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Can a smartphone app and video therapy help young people with HIV?
NCT ID NCT05877729
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a combination of weekly video-counseling sessions and a mobile app can help young adults (18-29) living with HIV achieve viral suppression. Participants who are not virally suppressed will be randomly assigned to receive the intervention or standard care. The program aims to address barriers like medication forgetfulness, mental health issues, and substance use. The trial will compare viral suppression rates and mental health outcomes after 16 weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- video-counseling plus mobile health app
- What this could lead to
- If successful, this could provide an effective, scalable way to help young people with HIV achieve viral suppression and improve mental health and substance use outcomes.
- What could go wrong
- This is a relatively small, early-stage trial (200 participants) testing a behavioral intervention, not a drug. Results may not generalize to all populations, and the intervention requires active participation, which may limit real-world impact.
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 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2023
- Expected to finish
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Dec 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 to 29 years
- 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: 1. 18-29 years of age 2. HIV seropositive 3. Live and receive HIV care in California or Florida 4. Diagnosed with HIV more than 3 months ago 5. HIV VL test result of ≥20 copies at some point in the last 12 months (excluding tests within 3 mo of diagnosis) 6. Able to speak English 7. Have access to smartphone Exclusion Criteria: 1. Unable or unwilling to provide consent. 2. Evidence of severe cognitive impairment, active psychosis, or substance use that may impede ability to provide informed consent during the consent process. 3. Those with a history of hemophilia or unable to conduct finger prick at home for the HIV viral load testing.
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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.
Contacts and locations
Locations
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Division of Prevention Science, Center for AIDS Prevention Studies (CAPS)
San Francisco, California, 94143, United States
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Other studies related to the condition(s) this trial covers.
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