ClinicalTrials.Veeva

Menu

Antiretroviral Adherence Evaluation in HIV Pregnant and Postpartum Women

U

University Center for Primary Care and Public Health (Unisanté)

Status

Completed

Conditions

HIV Infection
Pregnancy

Study type

Observational

Funder types

Other
NETWORK

Identifiers

Details and patient eligibility

About

The purpose of this study is to compare adherence to antiretroviral therapy during pregnancy and postpartum, and to record adherence barriers and facilitators.

Full description

Data of all consecutive pregnant women included in the adherence enhancing program of the Pharmacy, Department of ambulatory care & community medicine, are collected. In this program, adherence is measured and enhanced by electronic monitoring, pill count, motivational interviewing and interdisciplinary collaboration. Electronic monitoring data are collected during pregnancy and postpartum, and compared. Barriers and facilitators are collected using interview's marks.

Enrollment

26 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Pregnant Women
  • HIV-positive
  • Antiretroviral medication delivered in electronical monitors

Exclusion criteria

  • Monitored period during pregnancy < 1 month

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems