HIP: HIV Intervention for Providers
The purpose is to encourage Provider participants to evaluate high risk HIV transmission behaviors and offer prevention messages to their HIV+ patients which will, in turn, reduce rates of unprotected anal and/or vaginal sex with partners of known HIV sero-negativity or unknown HIV serostatus. It is hypothesized that patients of providers participating in the HIP intervention will report higher reduction in sexual risk practices, when compared to the patients of the providers who were randomized into the control condition.
|Study Design:||Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Factorial Assignment
Masking: Open Label
Primary Purpose: Prevention
|Official Title:||HIP: HIV Intervention for Providers|
- Self-reported, unprotected (without condoms) anal or vaginal sex with HIV-negative and unknown-status persons.
|Study Start Date:||June 2004|
|Study Completion Date:||September 2008|
|Primary Completion Date:||October 2006 (Final data collection date for primary outcome measure)|
|United States, California|
|University of California San Francisco - CAPS|
|San Francisco, California, United States, 94105|
|Principal Investigator:||Dogan Eroglu, PhD.||Centers for Disease Control and Prevention|