Identifying Undiagnosed Asymptomatic HIV Infection in Hispanic/Latino Adolescents and Young Adults

This study is currently recruiting participants.
Verified October 2012 by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Sponsor:
Collaborators:
Information provided by (Responsible Party):
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
ClinicalTrials.gov Identifier:
NCT01203332
First received: September 15, 2010
Last updated: December 14, 2012
Last verified: October 2012
  Purpose

The proposed research will include adolescent and young adult Hispanic/Latino men who have sex with men (MSM) and heterosexual men and women, aged 13-24 years, and will be based at 13 ATN Adolescent Medicine Trial Units (AMTUs) that provide clinical care and psychosocial services to the target group. In 10 of the 13 sites, comparisons will be made between alternative venue-based testing (AVT) and social and sexual network-based interviewing and HIV testing (SSNIT) strategies to assess which, among these approaches, is the most effective means for identifying undiagnosed human immunodeficiency virus (HIV) in young, at-risk Hispanics/Latinos. Three of the sites will focus solely on use of SSNIT for identifying undiagnosed HIV in our target group of adolescents and young adults. All study participants will complete an audio computer-assisted self-interview (ACASI) and undergo HIV screening. Participants with presumptive HIV positive screening results will be referred to the local AMTU for confirmatory testing, post-test counseling and referrals for linkage to HIV medical care. Linkage to care for ATN 096 study participants will be conducted in accordance with the Strategic Multisite Initiative for the Identification, Linkage, and Engagement in Care of Youth with Undiagnosed HIV Infection (SMILE in CARING for YOUTH) Program (ATN 093), a collaboration of the CDC and NICHD/ATN, to ensure that youth who test positive for HIV as part of this protocol are linked with treatment and care.


Condition Intervention
HIV
Behavioral: Effectiveness of different strategies in HIV testing and linkage to care

Study Type: Observational
Study Design: Observational Model: Ecologic or Community
Time Perspective: Cross-Sectional
Official Title: Identifying Undiagnosed Asymptomatic HIV Infection in Hispanic/Latino Adolescents and Young Adults

Resource links provided by NLM:


Further study details as provided by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD):

Primary Outcome Measures:
  • Effectiveness of AVT strategy with SSNIT [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    To compare the relative effectiveness of AVT with SSNIT, which is a coupon-based index recruiter driven network recruitment strategy for identifying previously undiagnosed HIV infection among Hispanic/Latino adolescents and young adults aged 13-24 years.

  • Facilitators & barriers to HIV testing [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    To examine factors that facilitate and/or hinder Hispanic/Latino adolescents and young adults in getting an HIV test (e.g., perceived risk for HIV, acculturation, homophobia, stigma associated with IDU).

  • Sub-group differences [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    To explore the extent to which sub-group differences (e.g., origin of birth, age, level of acculturation) exist by prevalence of HIV-related risk behaviors, HIV testing, and mode of HIV transmission.


Estimated Enrollment: 5360
Study Start Date: July 2010
Estimated Study Completion Date: January 2013
Estimated Primary Completion Date: January 2013 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Alternative Venue Testing (AVT)
Participants recruited for testing through the AVT recruitment method.
Behavioral: Effectiveness of different strategies in HIV testing and linkage to care
HIV testing Linkage to Care
SSNIT - Index Recruiter
Participants recruited for HIV testing and to bring members of their social and sexual network to the study.
Behavioral: Effectiveness of different strategies in HIV testing and linkage to care
HIV testing Linkage to Care
SSNIT - Network Member
Participants recruited by someone in their social or sexual network to participate in the study, including HIV testing.
Behavioral: Effectiveness of different strategies in HIV testing and linkage to care
HIV testing Linkage to Care

  Eligibility

Ages Eligible for Study:   13 Years to 24 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Adolescent and young adult Hispanic/Latino MSM and heterosexual men and women, aged 13-24 years, who meet all eligibility requirements for enrollment into the AVT or SSNIT component of the study.

