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Search / Trial NCT06356558

Adapting Enhanced Recovery Programs for Low Health Literacy Patients

Launched by UNIVERSITY OF ALABAMA AT BIRMINGHAM · Apr 4, 2024

Trial Information

Current as of July 21, 2025

Not yet recruiting

Keywords

Surgery Health Literacy Enhanced Recovery

ClinConnect Summary

This clinical trial is focused on improving the care of patients with low health literacy who are undergoing surgery. Low health literacy means that some patients may have difficulty understanding medical information, which can lead to longer hospital stays and more complications after surgery. The study will test a program called VISACT, which uses visual aids, helps doctors communicate better, and trains healthcare organizations to support patients with low health literacy. By making these improvements, the researchers hope to enhance recovery programs and ultimately improve patient outcomes.

To participate in this study, individuals must be at least 18 years old and undergoing surgery as part of an enhanced recovery program. Caregivers and healthcare providers involved in the program are also eligible. Participants need to be able to understand and consent to the study, and they must speak English. The trial is not yet recruiting participants, but those who join can expect to be part of a pilot program that aims to create better support systems for patients with low health literacy, helping to reduce disparities in surgical care.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Adult patients \>= 18 years of age undergoing surgery under an enhanced recovery program (ERPs)
  • Adult caregivers/providers, organizational leaders, \>= 18 years of age with direct or indirect involvement with ERP implementation
  • All genders
  • All race/ethnicities
  • Able to consent
  • English-speaking
  • Exclusion Criteria:
  • Child (\<18 years of age)
  • Patients undergoing operations not included under ERPs
  • Participants unable to consent for the study
  • Participants whose mental state excludes them from being able to understand contents of the informed consent form and/or patients whose family members or patient representative do not wish for them to participate in the study

About University Of Alabama At Birmingham

The University of Alabama at Birmingham (UAB) is a prominent academic institution and research hub dedicated to advancing healthcare through innovative clinical trials. Renowned for its commitment to medical discovery and education, UAB conducts cutting-edge research across a wide array of disciplines, including oncology, cardiology, neurology, and public health. With a robust infrastructure for clinical research, UAB fosters collaboration among interdisciplinary teams, leveraging state-of-the-art facilities and resources to enhance the translation of scientific findings into effective treatments and interventions. As a leader in clinical research, UAB aims to improve patient outcomes and contribute to the broader medical community through rigorous trial design and implementation.

Locations

Patients applied

0 patients applied

Trial Officials

Daniel I Chu, MD

Principal Investigator

University of Alabama at Birmingham

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported