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PrEP Implementation for Mothers in Antenatal Care

Delivering PrEP in Pregnancy

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03070600
Acronym
PrIMA
Enrollment
4447
Registered
2017-03-03
Start date
2018-01-15
Completion date
2021-01-15
Last updated
2022-07-12

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

Conditions

HIV Infections, Pregnancy Related

Keywords

PrEP

Brief summary

In a region with 15-20% HIV prevalence, an estimated 20% of HIV-uninfected women could have HIV exposures in pregnancy. In a theoretical scenario of perfect PrEP coverage, all women at risk receive PrEP while no women not at HIV risk receive PrEP (Figure 4). With mandatory PrEP given to all women (similar to the approaches used for malaria prophylaxis), all women at risk would be covered but many women not at risk receive unnecessary PrEP. Our premise is that a targeted PrEP model may be closer to perfect coverage than a universal offer/self-select model. Implementing targeted PrEP through strategies that include facilitation of partner testing with self-tests could add HIV prevention benefit by increasing partner HIV diagnosis and treatment similar to the initiation of PrEP among pregnant women. By implementing these strategies and measuring uptake, use, and HIV incidence, we can inform the best health systems model for PrEP delivery in pregnancy.

Detailed description

Women living in regions with high HIV prevalence are at high risk of HIV acquisition in pregnancy and postpartum because they infrequently use condoms, do not know their partner's HIV status, and have biologic changes or changes in their partner's sexual partnerships that increase susceptibility. Oral pre-exposure antiretroviral prophylaxis (PrEP) may be an attractive strategy for HIV prevention in pregnancy/postpartum; however, it is important to ensure PrEP reaches women who are at risk for acquiring HIV during pregnancy while avoiding unnecessary PrEP use during pregnancy. Clinicians and women are using PrEP in pregnancy; in qualitative studies, women, health workers and policy-makers support use of PrEP in pregnancy but advocate for models of PrEP delivery that ensure women at risk receive PrEP while minimizing unnecessary PrEP use in women not at risk. Targeting PrEP to women at greatest risk of HIV may maximize benefits, minimize potential risks, and optimize cost-effectiveness. This cluster-randomized clinical trial (RCT) in 20 Maternal Child Health (MCH) clinics in western Kenya (10 clinics per arm, up to 250 women per clinic, up to 5000 women overall), will compare 2 models of PrEP delivery in pregnancy. Clinics will offer universal availability of PrEP (and women self-select whether to use) or targeted offer of PrEP (i.e., offer to women identified as high risk through a standardized risk assessment and partner self-testing, and then women identified as high-risk select whether to use). Leveraging the pre-existing MCH clinic visit schedule will enable programmatically relevant assessment of PrEP uptake, use, and HIV incidence. The outcome of the study will be a model of PrEP delivery in pregnancy that optimizes effectiveness, safety, and cost-effectiveness. Our team has expertise in maternal-child HIV (John-Stewart, Kinuthia), PrEP clinical trials and implementation science (Baeten, Richardson), partner self-testing (Thirumurthy), economics and qualitative research (Barnabas, O'Malley). AIM 1a. In a cluster-RCT, compare universal PrEP (offer to all; women self-select PrEP) to targeted PrEP (limit the offer to women identified as high risk through a standardized risk assessment and partner self-testing) for outcomes reflecting the balance of PrEP effectiveness and avoiding unnecessary PrEP exposure to women at low or no risk of HIV: HIV incidence at 9 months postpartum among all women (including those who did and did not receive PrEP) and proportion of women exposed to PrEP. AIM 1b. To compare trial arms for proportion of women 'appropriately' on PrEP (risk factors), PrEP adherence (drug levels) and duration, partners with known HIV status, partners on ART; infant outcomes (growth, birth outcomes, HIV status). AIM 2. To estimate the incremental cost-effectiveness of targeted PrEP compared to universal PrEP for women during pregnancy and postpartum, per HIV infection and disability-adjusted life-year (DALY) averted. AIM 3. To qualitatively assess barriers and facilitators to uptake, adherence, acceptability, and feasibility in universal and targeted PrEP models at the organizational, provider, and individual woman level.

