Safer Conception for Women - Understanding Use of Periconception PrEP
Study Details
Study Description
Brief Summary
Women who choose to conceive with an infected or unknown serostatus partner in HIV-endemic settings need prevention strategies to reduce periconception HIV acquisition risk. Women at high risk for acquiring HIV during pregnancy need risk reduction strategies to protect themselves and their babies. Evaluating uptake of and adherence to antiretrovirals as pre-exposure prophylaxis in this population is crucial to understanding whether and how this novel prevention strategy should be incorporated into HIV-risk reduction packages for at- risk women planning or with pregnancy.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 4 |
Detailed Description
In HIV-endemic settings, many HIV-uninfected women choose to conceive with an HIV-infected or unknown-serostatus partner. For a woman who cannot depend on a partner to test, initiate and adhere to ART, sex without condoms puts her at high risk of acquiring HIV and increases the risk of perinatal transmission to her child. Daily, oral TDF/FTC PrEP dramatically reduces a woman's risk of HIV-acquisition and is the only female-controlled option for reducing the risk of periconception HIV-acquisition. Understanding whether daily, oral PrEP is feasible for uninfected women seeking pregnancy is critical to reducing HIV incidence among women and their children.
Placebo-controlled trials identified adherence as a major challenge to long-term PrEP use. However, women are eager for prevention strategies that allow for conception, and we hypothesize that adherence to a proven prevention strategy, for a limited time with the motivation to have a healthy child, will confer drug levels required to prevent HIV transmission. This project will inform whether daily, oral PrEP is a feasible HIV-prevention strategy for South African women who intend to conceive with risky partners. Given the repercussions of acquiring HIV during conception and pregnancy, this is an important step towards providing a key prevention strategy to women and their children.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Other: HIV-uninfected women A sample of 350 HIV-uninfected women who are not currently pregnant, in a stable relationship (≥6 months) with a self-reported infected or unknown serostatus partner and personal or partner plans for pregnancy in the next 12 months. Women will be offered safer conception counseling based on South African guidelines plus daily, oral tenofovir/emtricitabine (TDF/FTC) as pre-exposure prophylaxis (PrEP) during periconception and pregnancy. |
Behavioral: PrEP for Safer Conception
Evaluation of uptake of and adherence to PrEP and safer conception strategies including: CHCT, ART for the infected partner, and uptake of contraception for those who decide not to conceive by enrolled women, during periconception and pregnancy follow up.
|
Outcome Measures
Primary Outcome Measures
- Evaluation of uptake of and adherence to PrEP [minimum of 12 months through pregnancy outcome (maximum 21 months)]
The primary objective will be the evaluation of uptake of (collection of one month's supply) and adherence to PrEP (measured by quarterly plasma tenofovir levels) by women, during periconception and pregnancy follow up.
Secondary Outcome Measures
- Safer Conception Strategies [minimum of 12 months through pregnancy outcome (maximum 21 months)]
Secondary outcomes include uptake of safer conception strategies including CHCT, ART for the infected partner, uptake of contraception for those who decide not to conceive; HIV transmission events, infant outcomes, and findings from qualitative interviews to further inform the conceptual framework for periconception PrEP uptake and adherence.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Female, Aged 18-35 years
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Not pregnant, HIV-uninfected
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Likely to be fertile based on responses to reproductive history assessment
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Not on a long-acting family planning method
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Likely to have a child in the next year, either by response to modified CDC Pregnancy Risk Assessment [2-5]), or meeting the other inclusion criteria.
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With a stable (>= 6 months) partner she reports as HIV-infected or HIV-serostatus unknown, (if >1 desired pregnancy partner, we will ask her to identify the most likely pregnancy partner- based on her own assessment of sexual frequency, fertility, etc.)
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Able to participate in the informed consent process
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Fluent in English or isiZulu
Exclusion Criteria:
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Living at or planning to relocate to a location incompatible with study participation in the next year
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Active drug or alcohol use that, in the opinion of the research study team, would interfere with adherence to study requirements
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Active illness requiring systemic treatment and/or hospitalization within 30 days prior to study entry that in the opinion of the research study team, might otherwise interfere with adherence to study requirements
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Inability to adhere to the study schedule and/or study procedures
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Enrolment in studies which may conflict with their participation in this proposed study.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Maternal, Adolescent, and Child Health Research Unit (MRU) | Durban | KwaZulu-Natal | South Africa | 4001 |
Sponsors and Collaborators
- Massachusetts General Hospital
- National Institutes of Health (NIH)
- University of Witwatersrand, South Africa
- National Institute of Mental Health (NIMH)
Investigators
- Principal Investigator: Lynn T Matthews, MD, MPH, Mass General Hosptial
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2016P001535
- 1R01MH108412