Violence and HIV Risk Among Women

Completed · Not applicable

Conditions studied: HIV Risk Reduction

In brief

The purpose of the study is to test the feasibility, acceptability, and efficacy of an adapted intervention that is theoretically and empirically guided by the Information-Motivation-Behavioral skills model (IMB) and aims at reducing sexual risk behavior among women who have experienced Intimate Partner Violence (IPV), as well as such an intervention.

Key facts

Study ID

NCT01695694

Run by

University of Rochester

People needed

120

Starts

2012-09-01

Expected to finish

2013-10-01

Last updated by the study team

2014-02-19

Who can join

Age: 18 and older, up to 49. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women will be eligible to participate in the research study if they meet the following criteria:
• between ages 18 and 49;
• heterosexually active;
• have experienced intimate partner violence in the last three months;
• have engaged in risky sexual behavior in the past three months;
• not currently pregnant or trying to become pregnant; and
• physically and psychologically capable of providing informed consent. All subjects will be required to provide written informed consent prior to enrolling in the study.

You may not qualify if…

• Persons who meet one or more of the following criteria will be excluded from the study:
• men;
• women who have active psychosis or impaired mental status (confirmed with a Mini-Mental Status Exam);
• are unable to understand spoken English;
• are less than 18 years old or greater than 49 years old;
• are currently pregnant or trying to become pregnant
• women who are exclusively in same-sex relationships.

Where it is running

• University of Rochester — Rochester, New York, United States

Full record on ClinicalTrials.gov

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