RECRUITING

Case Management Dyad

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Conditions

HIVPre-exposure ProphylaxisCase Managementlinkage to careviral suppressionretention in carefinancial wellbeingfood security

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The overall goal of this study is to test whether dyadic and focused case management will (1) improve financial wellbeing, (2) improve access to food, (3) increase linkage and retention rates for individuals living with HIV or those taking PrEP (PrEP persistence), and (4) increase the proportion of individuals living with HIV who are virally suppressed (viral suppression) when compared to routine Ryan White Non-Medical Case Management.

Official Title

Implementation of a Triadic Network Case Management Intervention for Younger Black Sexual Minority Men

Quick Facts

Study Start:2022-09-09
Study Completion:2027-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06162897

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.

Ages Eligible for Study:18 Years to 40 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Black/ African American cis-gender men who have had attraction or sexual activity with a male partner in the past 12 months
  2. * Black/ African American cis-gender women who are living with HIV or vulnerable to HIV (prescribed PrEP or previous sexually transmitted infection (STI) diagnosis)
  3. * Black/African American gender-diverse persons
  4. * Gap in HIV or PrEP care access in the past 24 months, defined as a gap greater than 6 months or detectable viral load at least one time in the past 24 months
  5. * Self-reported financial or food insecurity
  1. * Cis-gender men without attraction or sexual activity with a male partner in the past 12 months
  2. * Cis-gender women who are not living with or vulnerable to HIV (prescribed PrEP or previous STI diagnosis)
  3. * non-Black/African American persons

Contacts and Locations

Study Contact

Rebecca Eavou
CONTACT
773-834-233
reavou@bsd.uchicago.edu

Principal Investigator

John Schneider, MD
PRINCIPAL_INVESTIGATOR
University of Chicago

Study Locations (Sites)

University of Chicago
Chicago, Illinois, 60637
United States

Collaborators and Investigators

Sponsor: University of Chicago

  • John Schneider, MD, PRINCIPAL_INVESTIGATOR, University of Chicago

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 Registration Dates

Study Start Date2022-09-09
Study Completion Date2027-06-30

Study Record Updates

Study Start Date2022-09-09
Study Completion Date2027-06-30

Terms related to this study

Keywords Provided by Researchers

  • linkage to care
  • viral suppression
  • case management
  • retention in care
  • financial wellbeing
  • food security

Additional Relevant MeSH Terms

  • HIV
  • Pre-exposure Prophylaxis
  • Case Management