Criteria

1. Inclusion Criteria

1a. Alternative Venue-Based Testing (AVT) Participants

  • Self-identifies as being of Hispanic or Latino ethnicity;
  • Provides verbal confirmation that his/her age is between 13 years, 0 days to 24 years, 364 days at the time of enrollment;
  • Self-reports a negative or unknown HIV status;
  • Is male and self-reports any unprotected anal sex with a male sexual partner in the past three months; OR Is female and self-reports any unprotected anal or vaginal sex with two or more male sexual partners in the past three months; OR Is female and self-reports any unprotected anal or vaginal sex with a male sexual partner who was incarcerated in the past 12 months; OR Is male or female and self-reports any history of injection drug use; OR Is male or female and self-reports any unprotected anal or vaginal sex with an individual who is known to be HIV positive; OR Is male or female and self-reports any unprotected anal or vaginal sex with an injection drug user in the past 12 months;
  • Willing to complete an HIV risk assessment;
  • Willing to undergo HIV screening; and
  • Able to understand and willing to provide signed informed consent/assent in English or Spanish.

    1b. Social and Sexual Index Recruiter Participants

  • Self-identifies as being of Hispanic or Latino ethnicity;
  • Provides verbal confirmation that his/her age is between 13 years, 0 days to 24 years, 364 days at the time of enrollment;
  • Is male or female and self-reports being diagnosed with HIV in the past 12 months; OR Is female and self-reports any unprotected anal or vaginal sex with a male sexual partner who was incarcerated in the past 12 months; OR Is male or female and self-reports any history of injection drug use; OR Is male or female and self-reports any unprotected anal or vaginal sex with an individual who is known to be HIV positive; OR Is male or female and self-reports any unprotected anal or vaginal sex with an injection drug user in the past 12 months;
  • Willing to complete a HIV risk assessment;
  • Willing to undergo HIV screening (or an HIV confirmatory test if previously diagnosed);
  • Willing to recruit one or more Latino/Latina family members, friends, or sexual partners who are between the ages of 13-24 years and who meet the criteria for a Social and Sexual Network Member for participation in the study; and
  • Able to understand and willing to provide signed informed consent/assent in English or Spanish.

    1c. Social and Sexual Network Members

  • Self-identifies as being of Hispanic or Latino ethnicity;
  • Provides verbal confirmation that his/her age is between 13 years, 0 days to 24 years, 364 days at the time of enrollment;
  • Self-reports any anal or vaginal sexual activity in the past 3 months and any unprotected anal or vaginal sex in the last 12 months; OR Self-reports any history of injection drug use;
  • Willing to complete a HIV risk assessment;
  • Willing to undergo HIV screening; and
  • Able to understand and willing to provide signed informed consent/assent in English or Spanish.

    1d. Additional Inclusion Criteria for Social and Sexual Network Member Recruiters

  • Is male or female and self-reports being diagnosed with HIV in the past 12 months; OR Is female and self-reports any unprotected anal or vaginal sex with a male sexual partner who was incarcerated in the past 12 months; OR Is male or female and self-reports any history of injection drug use; OR Is male or female and self-reports any unprotected anal or vaginal sex with an individual who is known to be HIV positive; OR Is male or female and self-reports any unprotected anal or vaginal sex with an IDU in the past 12 months; and
  • Willing to recruit one or more Latino/Latina family members, friends, or sexual partners who are between the ages of 13-24 years and who meet the criteria for Social and Sexual Network Members for participation in the study.

    2. Exclusion Criteria

    2a. All Participants

  • Previous participation in ATN 096 as an AVT or a SSNIT study participant;
  • Current or prior participation in ATN 084;
  • Anything that would impair the participant's ability to provide informed consent/assent and/or interfere with the protocol's objectives; i.e., readily apparent psychiatric symptoms (hallucinations, thought disorder), visibly distraught (suicidal, homicidal, exhibiting violent behavior) or visibly intoxicated or under the influence of alcohol or other substances at the time of study enrollment, and
  • Acute illness that, in the opinion of study staff, would interfere with the participant's ability to adhere to the protocol requirements and/or interfere with the protocol objectives.

