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Supporting Attendance for Facility Delivery and Infant Health — SAFI  

HIV Clinical Trial

Official title:
Enhancing Retention in PMTCT/MNCH Services and Facility Delivery in Tabora, Tanzania

Clinical Trial Summary

The goal of this proposed intervention study is to increase the proportion of HIV positive and HIV negative pregnant women who deliver in a facility, the proportion of HIV exposed infants (HEI) who receive nevirapine (NVP) within 48 hours of delivery, and the proportion of HEI who are bled for HIV polymerase chain reaction (PCR) deoxyribonucleic acid (DNA) testing within 8 weeks of age.

Clinical Trial Description

Following a formative phase I, we propose in phase II to implement a three-group cluster-randomized study to test the effectiveness of short message service (SMS) reminders and notifications, [mobile health or mhealth] (group 1) and the combined effectiveness of SMS reminders/notifications and cash transfers (group 2) compared to the standard prevention of mother-to-child transmission (of HIV)/maternal, neonatal and child health, (PMTCT/MNCH) practices (group 3). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03023033
Study type Interventional
Source Elizabeth Glaser Pediatric AIDS Foundation
Contact
Status Completed
Phase N/A
Start date October 2014
Completion date November 2016
View Details
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