RECRUITING

Testing Two Interventions to Improve Health Outcomes and Quality of Life Among Rural Older Adults Living With HIV

Conditions

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

Engagement in HIV medical care and adherence to HIV medications are both essential in improving health outcomes among people living with HIV (PLH), but PLH living in rural areas-who suffer higher mortality rates than their urban counterparts-can confront multiple barriers to care engagement and adherence, especially as they face the logistical, medical, and social challenges associated with aging. This project will test the efficacy of two interventions to determine their impact on HIV health outcomes and quality of life among rural, older PLH living in the Southern U.S. The two interventions, adapted from evidence-based interventions and delivered remotely, are: (1) supportive-expressive peer social support groups and (2) strengths-based case management. We hypothesize that both interventions will increase viral suppression, antiretroviral therapy adherence, and health-related quality of life and decrease depressive symptoms. Results from this study will provide us with tools to improve health outcomes for rural older people living with HIV.

Official Title

Testing the Efficacy of Two Interventions to Improve Health Outcomes and Quality of Life Among Rural Older Adults Living With HIV

Quick Facts

Study Start:2024-04-10
Study Completion:2027-01-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06269081

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:50 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Aged 50 years or greater
  2. * Living in a county with a score of .4 or higher on the index of relative rurality (IRR)
  3. * Living in Alabama, Arkansas, Delaware, Florida, Georgia, Kentucky, Louisiana, Maryland, Mississippi, Missouri, North Carolina, Oklahoma, South Carolina, Tennessee, Texas, Virginia, or West Virginia
  4. * Living with HIV
  5. * Has a telephone at home
  6. * Able to provide informed consent
  1. * Not meeting eligibility criteria described above

Contacts and Locations

Study Contact

Jennifer Walsh, PhD
CONTACT
414-955-7710
jwalsh@mcw.edu

Principal Investigator

Jennifer Walsh, PhD
PRINCIPAL_INVESTIGATOR
Center for AIDS Intervention Research, Medical College of Wisconsin
Andrew Petroll, MD
PRINCIPAL_INVESTIGATOR
Center for AIDS Intervention Research, Medical College of Wisconsin

Study Locations (Sites)

Center for AIDS Intervention Research, Medical College of Wisconsin
Milwaukee, Wisconsin, 53202
United States

Collaborators and Investigators

Sponsor: Medical College of Wisconsin

  • Jennifer Walsh, PhD, PRINCIPAL_INVESTIGATOR, Center for AIDS Intervention Research, Medical College of Wisconsin
  • Andrew Petroll, MD, PRINCIPAL_INVESTIGATOR, Center for AIDS Intervention Research, Medical College of Wisconsin

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 Date2024-04-10
Study Completion Date2027-01-31

Study Record Updates

Study Start Date2024-04-10
Study Completion Date2027-01-31

Terms related to this study

Additional Relevant MeSH Terms

  • HIV