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Rapid HIV Testing and Counseling in High Risk Women in Shelters

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01866046
First Posted: May 31, 2013
Last Update Posted: March 26, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborators:
Brown University
The Miriam Hospital
Indiana University
Information provided by (Responsible Party):
Dawn Johnson, The University of Akron
  Purpose
This is a developmental study evaluating a new rapid HIV testing and risk prevention intervention for residents of battered women's shelters who endorse risky sexual behaviors.

Condition Intervention Phase
HIV Risk Behavioral: RESPECT-IPV Phase 1

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Rapid HIV Testing and Counseling in High Risk Women in Shelters

Resource links provided by NLM:


Further study details as provided by Dawn Johnson, The University of Akron:

Primary Outcome Measures:
  • number of unprotected sexual occasions [ Time Frame: up to 3 months post shelter ]
    Calendar assessment of number of unprotected sexual occasions


Enrollment: 98
Study Start Date: January 2013
Study Completion Date: March 2015
Primary Completion Date: October 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: RESPECT-IPV
Rapid HIV testing and risk prevention intervention for victims of intimate partner violence
Behavioral: RESPECT-IPV
rapid HIV testing intervention and behavioral counseling session where identify risks and develop a risk reduction plan

  Show Detailed Description

  Eligibility

Information from the National Library of Medicine

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, Learn About Clinical Studies.


Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • intimate partner violence and at least one unprotected sexual occasion 3 months prior to entering shelter

Exclusion Criteria:

  • HIV positive
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01866046


Locations
United States, Ohio
University of Akron
Akron, Ohio, United States, 44325
Sponsors and Collaborators
The University of Akron
Brown University
The Miriam Hospital
Indiana University
  More Information

Responsible Party: Dawn Johnson, Associate Professor, The University of Akron
ClinicalTrials.gov Identifier: NCT01866046     History of Changes
Other Study ID Numbers: R21NR013628-02 ( U.S. NIH Grant/Contract )
First Submitted: May 28, 2013
First Posted: May 31, 2013
Last Update Posted: March 26, 2015
Last Verified: March 2015

Keywords provided by Dawn Johnson, The University of Akron:
battered women
HIV risk
STI risk


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