    2b. Additional Exclusion Criteria for Alternative Venue-Based Testing Participants

  • Self-reports a prior diagnosis of HIV
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01203332

Contacts
Contact: Georgine Price, MPH 301-610-4990 georgineprice@westat.com

Locations
United States, California
Childrens Hospital Los Angeles Recruiting
Los Angeles, California, United States, 90027
Contact: Michelle Bradford, BA     323-361-3161     mbradford@chla.usc.edu    
Principal Investigator: Marvin Belzer, MD            
University of California San Francisco Recruiting
San Francisco, California, United States, 94117
Contact: Tina Clark, FNP     415-290-0895     clarkti@fcm.ucsf.edu    
Principal Investigator: Barbara Moscicki, MD            
United States, District of Columbia
Childrens National Medical Center Terminated
Washington, District of Columbia, United States, 20010
United States, Florida
Childrens Diagnostic & Treatment Center Terminated
Fort Lauderdale, Florida, United States, 33316
University of Miami School of Medicine Recruiting
Miami, Florida, United States, 33101
Contact: Donna Maturo, ARNP     305-243-3442     dmaturo@med.miami.edu    
Principal Investigator: Lawrence Friedman, MD            
University of South Florida Recruiting
Tampa, Florida, United States, 33606
Contact: Tammy Myers            
Principal Investigator: Patricia Emmanuel, MD            
United States, Illinois
Ruth M Rothstein CORE Center/ John H Stroger Jr Hospital Recruiting
Chicago, Illinois, United States, 60612
Contact: Kelly Bojan, DNP, RN, CFNP     (312) 572-4571     kbojan@sbcglobal.net    
Principal Investigator: Jaime Martinez, MD            
United States, Maryland
University of Maryland Recruiting
Baltimore, Maryland, United States, 21201
Contact: Reshma Gorle, MPH     410-706-4153     rgorle@peds.umaryland.edu    
Principal Investigator: Ligia Peralta, MD            
United States, New York
Montefiore Medical Center Recruiting
Bronx, New York, United States, 10467
Contact: Maria Campos, RN     718-882-0023     mcampos@adolescentaids.org    
Principal Investigator: Donna Futterman, MD            
Mount Sinai Medical Center Terminated
NY, New York, United States, 10128
United States, Pennsylvania
Childrens Hospital of Philadelphia Recruiting
Philadelphia, Pennsylvania, United States, 19104
Contact: Adrienne DiBenedetto, BSN     267-426-5527     dibenedettoa@email.chop.edu    
Principal Investigator: Steven Douglas, MD            
United States, Tennessee
St. Jude Childrens Research Hospital Recruiting
Memphis, Tennessee, United States, 38105-2794
Contact: Kristen Branum, BS     901-595-5609     kristen.branum@stjude.org    
Principal Investigator: Patricia Flynn, MD            
Puerto Rico
University of Puerto Rico Recruiting
San Juan, Puerto Rico, 00936-5067
Contact: Hazel Ayala-Flores, BSN     (787) 759-9595     hazel.ayala@upr.edu    
Principal Investigator: Irma Febo, MD            
Sponsors and Collaborators
Investigators
Study Chair: Cherrie B. Boyer, Ph.D. Adolescent Trials Network
Study Chair: Jonathan M. Ellen, M.D. Adolescent Trials Network
  More Information

Additional Information:
No publications provided

Responsible Party: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
ClinicalTrials.gov Identifier: NCT01203332     History of Changes
Other Study ID Numbers: ATN 096
Study First Received: September 15, 2010
Last Updated: December 14, 2012
Health Authority: United States: Federal Government

Keywords provided by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD):
HIV testing
Latino
Latina
Men who have sex with men

Additional relevant MeSH terms:
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
HIV Infections
Acquired Immunodeficiency Syndrome
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Immunologic Deficiency Syndromes
Immune System Diseases
Slow Virus Diseases
HIV Antibodies
Immunologic Factors
Physiological Effects of Drugs
Pharmacologic Actions

ClinicalTrials.gov processed this record on May 16, 2013