RECRUITING

Measuring Patient Reported Needs in Outpatient Liver Disease Management

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

This prospective study aims to assess health-related social needs (HRSNs) among patients with chronic liver disease (CLD) receiving outpatient care at Indiana University Health. Patients with CLD often face socioeconomic challenges that adversely affect health outcomes, but no validated screening tool exists for this population. The primary objective is to measure the prevalence and types of HRSNs in CLD patients. Secondary objectives are to evaluate patient preferences regarding provider involvement in addressing social needs, explore reasons for declining assistance, and assess provider perspectives on incorporating HRSN data into clinical care. A total of 200 adult patients with CLD and their visit providers will be enrolled. Participants will complete surveys on demographics, HRSNs, health literacy, quality of life, social support, and patient activation, with medical data supplemented from chart review. Providers will complete surveys about their experiences using HRSN data in routine practice. Results will describe unmet social needs in this population, patient and provider attitudes toward screening, and inform strategies for integrating HRSN assessments into liver disease management and routine healthcare delivery.

Official Title

Measuring Patient Reported Needs in Outpatient Liver Disease Management

Quick Facts

Study Start:2024-03-05
Study Completion:2027-05-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07191886

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. * Patient Inclusion criteria
  2. * Age 18 or greater
  3. * English speaking
  4. * Ability to give consent (West Haven stage 0-1 if history of hepatic encephalopathy)
  1. * Patient Exclusion criteria
  2. * History of liver transplant
  3. * Individuals not willing to participate in the survey
  4. * Patients with severe cognitive impairment

Contacts and Locations

Study Contact

Savannah Yarnelle
CONTACT
3172786424
samussel@iu.edu

Study Locations (Sites)

Indiana University School of Medicine
Indianapolis, Indiana, 46202
United States

Collaborators and Investigators

Sponsor: Indiana 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 Date2024-03-05
Study Completion Date2027-05-30

Study Record Updates

Study Start Date2024-03-05
Study Completion Date2027-05-30

Terms related to this study

Keywords Provided by Researchers

  • health-related social needs
  • social determinants of health
  • patient-reported outcomes
  • quality of life

Additional Relevant MeSH Terms

  • Chronic Liver Disease
  • Cirrhosis, Liver