A pharmacist's touch: could structured medication reviews boost HIV treatment success?
NCT ID NCT07750834
First seen Aug 06, 2026 · Last updated Aug 11, 2026 · Updated 3 times
Summary
This trial tests whether a structured, pharmacist-led medication management program can help HIV patients at high risk of drug-related problems take their medications more consistently. Participants are randomly assigned to usual care, a basic program, or an enhanced program with extra support like pill organizers and home visits. The study tracks adherence, viral load, and quality of life over 24 months to see if the extra support makes a meaningful difference.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Pharmacist-led Medication Therapy Management (MTM) program
- What this could lead to
- If effective, this program could become a standard approach to help HIV patients stick to their medications, potentially improving viral suppression and quality of life in resource-limited settings.
- What could go wrong
- The trial is early and the outcome depends on patient engagement and healthcare infrastructure. Results may not generalize beyond this specific setting, and the added pharmacist time may not prove cost-effective.
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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1,149 people
The number who actually took part.
- Started
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Jan 2021
- Finished
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Apr 2026
- 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 * Age: ≥18 years at the time of enrollment. * HIV Status: Laboratory-confirmed HIV infection. * ART Duration: Receiving antiretroviral therapy (ART) for at least 3 months prior to enrollment. --Language and Consent: Able to communicate in Arabic or English and willing and able to provide written informed consent. * High-Risk Status: Meeting at least 2 of the following high-risk criteria: * Receiving ≥8 chronic medications, including ART and medications for comorbidities. * Having ≥3 chronic comorbidities (e.g., diabetes mellitus, hypertension, hepatitis, or tuberculosis). * Documented or self-reported adverse drug event within the previous 12 months. * Viral load \>200 copies/mL during the previous 6 months. --Self-reported medication adherence \<95% or repeated missed clinic appointments. * Attendance at the participating HIV clinic on at least 2 occasions during the assessment period. Exclusion Criteria: * Age \<18 years. * Pregnancy. * Significant cognitive impairment preventing informed consent or study participation. * Terminal illness with expected life expectancy \<12 months. * Concurrent participation in another pharmacological intervention study. * Previous participation in a formal Medication Therapy Management (MTM) program within the past year. * Planned relocation away from Khartoum State during the follow-up period. * Inability to provide informed consent for any reason.
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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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Omdurman teaching Hospital
Khartoum, Omdurman, 1111, Sudan
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