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PrEPARE: PrEP in Pregnancy, Accelerating Reach and Efficiency

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University of Washington

Status

Completed

Conditions

Pre-Exposure Prophylaxis
Pregnancy Related
HIV Infections

Treatments

Other: PrEP Optimization Interventions

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04712994
R01HD094630 (U.S. NIH Grant/Contract)
R01AI125498 (U.S. NIH Grant/Contract)
STUDY00008392

Details and patient eligibility

About

This study tests strategies for improving PrEP implementation in maternal and child health clinics using a difference-in-difference approach.

Full description

This study aims to improve integrated delivery of PrEP to women seeking health services in maternal and child health clinics by piloting and evaluating four strategies or bundles of strategies for optimized PrEP delivery. Strategies to be tested include a pre-developed package of strategies (video counseling, HIV self-testing, and optimized delivery).

Enrollment

1,958 patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women receiving Maternal and Child Health (MCH) services HCW participating in satisfaction surveys

Exclusion criteria

  • Unwilling or unable to provide informed consent

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

1,958 participants in 2 patient groups

PrEP Optimization Strategies
Experimental group
Description:
Four facilities will be assigned to the intervention group. The intervention group will receive a pre-identified package of interventions (PrEP video counselling, HIV Self-Testing, and optimized delivery and prescription processes).
Treatment:
Other: PrEP Optimization Interventions
Comparator
No Intervention group
Description:
Four facilities will be assigned to the comparator group.

Trial documents
2

Trial contacts and locations

8

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Central trial contact

Julia Dettinger, MPH; Lauren Gomez, MPH

Data sourced from clinicaltrials.gov

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