RECRUITING

The SINCERE Intervention to Address COVID-19 Health Disparities

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 real world efficacy study is to understand the benefit of universal social needs screening, community-based service referrals, and telephonic follow-up as a scalable strategy for preventing COVID-19 transmission, and for addressing the secondary health effects of the social, behavioral, and economic changes following the COVID-19 pandemic. With statewide community service providers, existing health information technology, and piloted methods, we seek to determine the effectiveness of universal social needs screening and community service referrals - the SINCERE intervention - in improving health outcomes of COVID-19 vulnerable and socioeconomically disadvantaged populations and whether intensive follow-up and collaborative goal-setting helps overcome barriers to community service use by patients seen in the emergency department and seeking COVID testing at community-based and mobile clinic locations.

Official Title

Intensifying Community Referrals for Health: the SINCERE Intervention to Address COVID-19 Health Disparities

Quick Facts

Study Start:2021-09-27
Study Completion:2025-09-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05228886

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. * Adult (\> 17 years)
  2. * English or Spanish speaking
  3. * Completed the referral process at the UHealth ED, one of the COVID-19 testing sites or the Primary Children's ED and indicated both social needs and willingness to receive service low- and no-cost referrals from the United Way 211 community referral service
  4. * Able to be reached by phone during the intervention OR able to complete surveys sent by text or email
  1. * Those unable to communicate verbally
  2. * Those living in nursing facilities, or those who are not otherwise responsible for self-care

Contacts and Locations

Study Contact

Ernest Grigorian
CONTACT
801-707-2775
ernest.grigorian@utah.edu

Principal Investigator

Andrea Wallace, PhD
PRINCIPAL_INVESTIGATOR
University of Utah

Study Locations (Sites)

University of Utah
Salt Lake City, Utah, 84112
United States

Collaborators and Investigators

Sponsor: Andrea Wallace

  • Andrea Wallace, PhD, PRINCIPAL_INVESTIGATOR, University of Utah

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 Date2021-09-27
Study Completion Date2025-09-30

Study Record Updates

Study Start Date2021-09-27
Study Completion Date2025-09-30

Terms related to this study

Additional Relevant MeSH Terms

  • COVID-19
  • Vulnerable Populations
  • Social Determinants of Health