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Multilevel Influences on HIV and Substance Use in a YMSM Cohort (RADAR)
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Sample details

The RADAR study is designed to provide insights into risk and protective factors for HIV and drug use among young men who have sex with men and transgender women (YMSM). Participants include over 1,000 male individuals, recruited from two previous research projects, Project Q2 and Crew 450, alongside a third cohort of newly recruited individuals and their romantic partners. Those from the previous research projects and newly recruited participants were aged 16 to 20 years old, while their romantic partners could be up to 29 years old. Since the beginning of the study in 2015, participants have been followed up over 15 times, with follow-ups occurring every 6 months.

Study design
Cohort - accelerated

Number of participants at first data collection

1,015 (participants)

Recruitment is ongoing

Age at first data collection

16 - 29 years (participants)

Participant year of birth

Varied (participants)

Participant sex
Male

Representative sample at baseline?
The YMSM population of the city of Chicago in the United States of America.

Sample features

Adolescents
LGBTQIA+ populations
Males
Men who have sex with men (MSM)
Partner dyad
Dataset details

Country

United States of America

Year of first data collection

2015

Primary Institutions

Center on Halsted

Chicago Department of Public Helth (CDPH)

Institute for Sexual and Gender Minority Health (ISGMH)

Northwestern University (NU)

University of Edinburgh (University o Edinburgh, Oilthigh Dhùn Èideann)

Links

isgmh.northwestern.edu/our-research/projects-and-studies/radar/

icpsr.umich.edu/web/ICPSR/studies/37603/summary

Funders

National Institute on Drug Abuse (NIDA)

National Institutes of Health (NIH)

U.S. Department of Health and Human Services (DHHS)

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Interview – face-to-face
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Existing research data
Features

Engagement

  • Community engagement
  • Participant or community advisory groups
  • Patients, service users, lived experience involvement
  • Keywords

    Adolescence
    Biological samples/biospecimens
    Disease detection
    Disease progression
    Health and wellbeing
    Human immunodeficiency virus (HIV)
    Lifestyle factors
    Minority groups
    Racial minorities
    Sexuality and gender identity
    Sexually transmitted infections (STIs)
    Stigma
    Substance use

    Consortia and dataset groups

    The Collaborating Consortium of Cohorts Producing NIDA Opportunities (C3PNO)
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