The objective of this study is to assess whether modafinil treatment promotes abstinence and reduces highrisk sexual behavior associated with HIV seroconversion (HRSB) in women who are addicted to cocaine.Preventing the heterosexual transmission of AIDS is arguably the greatest challenge that currently confrontsthe medical community. Women addicted to cocaine are at great risk of HIV seroconversion when theyengage in HRSB (e.g., trading sex for cocaine, having unprotected sex with multiple partners) to obtaincocaine, which is readily available within urban communities. An effective means of identifying and treatingthese women should reduce HRSB that jeopardizes them, their sexual partners, and their partners' partners.This project will utilize a mobile outreach van (MOV) that places our research team in the center of WestPhiladelphia neighborhoods where cocaine is heavily trafficked and consumed, allowing us to identifywomen in urgent need of education and addiction treatment. After informed consent and a comprehensivemedical/psychiatric screening, qualifying subjects will receive HIV testing with pre-test and post-testcounseling designed to provide effective education regarding HIV transmission. Subjects will then berandomized to modafinil (300 mg/day) or placebo treatment for a period of 8 weeks with study medicationsdispensed and monitored in the MOV to optimize subject convenience and medication adherence. Modafinilis a promising agent that blocks cocaine-induced euphoria under controlled conditions, and was recentlyreported to promote cocaine abstinence in a controlled pilot study. Psychosocial treatment will involveTelephone Monitoring and Adaptive Counseling (TMAC), an innovative and cost-effective approach thatprovides a feasible means of treatment delivery to the target population. Cocaine abstinence will bemeasured objectively with twice weekly urine testing and HRSB will be measured with the Risk AssessmentBattery (RAB). Follow-up assessments will be scheduled 3 and 6 months after randomization to furtherassess cocaine abstinence and HRSB. Subjects will be genotyped to assess genetic vulnerability to cocainedependence and pharmacogenetic factors associated with their response to modafinil. Thus, this projectemploys innovative means of identifying, treating, and characterizing a target population in need of effectivetreatment designed to promote recovery and prevent HRSB.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Comprehensive Center (P60)
Project #
2P60DA005186-21
Application #
7343489
Study Section
Special Emphasis Panel (ZDA1-RXL-E (29))
Project Start
2007-07-01
Project End
2012-06-30
Budget Start
2007-07-01
Budget End
2008-06-30
Support Year
21
Fiscal Year
2007
Total Cost
$437,857
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Franklin, Teresa R; Jagannathan, Kanchana; Hager, Nathan et al. (2018) Brain substrates of early (4h) cigarette abstinence: Identification of treatment targets. Drug Alcohol Depend 182:78-85
Wetherill, Reagan R; Jagannathan, Kanchana; Hager, Nathan et al. (2016) Influence of menstrual cycle phase on resting-state functional connectivity in naturally cycling, cigarette-dependent women. Biol Sex Differ 7:24
Woody, George E; Krupitsky, Evgeny; Zvartau, Edwin (2016) Antagonist Models for Relapse Prevention and Reducing HIV Risk. J Neuroimmune Pharmacol 11:401-7
Van Horn, Deborah H A; Drapkin, Michelle; Lynch, Kevin G et al. (2015) Treatment choices and subsequent attendance by substance-dependent patients who disengage from intensive outpatient treatment. Addict Res Theory 23:391-403
Franklin, Teresa R; Jagannathan, Kanchana; Wetherill, Reagan R et al. (2015) Influence of menstrual cycle phase on neural and craving responses to appetitive smoking cues in naturally cycling females. Nicotine Tob Res 17:390-7
Kampman, Kyle M; Lynch, Kevin G; Pettinati, Helen M et al. (2015) A double blind, placebo controlled trial of modafinil for the treatment of cocaine dependence without co-morbid alcohol dependence. Drug Alcohol Depend 155:105-10
Goldman, Marina; Ehrman, Ronald N; Suh, Jesse J et al. (2015) Brief report: ""spiders-No, puppies-Go"", introducing a novel Go NoGo task tested in inner city adolescents at risk for poor impulse control. J Adolesc 38:45-8
McKay, James R; Drapkin, Michelle L; Van Horn, Deborah H A et al. (2015) Effect of patient choice in an adaptive sequential randomization trial of treatment for alcohol and cocaine dependence. J Consult Clin Psychol 83:1021-32
Clarke, T-K; Crist, R C; Ang, A et al. (2014) Genetic variation in OPRD1 and the response to treatment for opioid dependence with buprenorphine in European-American females. Pharmacogenomics J 14:303-8
Clarke, Toni-Kim; Weiss, Amy R D; Ferarro, Thomas N et al. (2014) The dopamine receptor D2 (DRD2) SNP rs1076560 is associated with opioid addiction. Ann Hum Genet 78:33-9

Showing the most recent 10 out of 111 publications