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

NCT01190605 | Completed

• 1 other identifier: 2010-0131
• Study Type: observational
• Target: 53
• Locations: 1 country
• Sites: 1

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.

Conditions

HIV

Keywords

HIV; postpartum; postpartum entry into HIV care

Outcome Measures

Primary Outcomes (1)

• linked to long-term HIV care

  retrospective chart review for documentation of visit attendance

  within six months of delivery

Secondary Outcomes (4)

• assessment for depression

  cross-sectional at time of study visit

• assessment of intimate partner violence

  cross-sectional at time of study visit

• assessment of stigma

  cross-sectional at time of study visit

• attended a postpartum visit

  within six months of delivery

Eligibility Criteria

• Age: 18 Years - 45 Years
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64)
• 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

You may qualify if:

• 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

Sponsors & Collaborators

• University of Mississippi Medical Center: lead
• Brown University: collaborator

Study Sites (1)

University of Mississippi Medical Center

Jackson, Mississippi, 39216-4505, United States

Location

Study Officials

• Binford T Nash, MD

  University of Mississippi Medical Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: CASE ONLY
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Asst. Professor, Pediatrics, School of Medicine

Study Record Dates

• First Submitted: August 26, 2010
• First Posted: August 27, 2010
• Study Start: July 1, 2010
• Primary Completion: September 1, 2012
• Study Completion: July 1, 2013
• Last Updated: December 9, 2014

Record last verified: 2014-12

Locations

US (1)