Text Size

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

This study is enrolling participants by invitation only.
Sponsor:
Collaborator:
Brown University
Information provided by (Responsible Party):
Binford Nash, University of Mississippi Medical Center
ClinicalTrials.gov Identifier:
NCT01190605
First received: August 26, 2010
Last updated: April 5, 2012
Last verified: April 2012
History of Changes
  Purpose

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.


Condition
HIV

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Cross-Sectional
Official Title: Evaluating Factors That Impact Loss to Follow-up Among Postpartum HIV-infected Women in Mississippi

Resource links provided by NLM:

U.S. FDA Resources

Further study details as provided by University of Mississippi Medical Center:

Estimated Enrollment: 75
Study Start Date: July 2010
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.

  Eligibility

Ages Eligible for Study:   18 Years to 45 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Women in Mississippi with HIV infection who have been pregnant and received perinatal HIV care at University of Mississippi Medical Center are eligible to participate in a questionnaire study on the factors that affect entry into HIV care after delivery

Criteria

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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01190605

Locations
United States, Mississippi
University of Mississippi Medical Center
Jackson, Mississippi, United States, 39216-4505
Sponsors and Collaborators
University of Mississippi Medical Center
Brown University
Investigators
Principal Investigator: Binford T Nash, MD University of Mississippi Medical Center
  More Information

No publications provided

Responsible Party: Binford Nash, Asst. Professor, Pediatrics, School of Medicine, University of Mississippi Medical Center
ClinicalTrials.gov Identifier: NCT01190605     History of Changes
Other Study ID Numbers: 2010-0131
Study First Received: August 26, 2010
Last Updated: April 5, 2012
Health Authority: United States: Institutional Review Board

Keywords provided by University of Mississippi Medical Center:
HIV
postpartum
postpartum entry into HIV care

ClinicalTrials.gov processed this record on May 23, 2013