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Mobile Phone Technology for Prevention of Mother-to-Child Transmission of HIV: Acceptability, Effectiveness, and Cost (Kenya)

Mobile Phone Technology for Prevention of Mother-to-Child Transmission of HIV: Acceptability, Effectiveness, and Cost (Kenya)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01645865
Enrollment
600
Registered
2012-07-20
Start date
2011-05-01
Completion date
2014-04-01
Last updated
2026-09-10

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

Conditions

AIDS, Antiretroviral Therapy, HIV, HIV Infections

Keywords

HIV, AIDS, PMTCT, Mobile Phone, SMS

Brief summary

Although gains have been made in achieving the health-related Millennium Development Goals (MDG), much is still needed in countries affected by high levels of HIV/AIDS. Prevention of mother-to-child transmission (PMTCT) is a cornerstone strategy in reducing infant mortality from HIV. The study will employ a cluster randomized control trial (cRCT) with 26 health facilities randomized to two arms (intervention or control) to determine the effect of mobile phone technology on completion of key PMTCT milestones from antenatal to six weeks postpartum. The study will examine the acceptability, effectiveness, and cost of implementing a PMTCT-focused mHealth strategy among HIV-infected pregnant women, health workers, and male partners.

Interventions

BEHAVIORALControl

Health facilities where PMTCT services are available in the traditional clinical setting with HIV testing and counseling, PMTCT support, and enrollment in care and treatment.

BEHAVIORALIntervention

In addition to the 'Standard of Care', HIV-infected pregnant women and male partners within the PMTCT program are engaged in multi-directional mobile communication for PMTCT promotion with health care providers.

Sponsors

Elizabeth Glaser Pediatric AIDS Foundation
Lead SponsorOTHER
World Health Organization, Alliance for Health Policy and Systems Research
CollaboratorUNKNOWN
Kenya National AIDS & STI Control Programme
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

(female): * HIV-positive pregnant women seeking ANC at a study site * Up to 32 weeks gestation * Own or have access to a mobile phone on which they can receive calls and SMS messages

Exclusion criteria

(female): * HIV-positive pregnant women who have already initiated antiretroviral treatment Inclusion Criteria (male): * Referral by pregnant female partner

Design outcomes

Primary

MeasureTime frame
The proportion of women who successfully complete key PMTCT transition points from antenatal to six weeks postpartum.~ 6 months
Initiation of Infant prophylaxis, Facility delivery and receipt of results of 6 weeks early infant diagnosis by DNA PCR~ 6 months

Secondary

MeasureTime frame
Uptake ARV prophylaxis/ART during labor, delivery, and postpartum~ 6 months
Self-reported maternal adherence to ARV prophylaxis/ART during pregnancy~ 4 months
Time to initiation of ARV prophylaxis/ART uptake after initial identification of HIV seropositivity within ANC~ 1 month

Countries

Kenya

Contacts

PRINCIPAL_INVESTIGATORJohn Ong'ech, MBChB, MMed, MPH

Elizabeth Glaser Pediatric AIDS Foundation, UON/KNH

PRINCIPAL_INVESTIGATORSeble Kassaye, MD, MS

Elizabeth Glaser Pediatric AIDS Foundation

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 11, 2026