Adapting the HITSystem to Support Prevention of Mother-to-child HIV Transmission
Status: | Enrolling by invitation |
---|---|
Conditions: | HIV / AIDS |
Therapuetic Areas: | Immunology / Infectious Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 10/28/2018 |
Start Date: | August 2015 |
End Date: | April 2019 |
The purpose of this study is to modify the HITSystem to engage and retain HIV+ pregnant women
before, during and after delivery and evaluate the HITSystem impact on prevention of
mother-to-child transmission (PMTCT) related behaviors and outcomes. HITSystem 2.0
intervention will support a range of PMTCT outcomes including retention in care, ART
adherence, and integration of maternal and pediatric HIV services in low-resource settings.
before, during and after delivery and evaluate the HITSystem impact on prevention of
mother-to-child transmission (PMTCT) related behaviors and outcomes. HITSystem 2.0
intervention will support a range of PMTCT outcomes including retention in care, ART
adherence, and integration of maternal and pediatric HIV services in low-resource settings.
The study will be conducted in three phases:
Phases 1: The researchers will conduct formative research (focus groups and interviews) with
HIV+ pregnant women and PMTCT providers to customize communication strategies for text
messaging and inform patient flow and optimal implementation across the various PMTCT-related
services at the intervention site.
Phase 2: The researchers will design and refine the HITSystem 2.0 technical components to
support PMTCT outcomes guided by clinical content experts, technology analysts, and findings
from Phase 1.
Phase 3: The researchers will implement HITSystem 2.0 at one hospital over an 18 month
period, and compare targeted PMTCT outcomes to those at a matched control hospital.
The study will be conducted at two government hospitals in Kenya. HIV+ pregnant women will be
enrolled in the HITSystem 2.0 at Kapsabet Hospital. HIV+ pregnant women receiving the current
standard of PMTCT care at Nandi Hills Hospital will be the comparison group.
Phases 1: The researchers will conduct formative research (focus groups and interviews) with
HIV+ pregnant women and PMTCT providers to customize communication strategies for text
messaging and inform patient flow and optimal implementation across the various PMTCT-related
services at the intervention site.
Phase 2: The researchers will design and refine the HITSystem 2.0 technical components to
support PMTCT outcomes guided by clinical content experts, technology analysts, and findings
from Phase 1.
Phase 3: The researchers will implement HITSystem 2.0 at one hospital over an 18 month
period, and compare targeted PMTCT outcomes to those at a matched control hospital.
The study will be conducted at two government hospitals in Kenya. HIV+ pregnant women will be
enrolled in the HITSystem 2.0 at Kapsabet Hospital. HIV+ pregnant women receiving the current
standard of PMTCT care at Nandi Hills Hospital will be the comparison group.
Phase 3
Inclusion Criteria:
- HIV+ pregnant women
- Present for first PMTCT appointment at one of the study Hospitals
- Own or have reliable access to mobile phone
Exclusion Criteria:
We found this trial at
2
sites
University of Kansas Medical Center The University of Kansas Medical Center serves Kansas through excellence...
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