Clinical trial No longer in our active list Interventional Ages 18 and up

Support and care for people with psychosocial disabilities in Africa

Official title: SUCCEED Africa: Protocol for a Multi-method Pilot Study of a Community-based Intervention for People With Psychosis in West and Southeast Africa

Run by London School of Hygiene and Tropical Medicine · NCT06007105 · Data updated 2026-05-14

This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.

This study is testing a new community support program for adults with psychotic disorders in sub-Saharan Africa to see if it can help them manage their symptoms and improve their social lives.

More Schizophrenia trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment40 (estimated)
SponsorLondon School of Hygiene and Tropical Medicine
Academic / other
Locations4 sites (Blantyre, Southern and 3 other locations)
Trial IDNCT06007105 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18 and older with a current or past diagnosis of a primary psychotic disorder who can communicate in one of the study's main languages.

Probably not a fit

Patients who do not have a diagnosis of a psychotic disorder or who are unable to participate due to language barriers may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This initiative aims to provide comprehensive community-based interventions for individuals experiencing psychotic disorders in sub-Saharan Africa. It focuses on addressing not only the clinical symptoms of conditions like schizophrenia and delusional disorder but also the social challenges faced by these individuals, such as poverty and unemployment. The program is designed to empower participants through peer support and co-production, ensuring that interventions are culturally appropriate and accessible. The study will involve participants who are adults with a diagnosis of psychosis, utilizing both health records and diagnostic interviews for eligibility.

Why it matters

Potential benefit: If successful, this program could significantly improve the quality of life and social integration for individuals with psychotic disorders in low-resource settings.

How similar studies have gone: While there have been few studies focusing on community-based rehabilitation for psychosocial disabilities in Africa, this approach is largely novel and aims to fill a significant gap in the existing literature.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion criteria:

Participants with lived experience of psychosis must:

* Be consenting/assenting adults (age 18+)
* Be able to speak one of the main study languages: English, Chichewa, Krio, Shona, Yoruba
* Live within the pilot study area
* Have a current or past diagnosis of schizophrenia or other primary psychotic disorder, bipolar or depressive disorder with psychotic symptoms, or a maternal mental health or behavioural disorder with psychotic symptoms, as per the World Health Organisation's International Classification of Diseases Version 11 (see full list of eligible diagnoses, below).

For participants recruited from within the health care system, diagnosis will be confirmed from health records. For those identified in the community, a research worker will administer the World Health Organisation's Composite International Diagnostic Interview (WHO CIDI) screening tool for psychosis.

The following diagnoses are eligible for inclusion:

* Schizophrenia (6A20)
* Schizoaffective disorder (6A21)
* Schizotypal disorder (6A22)
* Acute and transient psychotic disorder (6A23)
* Delusional disorder (6A24)
* Other specified (6A2Y) or unspecified (6A2Z) primary psychotic disorder
* Bipolar type I disorder with psychotic symptoms (6A60.1, 6A60.5, 6A60.7, 6A60.A)
* Bipolar type II disorder with psychotic symptoms (6A61.3, 6A61.5)
* Single episode depressive disorder with psychotic symptoms (6A70.2, 6A70.4)
* Recurrent depressive disorder with psychotic symptoms (6A71.2, 6A71.4)
* Mental or behavioural disorder associated with pregnancy, childbirth or the puerperium, with psychotic symptoms (6E21)

Exclusion Criteria:

* People who are currently homeless, for logistical reasons; the SUCCEED intervention relies on PSWs and CSWs being able to regularly contact participants, including for home visits.
* People with secondary psychotic syndromes (6E61), as these are considered to be the direct consequences of physical health conditions as opposed to mental health conditions.
* People diagnosed with a substance-induced psychotic disorder (6C40.6-6C47.6), as recovery from substance use conditions is a specialist area outside the scope of the SUCCEED intervention under development.

Where it's running

  • University of Makeni
    Makeni, Northen Province, Sierra Leone
    Recruiting
  • University of Zimbabwe
    Harare, North East, Zimbabwe
    Recruiting
  • Kamuzu University of Health Sciences
    Blantyre, Southern, Malawi
    Not yet recruiting
  • University of Ibadan
    Ibadan, Oyo State, Nigeria
    Not yet recruiting

Study contacts

  • Principal investigator: Professor Thomas Shakespeare — London School of Hygiene and Tropical Medicine
  • Study coordinator: Dr Julian Eaton
  • Email: julian.eaton@lshtm.ac.uk
  • Phone: +44 77 11140365

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.