Effect of an interactive SMS system in improving the reporting of adverse drug reactions among people living with HIV in Tanzania and Uganda: a randomized controlled trial: The REMIND ADR TRIAL

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR202503561138751

Enrollment

228

Registered

2025-03-03

Start date

2023-08-01

Completion date

Unknown

Last updated

2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV/AIDS

Interventions

SMS reminders

Standard of care

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: ? Age between 18 and 65 ? confirmed and documented HIV infection ? Being on ART treatment for at least 3 months ? Able to read and understand SMS ? Able to understand and be willing to sign the informed consent document ? Able to read and write a text message ? Have a mobile phone

Exclusion criteria

Exclusion criteria: ? Critically ill patients. ? Participating in other clinical trials.

Design outcomes

Primary

Measure	Time frame
The main outcome measure will be the proportion of participants reporting ADR in the two arms.	—

Secondary

Measure	Time frame
The other outcome measures will be the frequencies of the different ADR profiles reported	—

Countries

Tanzania, Uganda, United Republic of Tanzania

Contacts

Public ContactKenedy;Benjamin Ngowi;Watyaba

Researcher at KCRI;Reseacher

k.ngowi@kcri.ac.tz;bwatyaba@uvri.go.ug+255758048649;+256777601103

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026