New study aims to keep mentally ill patients out of the hospital
NCT ID NCT07339462
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a support program for people with severe mental illness after they leave the hospital in South Africa. The program includes better referral pathways and psychosocial support for patients and their caregivers. Researchers will see if it reduces the number of people who need to be readmitted within four months. The study involves 86 adults recently hospitalized for conditions like schizophrenia or severe mood disorders.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Multilevel psychosocial support program
- What this could lead to
- If successful, this could point toward a practical way to reduce hospital readmissions for people with severe mental illness in low-resource settings.
- What could go wrong
- This is a small, early feasibility study with only 86 participants, so results may not apply broadly. The intervention is complex and may be hard to implement consistently.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 86 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2025
- Expected to finish
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Aug 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Service user inclusion criteria: * Adults (aged 18 years and above); * Being admitted to the psychiatric ward of a hospital for observation and treatment due to an acute psychiatric event, based on ICD diagnosis on patient charts according to the following criteria: * F20-29 including schizophrenia, delusional disorders, schizotypal disorders, acute polymorph psychotic disorders, schizoaffective disorders * F30-39 Mood \[affective\] disorders with psychoses * F30.2 Mania with psychotic symptoms * F31.2 Bipolar affective disorder, current episode manic with psychotic symptoms * F31.5 Bipolar affective disorder, current episode severe depression with psychotic symptoms * F32.3 Severe depressive episode with psychotic symptoms * F33.3 Recurrent depressive disorder, current episode severe with psychotic symptoms * Determined by the attending psychiatrist to be discharged into community settings following appropriate recovery from the psychiatric event; * Willing and able to participate in the intervention programme * Resides with a caregiver (which could be a family member or member of the household). * Resides within the geographic boundaries of uMgungundlovu Service user exclusion criteria: * Under 18 years of age * Are indicated by their chart history to have the following conditions: * Active suicidal ideation * Substance abuse or dependence as primary diagnosed psychiatric condition * Personality disorders * Serious cognitive or other sensorial impairment likely to preclude informed consent and reliable assessment * Does not reside with a caregiver * Does not reside within the geographic boundaries of uMgungundlovu Caregiver inclusion criteria * Adults (aged 18 years and above) * Willing and able to participate in the intervention programme * Resides with a caregiver (which could be a family member or member of the household). * Resides within the geographic boundaries of uMgungundlovu Caregiver exclusion criteria * Adults (aged 18 years and above) * Willing and able to participate in the intervention programme * Resides with a caregiver (which could be a family member or member of the household). * Resides within the geographic boundaries of uMgungundlovu
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Msunduzi Local Municipality
RECRUITINGPietermaritzburg, KwaZulu-Natal, 3201, South Africa
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Other studies related to the condition(s) this trial covers.
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