RECRUITING

Predictors of Health Service Utilizations Among Key Population in Washington DC

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 primary objective of the proposed study is to investigate how PrEP use might result in an increase in the utilization of health and social services offered at a local community-based organization. Our primary hypothesis is that the investigators will observe higher utilization of sexual health (STI screenings), psychosocial health (psychotherapy, and substance use treatment) and other social services (emergency cash assistance, food pantry, transportation assistance, clothing,and housing resources) among PrEP users (LAI-PrEP or daily oral) compared to participants who are PrEP naïve over the 12-month follow-up period.

Official Title

A Mixed Methods Study of the Association Between LAI PrEP Initiation and Adherence, and Utilization of Health and Social Support Services Among Key Populations in Washington DC

Quick Facts

Study Start:2023-08-25
Study Completion:2026-01-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06046079

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * age of 18 years or above;
  2. * confirmed HIV-negative status;
  3. * residence in the Washington, DC metropolitan area;
  4. * one of the following PrEP profiles (PrEP naïve \[no history of any PrEP use in the past\] currently on daily oral PrEP or receiving LAI-PrEP).
  1. * being younger than18 years of age
  2. * being unable to speak and/or read English
  3. * a reported residence outside of the defined Washington, DC metropolitan area
  4. * being unable or unwilling to provide written informed consent
  5. * being unable to comply with the requirements of the protocol (i.e. persons with mental health conditions, persons who are intoxicated or incoherent for other reasons)
  6. * evidence of suspected hepatoxicity

Contacts and Locations

Study Contact

DeMarc Hickson, PhD
CONTACT
6786139827
dhickson@uhupil.org

Study Locations (Sites)

Us Helping Us, People into Living Inc
Washington, District of Columbia, 20010
United States

Collaborators and Investigators

Sponsor: Us Helping Us, People Into Living, Inc.

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 Date2023-08-25
Study Completion Date2026-01-01

Study Record Updates

Study Start Date2023-08-25
Study Completion Date2026-01-01

Terms related to this study

Additional Relevant MeSH Terms

  • Pre-exposure Prophylaxis
  • HIV
  • Health Behavior