Efficacy of SMS to Improve Early Retention in HIV Care for PLWH in Lima
- Conditions
- HIV
- Interventions
- Behavioral: Tailored text messages to improve retention in HIV care
- Registration Number
- NCT03862196
- Lead Sponsor
- NGO Via Libre
- Brief Summary
Randomized controlled study that will evaluate the effect of a text message-based strategy to improve retention in HIV care.
- Detailed Description
This is a randomized controlled pilot study with a parallel 2-arm design. It will evaluate the effect of a text message-based strategy to improve retention in HIV care at the study clinic, compared to the standard of care. Trained counselors will deliver the text messages. After a block randomization, the trained counselor (a nurse) will send the first welcoming message to participants in the intervention arm. The nurse will send 2 tailored text messages per week. In addition 2 to 4 days before an appointment, the nurse will send a message reminder. In addition, the nurse will have bilateral communication with participants using text messages according to their needs. The participants of the intervention arm will interact with the nurse during 3 months with a semi-structured strategy, that is, with template text messages (predesigned) and open messages (for which the nurse will be trained). Three and six months after started the intervention the variables of interest will be assessed.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- Male
- Target Recruitment
- 144
- Male 18 years old or older.
- Linked to HIV care at the study clinic.
- Have a cell phone.
- Diagnosed at the study clinic of referred from other center to start ART.
- Give consent to participate.
- Enrolled in other HIV study using text messages.
- Have started ART.
- Enrolled in a clinical trial.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intervention Tailored text messages to improve retention in HIV care Participants will receive 2 tailored text messages weekly from a trained counselor during 3 months.
- Primary Outcome Measures
Name Time Method Retention in timely monitoring of viral load (VL) 6 months Rate of participants with a second lab result of VL available 6 months after initiation of ART, verified using lab records
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Via Libre
🇵🇪Lima, Peru