Phone-Based program aims to boost mental health screening in uganda
NCT ID NCT07525271
First seen Jun 27, 2026 · Last updated Aug 20, 2026 · Updated 4 times
Summary
This study tests a mobile health program called SAMU to help adults in Uganda who have HIV, high blood pressure, and mental health issues like depression or anxiety. About 1,500 participants will use their phones for mental health screening and get connected to care. The goal is to see if the program improves diagnosis and treatment for these overlapping health problems.
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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 1,500 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2028
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.
Inclusion Criteria: * Patient at a participating HIV clinic site * Currently living in Uganda with no intention of moving abroad in next 2 years * Access to a mobile phone * Basic reading skills in one or more of the offered languages (English, Luganda) as determined by the Research Assistant. Exclusion Criteria: * No access to a mobile phone * Inability to provide informed consent based on assessment by the onsite Research Assistant or HCW Healthcare Workers/Caregivers Criteria: * Age \>=18 years * Healthcare worker at participating site or caregiver for study participant at site * Basic reading skills in one or more of the offered languages (English, Luganda) as determined by the Research Assistant
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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
3 sites. 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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Kawaala Hospital
Kampala, Uganda
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Naguru Hospital
Kampala, Uganda
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Nsambya Hospital
Kampala, Uganda
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