4291.0: Tuesday, November 14, 2000 - 5:15 PM

Abstract #14416

Women-FIT: a pilot study to reduce sexual risk of HIV/STD in drug-using women

Erica L Gollub, DrPH1, David Metzger, PhD1, Ken Mayer, MD2, Beryl Koblin, PhD3, Delinda Mercer, PhD1, Annet Davis-Vogel, MSW1, Anne Coletti, MA4, and George Seage, PhD4. (1) Treatment Research Center, University of Pennsylvania, 3900 Chestnut St - Bldg 3, Phila, PA 19063, 215-823-4533, Gollub_E@research.trc.upenn.edu, (2) Brown University, Providence, RI, (3) New York Blood Center, New York, NY, (4) Abt, Associates, Cambridge, MA

Objective: To test the feasibility of a group intervention for drug-using women at persistent high sexual risk of HIV/STD. Methods: Subjects from a completed HIVNET study (VPSII) who showed continued high levels of sexual risk were recruited in Philadelphia, Providence and New York, to test an intensive group-based behavioral intervention, in a randomized trial. 45-81% of women in the target population reported crack use; 20-22% reported anal sex; 39-77% reported sex trade. The intervention approach has demonstrated behavior change in other populations. Intervention sessions (~2 hrs) aim to: increase knowledge of the anatomy and risk of HIV/STD; increase knowledge and use of a hierarchy of risk-reduction methods, including male and female condoms, diaphragm, cervical cap, spermicide; and improve reproductive health, including enhanced accessing of community health/other services. Protection supplies were provided free. Counseling was conducted by "near-peers" who were provided training and ongoing oversight. The comparison arm received Enhanced HIV testing and counseling, including information on the female and male condoms, and free supplies. Results: Pre-study focus group data on 21 women indicated a high level of interest in this study, including a 82% appearance rate at the group sessions. Feasibility data to be presented on 180 subjects will include: rate of enrollment, participation rate at group sessions; pre-post intervention 'body and methods knowledge' scores at 2 months; and indices of intervention acceptability. Conclusion: Evidence from 180 women in 3 cities will provide data as to whether a full-scale trial of this intervention, with a longer FU interval, is justified.

Learning Objectives: To assess the feasibility of a novel safer-sex intervention directed at drug-using women

Keywords: HIV Interventions, Women and HIV/AIDS

Presenting author's disclosure statement:
Organization/institution whose products or services will be discussed: None
I do not have any significant financial interest/arrangement or affiliation with any organization/institution whose products or services are being discussed in this session.

The 128th Annual Meeting of APHA