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Multicomponent Intervention to Reduce Sexual Risk and Substance Use

Hunter College of City University of New York logo

Hunter College of City University of New York

Status

Completed

Conditions

Sexually Transmitted Infections
Substance Use
HIV

Treatments

Behavioral: MI + CBST Intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT01880489
R01DA034661 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The objective is to expand and refine an intervention for transgender women (TW) into a 7-session individual- and group-based intervention that is scalable for community settings to reduce sexual risk and substance use and to increase stigma-coping and risk-buffering behaviors among TW in NYC. The investigators will pilot test the intervention with 20 TW and subsequently, conduct a randomized controlled trial with 240 TW to compare the intervention to a wait list control condition.

Enrollment

143 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18 years of age or older
  • Identify as a transgender woman (assigned male at birth and currently identify as female)
  • Report 3 or more acts of unprotected anal or vaginal sex in the past 90 days and at least 1 in the past 30 days
  • Report 5 or more days of illicit drug use in the past 90 days and at least 2 in the past 30
  • Provide contact information
  • Reside in the NYC metropolitan area
  • Able to complete a survey in English (Spanish-language assistance can be provided by bilingual staff)
  • Provide informed consent

Exclusion criteria

  • Unstable, serious psychiatric symptoms
  • Current suicidal/homicidal ideation
  • Evidence of gross cognitive impairment
  • Currently enrolled in a drug abuse treatment or enrolled in an HIV risk or drug use intervention study

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

143 participants in 2 patient groups

MI + CBST Intervention
Experimental group
Description:
Seven sessions of Motivational Interviewing and Cognitive Behavioral Skills Training
Treatment:
Behavioral: MI + CBST Intervention
Wait List Control Condition
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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