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COMPLETED

Evaluation of Barriers to Postpartum Care in HIV Infected Women

NCT01853917 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate why the majority of HIV infected women in the Harris County Health District system who are pregnant do not come to clinic for their HIV disease after they have a baby through questionaires administered prepartum and questionaires and structured interviews postpartum. The study will ask subjects questions about HIV, drug use, depression and social problems.

Conditions Studied

Interventions

  • OTHER questionaires and structured interviews

Study Locations (2)

Texas

  • Harris County Hospital District Clinics-Thomas Street Clinic, Northwest Clinic — Houston
  • Harris County Hospital District Clinics-LBJ hospital — Houston

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2012-01
Est. Completion 2014-11

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01853917

The ClinicalTrials.gov registry entry for NCT01853917 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 38 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 811 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Pregnancy appearing as the primary indexed condition, and to 1 intervention — of which questionaires and structured interviews is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01853917 reports 2 study locations spanning 1 distinct geographic area — top geographies include Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01853917 about?

NCT01853917 is a clinical study titled "Evaluation of Barriers to Postpartum Care in HIV Infected Women". The purpose of this study is to evaluate why the majority of HIV infected women in the Harris County Health District system who are pregnant do not come to clinic for their HIV disease after they have a baby through questionaires administered prepartum and questionaires and structured interviews pos...

What is the current status of trial NCT01853917?

This trial is currently completed. The enrollment target is 38 participants. The study started on 2012-01. Estimated completion is 2014-11.

What conditions does trial NCT01853917 study?

This clinical trial studies the following conditions: Pregnancy, HIV Infection. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01853917?

The interventions under investigation include: questionaires and structured interviews (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01853917?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 811 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01853917 being conducted?

This trial has 2 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial