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Recruiting NCT07191886

Measuring Patient Reported Needs in Outpatient Liver Disease Management

Observational Chronic Liver Disease Cirrhosis, Liver

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Chronic Liver Disease, Cirrhosis, Liver. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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.

Detailed description

Patients with chronic liver disease (CLD) are a medically and socially vulnerable population who often face significant health-related social needs (HRSNs), such as financial strain, housing instability, limited access to transportation, and lack of social support. These unmet needs contribute to poorer health outcomes and higher healthcare utilization, yet there is currently no validated screening tool specifically designed for patients with CLD. In addition, little is known about whether patients want their healthcare providers to address these needs, or how providers might use such information in routine practice.

This study is designed to measure the prevalence of HRSNs in patients with CLD receiving care in outpatient liver clinics, and to explore patient and provider perspectives on the role of HRSN screening in clinical care. Patients will complete surveys assessing HRSNs, health literacy, quality of life, social support, and patient activation, with additional demographic and clinical information obtained from chart review. Providers will complete surveys regarding their experience and potential use of HRSN data.

By combining patient- and provider-reported data, this study will generate new insights into the burden of unmet social needs in CLD, patient preferences for assistance from their care team, and provider attitudes toward incorporating HRSN data into clinical management. Findings are expected to inform the development and implementation of standardized HRSN screening approaches in liver disease care, with the broader goal of improving patient-centered outcomes and aligning with evolving healthcare quality standards.

Primary outcome measures

  • Prevalence and Types of Health-Related Social Needs (HRSNs) [Time frame: Day 1]
Secondary outcome measures (4)
  • Patient Preferences for Provider Involvement in Addressing HRSNs [Time frame: Day 1]
  • Reasons Patients Decline Provider Assistance with HRSNs [Time frame: Day 1]
  • Provider Perspectives on HRSN Screening [Time frame: Within 7 days of patient visit]
  • Association Between HRSNs and Clinical Characteristics [Time frame: Day 1, with retrospective chart review (12 months prior healthcare utilization and labs)]

Eligibility criteria

Inclusion criteria

  • Patient Inclusion criteria
  • Age 18 or greater
  • English speaking
  • Ability to give consent (West Haven stage 0-1 if history of hepatic encephalopathy)

Provider Inclusion Criteria • Participated in patient care during inclusion visit

Exclusion criteria

  • Patient Exclusion criteria
  • History of liver transplant
  • Individuals not willing to participate in the survey
  • Patients with severe cognitive impairment

Provider Exclusion Criteria

  • Unable to complete survey within 7 days of the inclusion visit

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • Indiana University School of Medicine — Indianapolis

Identifiers

NCT: NCT07191886 · PRN Study

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