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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
  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:


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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

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 November 25, 2014