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NCT01840722 · ClinicalTrials.gov registry record · NA

Brief Intervention for Rural Women at High Risk for HIV/HCV

A NA study, sponsored by Michele Staton.

Completed
Registry status
NA
Development phase
400
Enrollment target

NCT01840722: Completed NA study, sponsored by Michele Staton.

NCT01840722 is a NA study that has completed, run by Michele Staton. The registered enrollment target is 400 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (72% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01840722, a NA study, has completed, sponsored by Michele Staton.

COMPLETED
Registry status
NA
Development phase
400 participants
Enrollment target

Study Summary

The overall aim of this study is to reduce risk behaviors and increase health and behavioral health service utilization among disadvantaged, drug-using rural women at high risk for HIV and HCV. This project has potential to make a significant contribution to science by providing knowledge about the health, risk behaviors, and service utilization of a vulnerable and understudied group of women during a time of emerging and significant public health risk in a rural Appalachian setting. Successful completion of the aims of this project will advance the delivery of a low-cost, potentially high impact intervention with implications for a number of other real world settings (such as criminal justice venues) where other disadvantaged high-risk drug users can be identified and targeted for intervention.

Primary Outcome

Had unprotected sex with a casual partner or when trading sex for money, drugs, etc in the past 6 months

Interventions

  • OTHER MI-based HIV Risk Reduction

Trial Details

FieldValue
Enrollment Target 400 participants
Start Date 2012-12
Est. Completion 2019-05
Phase NA
Michele Staton

5 total trials

What the finished NCT01840722 record still lists

NCT01840722 is an interventional study that assigns participants to a tested intervention. The registered 400 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (72% lower).

The record links to 0 conditions, and to 1 intervention - of which MI-based HIV Risk Reduction is the first listed.

NCT01840722 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01840722 about?

NCT01840722 is a clinical study titled "Brief Intervention for Rural Women at High Risk for HIV/HCV". The overall aim of this study is to reduce risk behaviors and increase health and behavioral health service utilization among disadvantaged, drug-using rural women at high risk for HIV and HCV. This project has potential to make a significant contribution to science by providing knowledge about the ...

What is the current status of trial NCT01840722?

This trial is currently completed. It is a NA study. The enrollment target is 400 participants. The study started on 2012-12. Estimated completion is 2019-05.

What interventions are being tested in trial NCT01840722?

The interventions under investigation include: MI-based HIV Risk Reduction (OTHER).

Who is sponsoring clinical trial NCT01840722?

This trial is sponsored by Michele Staton, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01840722's enrollment target sits among peer trials

400 246th of 2000 higher than 1,734 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01840722, the US trial registry maintained by the National Library of Medicine. NCT01840722 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.