Interventions

OTHERUniversal PrEP Counseling

Counseling at universal sites, will use a standardized counseling script to state that PrEP is available for women at risk for HIV, explain that HIV prevalence in the region is high, and will note that women with HIV positive partners or who don't know their partner's status may be at risk. Counseling will specify that women may have their own reasons to feel at risk or to want PrEP. Following standardized counseling, women will select PrEP at the same visit or will be allowed to deliberate on the decision and come back at the next visit with a decision. Women will be informed that it is advisable to use PrEP if they know their partner is HIV positive or if they do not know their partner's status and will be encouraged to bring untested partners to clinic if status is unknown.

OTHERTargeted PrEP Counseling

Following enrollment, the targeted PrEP clinics will provide two inter-related innovations over two ANC visits. In the targeted PrEP clinics, any of the following three criteria can trigger enhanced PrEP counseling. A participant that meets any one of these criteria will receive PrEP counseling during the study visit where the criteria is met: 1. Risk Score \>6 (Risk score includes male partner status known/unknown, syphilis infection, and lifetime number of male partners) or any National AIDS and STI Control Programme (NASCOP) risk factors 2. participant declines partner self-tests regardless of partner HIV status, and/or 3. their partner declines self-testing or tests positive.

Sponsors

Kenyatta National Hospital
CollaboratorOTHER_GOV
National Institute of Allergy and Infectious Diseases (NIAID)
CollaboratorNIH
University of Washington
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

We will select 20 clinics from Western Kenya. Ten clinics will be randomized to universal PrEP and ten to targeted PrEP (Table 2). To ensure balance between study arms in terms of key site characteristics, sites will be categorized on HIV prevalence and ANC volume, and restricted randomization will be used for site (cluster) allocation to intervention and control arms (68).

Eligibility

Sex/Gender
FEMALE
Age
15 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Eligibility for enrollment will include age ≥15 years * Pregnant at any gestational age * Tuberculosis negative * Plans to reside in area for at least one year postpartum * Plans to receive postnatal and infant care at the study facility * Not currently enrolled in any other studies.

Exclusion criteria

* HIV+ at time of enrollment

Design outcomes

Primary

MeasureTime frameDescription
Maternal HIV Incidence6 weeks, 6 months, 9 months postpartumMaternal HIV Incidence
Appropriate PrEP DecisionEnrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).Scored 1 for high risk women using PrEP and low risk women not using PrEP; 0 for high risk women NOT on PrEP and low risk women using PrEP

Secondary

MeasureTime frameDescription
PrEP DurationEnrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).Number of months on PrEP
Partner With Known HIV StatusAt 9 months postpartumParticipants report of partner's HIV status
Infant Birthweighttime of deliveryInfant Birthweight
PrEP UseEnrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).PrEP Utilization by participants
PrEP AcceptanceEnrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).PrEP accepted by participants
Preterm BirthAt birthBirth \<37 weeks gestation
Infant Growth9 months of ageInfant height, weight, and age (Weight-for-Age \[WAZ\], Height-for-Age \[HAZ\], Weight-for-Height \[WHZ\] Z-scores). A Z-score of 0 represents the population mean. Indicators of infant malnutrition are defined as Underweight- WAZ Z-score\<-2; Stunting-HAZ Z-Score \<-2; Wasting- WHZ Z-Score \<-2.
PrEP AdherenceEnrollment to 9 months postpartumSequential dried blood spots, PrEP adherence by DBS dichotomous by pregnancy or postpartum thresholds equivalent to \ 7 doses per week (≥650 fmol/punch during pregnancy or ≥950 fmol/punch postpartum) based on the thresholds established by the 2009 IMPAACT directly observed PrEP PK study.

Other

MeasureTime frameDescription
PrEP Adherence by Self-reportEnrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).Any missed doses in the last month reported by participants
Partner on ART if HIV PositiveEnrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).Participant report of partner ART use if partner is HIV positive

Countries

Kenya

Participant flow

Pre-assignment details

Enrollment ended on July 31, 2019. At that time 4,447 women had enrolled (consented) into the PrIMA study out of an anticipated 4,500.

Participants by arm

ArmCount
Universal PrEP Counselling
All enrolled women receiving antenatal care at facilities assigned to Universal PrEP arm will receive standardized HIV risk counseling and then self-select whether they want to use PrEP. Universal PrEP Counseling: Counseling at universal sites, will use a standardized counseling script to state that PrEP is available for women at risk for HIV, explain that HIV prevalence in the region is high, and will note that women with HIV positive partners or who don't know their partner's status may be at risk. Counseling will specify that women may have their own reasons to feel at risk or to want PrEP. Following standardized counseling, women will select PrEP at the same visit or will be allowed to deliberate on the decision and come back at the next visit with a decision. Women will be informed that it is advisable to use PrEP if they know their partner is HIV positive or if they do not know their partner's status and will be encouraged to bring untested partners to clinic if status is unknown.
2,250
Targeted PrEP Clinics
All enrolled women receiving antenatal care at facilities assigned to the Targeted PrEP arm will be assessed for HIV-risk prior to receiving targeted PrEP counseling. Targeted PrEP Counseling: Following enrollment, the targeted PrEP clinics will provide two inter-related innovations over two ANC visits. In the targeted PrEP clinics, any of the following three criteria can trigger enhanced PrEP counseling. A participant that meets any one of these criteria will receive PrEP counseling during the study visit where the criteria is met: 1. Risk Score \>6 (Risk score includes male partner status known/unknown, syphilis infection, and lifetime number of male partners) or any National AIDS and STI Control Programme (NASCOP) risk factors 2. participant declines partner self-tests regardless of partner HIV status, and/or 3. their partner declines self-testing or tests positive.
2,197
Total4,447

Baseline characteristics

CharacteristicTargeted PrEP ClinicsUniversal PrEP CounsellingTotal
Age, Continuous24.1 years23.9 years24.0 years
Age, Customized
25-35
850 Participants830 Participants1680 Participants
Age, Customized
<25 years of age
1238 Participants1307 Participants2545 Participants
Age, Customized
35+
108 Participants112 Participants220 Participants
Age, Customized
Age missing
1 Participants1 Participants2 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
2197 Participants2250 Participants4447 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
0 Participants0 Participants0 Participants
Region of Enrollment
Kenya
2197 participants2250 participants4447 participants
Sex: Female, Male
Female
2197 Participants2250 Participants4447 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
2 / 2,2502 / 2,197
other
Total, other adverse events
7 / 2,2507 / 2,197
serious
Total, serious adverse events
132 / 2,250118 / 2,197

Outcome results

Primary

Appropriate PrEP Decision

Scored 1 for high risk women using PrEP and low risk women not using PrEP; 0 for high risk women NOT on PrEP and low risk women using PrEP

Time frame: Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Universal PrEP CounsellingAppropriate PrEP Decision1535 Participants
Targeted PrEP ClinicsAppropriate PrEP Decision1299 Participants
Primary

Maternal HIV Incidence

Maternal HIV Incidence

Time frame: 6 weeks, 6 months, 9 months postpartum

ArmMeasureValue (NUMBER)
Universal PrEP CounsellingMaternal HIV Incidence0.38 incidence/100 Person years
Targeted PrEP ClinicsMaternal HIV Incidence0.31 incidence/100 Person years
Secondary

Infant Birthweight

Infant Birthweight

Time frame: time of delivery

Population: This analysis is restricted to mothers with live born infants with birth weight data available in their clinical records.

