Locations

Total: 1 location

1

YouBelong Uganda

Kampala, Uganda, 99999

Actively Recruiting

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Research Team

B

Brandon A Kohrt, MD, PhD

CONTACT

S

Sauharda Rai, MA,PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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