- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01790360
Seek, Test, and Retain. Linkages for Black HIV+, Substance-Using MSM (STAR)
April 4, 2022 updated by: Columbia University
Seek, Test, and Retain. Linkages for Black HIV+, Substance-Using Men Who Have Sex With Men.
The study will seek and recruit substance-using Black Men who have Sex with Men (MSM) in New York City for Human Immunodeficiency Virus (HIV) testing and will link and retain those who are HIV infected in HIV primary care.
The STAR study has two primary objectives: to evaluate the feasibility and effectiveness of Respondent Driven Sampling (RDS) in the substance using Black MSM population for identifying individuals who are HIV infected and not in care; and to assess the relative effectiveness of patient navigation and financial incentives in linkage and retention to HIV care.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The HIV epidemic in the United States most severely affects men who have sex with men (MSM): 61% of all new infections occur in this population.
Black MSM bear a disproportionate burden, with prevalence of 28%, in contrast to 19% in MSM overall.
Black MSM undergo HIV testing less frequently than other MSM; are less likely to be aware that they are HIV infected; are more likely to experience delays in entry into HIV care; and are less likely to be prescribed antiretroviral therapy (ART) when eligible.
These disparities are pronounced in substance-using MSM, as substance users are at elevated risk of late diagnosis and delayed engagement in HIV care.
The combination of pervasive stigma associated with MSM behavior and high rates of substance use hinders effective prevention efforts in this population, even as the prevalence of infection in Black MSM in some US cities approaches 50%.
Reducing HIV-related disparities in MSM and among Black Americans are National HIV/AIDS Strategy priorities and are essential to the effort to control and prevent HIV/AIDS in the US.
Study Type
Interventional
Enrollment (Actual)
1930
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
New York, New York, United States, 10027
- Harlem Prevention Center
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 99 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Self-identify as Black, African American, Caribbean Black, or multi-ethnic Black
- Identify as male
- Greater than 18 years old
- Have had sex with a man during the preceding 12 months
- Have ever used illicit drugs or alcohol to intoxication
Exclusion Criteria:
*Participation in other study assessing linkage and retention in HIV care
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Patient Navigation (PN)
Behavioral Intervention: 'Patient Navigation (PN) Intervention' participants will receive support from navigators in choosing a provider and remembering to attend appointments
|
Patient Navigation is defined as an individual relationship between a navigator and participant to promote retention in the continuum of HIV care .
For this study, three experienced navigators will be hired.
Their primary role will be to ensure that participants are linked to an HIV primary care provider, that they attend at least one scheduled visit within three months of receiving a confirmed HIV diagnosis, and that they are retained in care (as defined by attending three HIV visits within nine months of diagnosis).
To promote linkage to HIV care, navigators will help participants identify material and other barriers to accessing care and will work with participants to overcome those barriers.
Other Names:
|
|
Experimental: Financial Incentives (FI)
Behavioral Intervention: 'Financial Incentives (FI) Intervention' participants will receive gift cards and money for attending clinic visits
|
After confirmation that they have completed their first HIV primary care visit, Financial Incentive participants will receive a gift card.
Additionally, the coordinator will flip a coin and give participants a bonus gift card if the coin flip comes up heads.
Participants who attend the second HIV primary care visit will receive a gift card.
Patients who attend a third HIV primary care visit will receive a gift card.
Study staff will be responsible for confirming participants' attendance at appointments.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Retention Rate (Linkage to Care)
Time Frame: Up to 3 months from HIV diagnosis
|
Linkage to care will be defined as the attendance of at least one scheduled HIV primary care visit within three months of receiving a confirmed HIV diagnosis.
Retention in care will be defined as three visits within nine months of HIV diagnosis.
|
Up to 3 months from HIV diagnosis
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dollars per patient linked and retained in care
Time Frame: Up to 9 months
|
We will calculate dollars per patient linked and retained in care to measure cost-effectiveness of the two linkage/retention interventions: costs administering the incentives for the financial incentives arm and staffing costs for the peer navigation arm.
All such values will then be adjusted by the opportunity cost of each participant's time.
In addition, we will include fixed costs (eg, pamphlets and teaching materials to train the navigators) and the cost of space required to host the navigators.
|
Up to 9 months
|
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Proportion of substance-using Black MSM who are recruited
Time Frame: Up to 3 years
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Effectiveness of Respondent-Driven Sampling (RDS) for seeking and recruiting substance-using Black MSM: the characteristics of RDS will be estimated using conventional proportion calculations, with confidence intervals.
|
Up to 3 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Wafaa M El-Sadr, MD, Columbia University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 1, 2011
Primary Completion (Actual)
September 1, 2016
Study Completion (Actual)
November 17, 2021
Study Registration Dates
First Submitted
January 7, 2013
First Submitted That Met QC Criteria
February 11, 2013
First Posted (Estimate)
February 13, 2013
Study Record Updates
Last Update Posted (Actual)
April 6, 2022
Last Update Submitted That Met QC Criteria
April 4, 2022
Last Verified
April 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- AAAI1585
- 1R01DA032100-01 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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