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Evaluating Factors That Impact Loss to Follow-up Among Postpartum HIV-infected Women in Mississippi

Evaluating Factors That Impact Loss to Follow-up Among Postpartum HIV-infected Women in Mississippi

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01190605
Enrollment
53
Registered
2010-08-27
Start date
2010-07-31
Completion date
2013-07-31
Last updated
2014-12-09

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

Conditions

HIV

Keywords

HIV, postpartum, postpartum entry into HIV care

Brief summary

Women with HIV infection in Mississippi who are pregnant or who have had their baby in the past year can agree to fill out a questionnaire about what helps or hurts return to care for HIV infection after having a baby. The combined results should show the most common things that keep women from getting care for HIV infection after having a baby. This will help design another study in order to help more women get into care for HIV infection after having a baby.

Detailed description

Following recruitment and completion of informed consent, a participant will be given a questionnaire to look at factors that help or hinder access to HIV care after delivery. After finishing the initial questionnaire the participant will get a Wal-Mart gift card for $15. The participant may then be asked to complete a longer interview for which she would receive an additional gift card for $25. The combined results will be used to design an interventional study to improve entry into HIV care after delivery.

Interventions

None listed

Sponsors

Brown University
CollaboratorOTHER
University of Mississippi Medical Center
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* age 18 years or older * women with HIV infection who are pregnant or up to 2 months postpartum * English speaking * able to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
linked to long-term HIV carewithin six months of deliveryretrospective chart review for documentation of visit attendance

Secondary

MeasureTime frameDescription
assessment for depressioncross-sectional at time of study visituse of Edinburgh depression screening tool
assessment of intimate partner violencecross-sectional at time of study visituse of WEB (Women's Experience with Battering) screening tool
assessment of stigmacross-sectional at time of study visituse of HIV Related Experiences screening tool
attended a postpartum visitwithin six months of deliveryretrospective chart review for documentation of visit attendance

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026