Improving Uptake of Early Infant Diagnosis of HIV for the Prevention of Mother-to-child Transmission of HIV (SMS4PMTCT)
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Purpose
Early accurate diagnosis is one of the first crucial steps in care for infants born to HIV-infected mothers. Early initiation of antiretroviral therapy (ART) relies upon early diagnosis and results in significant reductions in infant morbidity and mortality. There is little information on evidence-based interventions that specifically target improved attendance of postpartum clinic visits and subsequent infant HIV testing in the context of prevention of mother-to-child transmission of HIV (PMTCT) programs. The investigators propose a randomized controlled trial to examine the effect of text messages sent to women enrolled in PMTCT programs on adherence to postpartum clinic visits and uptake of early infant diagnosis by DNA polymerase chain reaction (PCR). This study seeks to test the hypotheses that (a) text messages sent to women enrolled in PMTCT will improve their attendance at the postnatal clinic within the first 6-8 weeks after childbirth; and (b) text messages sent to women enrolled in PMTCT programs will increase uptake of DNA PCR HIV testing at 6-8 weeks among infants exposed to HIV. This study will evaluate a novel strategy to improve adherence to postnatal clinic visits and increase the uptake of infant HIV testing. If proven superior to standard care, the proposed intervention can be easily scaled-up and integrated into existing healthcare systems in resource-limited settings. Findings from this study will provide randomized trial evidence to inform HIV prevention program planners and implementers. This study will also provide further information on the feasibility of using mobile phone-based technology for public health interventions in resource-limited settings.
| Condition | Intervention |
|---|---|
|
HIV Infections Acquired Immunodeficiency Syndrome |
Other: Text message |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Supportive Care |
| Official Title: | Improving Uptake of Early Infant Diagnosis of HIV for PMTCT: a Randomized Trial of a Text Messaging Intervention |
- Proportion of women who attend postnatal clinic within 6-8 weeks postpartum [ Time Frame: 6-8 weeks after delivery ] [ Designated as safety issue: No ]
- Proportion of infants tested for HIV by DNA PCR [ Time Frame: 6-8 weeks after delivery ] [ Designated as safety issue: No ]
- Infant adherence to antiretroviral prophylaxis [ Time Frame: Up to 6 weeks after delivery ] [ Designated as safety issue: No ]
- Time to post-natal clinic return [ Time Frame: Up to 8 weeks after delivery ] [ Designated as safety issue: No ]
- Maternal adherence to antiretroviral prophylaxis [ Time Frame: Up to 8 weeks after delivery ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 448 |
| Study Start Date: | April 2012 |
| Estimated Study Completion Date: | December 2012 |
| Estimated Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Text message (SMS)
Text messages sent to women before and after delivery
|
Other: Text message
Text messages sent to women before and after delivery
Other Name: SMS, short message service, text messaging
|
|
No Intervention: Usual care (current standard of care)
Current standard of care for women enrolled in PMTCT programs
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- age at least 18 years
- report ability to read SMS
- ≥ 28 weeks gestation or delivery at study clinic on day of enrollment
- HIV positive women enrolled in the PMTCT program
- have access to a mobile phone (personal or partner's if HIV serostatus disclosed to partner)
- willing to receive SMS messages from the study
- planning to remain in the study area (Nyanza province) for the duration of the study
Exclusion Criteria:
- age less than 18 years old
- women who share phones with partners but HIV status not disclosed to partners
- intention to deliver at a non-study hospital
Contacts and Locations| Contact: Thomas A Odeny, MBChB, MPH | (057)2021036 | odeny@uw.edu |
| Contact: R S McClelland, MD, MPH | 206-473-0392 | mcclell@uw.edu |
| Kenya | |
| Kenya Medical Research Institute, Family AIDS Care and Education Services | Recruiting |
| Kisumu, Nyanza, Kenya | |
| Principal Investigator: Thomas A Odeny, MBChB, MPH | |
| Principal Investigator: | Thomas A Odeny, MBChB, MPH | University of Washington/Kenya Medical Research Institute |
| Study Chair: | R Scott McClelland, MD, MPH | University of Washington |
| Study Chair: | Craig R Cohen, MD, MPH | University of California, San Francisco |
| Study Chair: | Carol Camlin, PhD | University of California, San Francisco |
| Study Chair: | Elizabeth A Bukusi, MBChB, MMed, MPH, PhD | Kenya Medical Research Institute |
More Information
No publications provided
| Responsible Party: | Thomas Odeny, Principal Investigator, University of Washington |
| ClinicalTrials.gov Identifier: | NCT01433185 History of Changes |
| Other Study ID Numbers: | 41186-E/G |
| Study First Received: | September 12, 2011 |
| Last Updated: | September 11, 2012 |
| Health Authority: | United States: Institutional Review Board Kenya: Ethical Review Committee |
Keywords provided by University of Washington:
|
PMTCT SMS HIV Infections Acquired Immunodeficiency Syndrome |
Prevention & Control Patient Compliance Cellular Phone Randomized Controlled Trial |
Additional relevant MeSH terms:
|
Acquired Immunodeficiency Syndrome HIV Infections Immunologic Deficiency Syndromes Lentivirus Infections Retroviridae Infections RNA Virus Infections |
Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Slow Virus Diseases Immune System Diseases |
ClinicalTrials.gov processed this record on June 18, 2013