RECRUITING

Enhancing Wellness Through Affirming Services and Education

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 goal of this treatment study is to learn about the mental health, substance use and physical health outcomes associated with participating in the EASE holistic behavioral health and wellness program for individuals identifying as LGBTQ+ and/or living with HIV. The main questions it aims to answer are: 1. Do important health outcomes, including substance use, mental health and social support related outcomes of individuals living with HIV and/or identifying as LGBTQ who participated in the holistic behavioral health and wellness program change after study participation? 2. Does a tailored approach to meet the specific needs of different subpopulations including 1) older (40+) PLWH and/or LGBTQ individuals with or at risk for additional health comorbidities and 2) PLWH and/or LGBTQ young adults (18-40) improve health outcomes including improvement in health and health behaviors . Participants will be asked to: * participate in 6 months of behavioral health treatment tailored to their needs, which may include individual counseling, group counseling, case management, peer support, and related education. * Complete surveys at the time of study entry and 6 months later to measure changes in health outcomes over time.

Official Title

Enhancing Wellness Through Affirming Services and Education

Quick Facts

Study Start:2023-02-13
Study Completion:2027-07-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05700474

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:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. HIV diagnosis or self-identified LGBTQ+
  2. 2. Any alcohol or illicit substance use in the last 90 days
  3. 3. 18 or older
  4. 4. Residing in Mecklenburg County or surrounding areas.
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Susan Reif
CONTACT
17042587111
susan.reif@duke.edu

Principal Investigator

Susan Reif, PhD, MSW
PRINCIPAL_INVESTIGATOR
Duke University

Study Locations (Sites)

Susan Reif
Charlotte, North Carolina, 28207
United States

Collaborators and Investigators

Sponsor: Duke University

  • Susan Reif, PhD, MSW, PRINCIPAL_INVESTIGATOR, Duke University

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 Date2023-02-13
Study Completion Date2027-07-01

Study Record Updates

Study Start Date2023-02-13
Study Completion Date2027-07-01

Terms related to this study

Keywords Provided by Researchers

  • HIV
  • Mental Health
  • Substance Use
  • PrEP
  • Comorbidity

Additional Relevant MeSH Terms

  • HIV
  • Mental Health Disorder
  • Substance Use