Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
290 participants
INTERVENTIONAL
2017-10-09
2020-06-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Routine PrEP Care
Routine PrEP Care at each clinical site.
No interventions assigned to this group
WERK Supportive Contact
Support contact will provide emotional support and practical support in order to help their friend/family member to stay engaged in PrEP Care.
WERK Supportive Contact
Provide emotional support and practical support. Support friend/family by helping him to stay engaged in PrEP Care.
Interventions
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WERK Supportive Contact
Provide emotional support and practical support. Support friend/family by helping him to stay engaged in PrEP Care.
Eligibility Criteria
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Inclusion Criteria
* Self-identify as African American/Black;
* Assigned male sex at birth;
* Any same gender anal or oral sex in the past 2 years;
* English speaking;
* Have at least one support contact in their network;
* Own a cell phone not shared with other persons;
* Between the ages of 18-35 years old; and
* Have had fewer than 3 PrEP clinical visits in the past 12 months.
Support Contact:
* Index participant has agreed to including the support contact
* Willing to attend face to face and telephone mini-booster sessions;
* 18 years of age or older;
* English speaking; and
* Owns a cell phone that is not shared with other persons.
Exclusion Criteria
* Unable to provide informed consent;
* Plan to move out of the area within the next 12 months;
* Are not willing to attend intervention sessions; or
* Not willing to return for assessments.
For index participants without a support contact, we will refer them to an appropriate support group for PrEP.
Support Contact:
* Romantic partner of index participant;
* Unable to provide informed consent;
* Plan to move out of the area within the next 12 months;
* Are not willing to attend intervention sessions; or
* Not willing to return for assessments.
18 Years
35 Years
MALE
Yes
Sponsors
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Howard Brown Health Center
OTHER
Ann & Robert H Lurie Children's Hospital of Chicago
OTHER
National Institute of Mental Health (NIMH)
NIH
University of Chicago
OTHER
Responsible Party
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Principal Investigators
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Alida Bouris, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Chicago
Locations
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Chicago Center for HIV Elimination
Chicago, Illinois, United States
Countries
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Other Identifiers
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IRB17-0152
Identifier Type: -
Identifier Source: org_study_id
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