ArmMeasureValue (MEDIAN)
Universal PrEP CounsellingInfant Birthweight3.5 kg
Targeted PrEP ClinicsInfant Birthweight3.5 kg
Secondary

Infant Growth

Infant height, weight, and age (Weight-for-Age \[WAZ\], Height-for-Age \[HAZ\], Weight-for-Height \[WHZ\] Z-scores). A Z-score of 0 represents the population mean. Indicators of infant malnutrition are defined as Underweight- WAZ Z-score\<-2; Stunting-HAZ Z-Score \<-2; Wasting- WHZ Z-Score \<-2.

Time frame: 9 months of age

Population: Length measurements could not be ascertained from all infants

ArmMeasureGroupValue (MEDIAN)
Universal PrEP CounsellingInfant GrowthInfant WAZ at 9mo PP0.12 z-score
Universal PrEP CounsellingInfant GrowthInfant HAZ at 9mo PP-0.35 z-score
Universal PrEP CounsellingInfant GrowthInfant WHZ at 9mo PP0.42 z-score
Targeted PrEP ClinicsInfant GrowthInfant WAZ at 9mo PP-0.01 z-score
Targeted PrEP ClinicsInfant GrowthInfant HAZ at 9mo PP-0.47 z-score
Targeted PrEP ClinicsInfant GrowthInfant WHZ at 9mo PP0.29 z-score
Secondary

Partner With Known HIV Status

Participants report of partner's HIV status

Time frame: At 9 months postpartum

Population: This analysis is restricted to participants who reported having a partner at 9-months postpartum.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Universal PrEP CounsellingPartner With Known HIV Status1680 Participants
Targeted PrEP ClinicsPartner With Known HIV Status1648 Participants
Secondary

PrEP Acceptance

PrEP accepted by participants

Time frame: Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Universal PrEP CounsellingPrEP Acceptance441 Participants
Targeted PrEP ClinicsPrEP Acceptance387 Participants
Secondary

PrEP Adherence

Sequential dried blood spots, PrEP adherence by DBS dichotomous by pregnancy or postpartum thresholds equivalent to \ 7 doses per week (≥650 fmol/punch during pregnancy or ≥950 fmol/punch postpartum) based on the thresholds established by the 2009 IMPAACT directly observed PrEP PK study.

Time frame: Enrollment to 9 months postpartum

Population: Of the 186 participants sampled for this analyses, 427 DBS samples were analyzed (232 universal arm, 195 targeted arm).

ArmMeasureValue (NUMBER)
Universal PrEP CounsellingPrEP Adherence7 Samples w/ adherence at ~7dose/week
Targeted PrEP ClinicsPrEP Adherence9 Samples w/ adherence at ~7dose/week
Secondary

PrEP Duration

Number of months on PrEP

Time frame: Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).

Population: This analysis is restricted to participants who initiated PrEP during the study period.

ArmMeasureValue (MEDIAN)
Universal PrEP CounsellingPrEP Duration8.6 months
Targeted PrEP ClinicsPrEP Duration9.0 months
Secondary

PrEP Use

PrEP Utilization by participants

Time frame: Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Universal PrEP CounsellingPrEP Use397 Participants
Targeted PrEP ClinicsPrEP Use323 Participants
Secondary

Preterm Birth

Birth \<37 weeks gestation

Time frame: At birth

Population: This analysis is restricted to participants who reported a live birth and had gestational age at birth data available.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Universal PrEP CounsellingPreterm Birth506 Participants
Targeted PrEP ClinicsPreterm Birth309 Participants
Other Pre-specified

Partner on ART if HIV Positive

Participant report of partner ART use if partner is HIV positive

Time frame: Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).

Population: This analysis is restricted to participants with a partner known to be living with HIV.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Universal PrEP CounsellingPartner on ART if HIV Positive37 Participants
Targeted PrEP ClinicsPartner on ART if HIV Positive31 Participants
Other Pre-specified

PrEP Adherence by Self-report

Any missed doses in the last month reported by participants

Time frame: Enrollment to 9 months postpartum, the median gestational age at enrollment was 24 weeks (IQR: 20, 30).

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Universal PrEP CounsellingPrEP Adherence by Self-report184 Participants
Targeted PrEP ClinicsPrEP Adherence by Self-report120 Participants

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026