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Clinical Trials/NCT00408733
NCT00408733
Completed
Not Applicable

Evaluating a Low-Literacy Discharge Medication Education Tool

University of California, Los Angeles1 site in 1 country287 target enrollmentJanuary 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Congestive Heart Failure
Sponsor
University of California, Los Angeles
Enrollment
287
Locations
1
Primary Endpoint
Self-Reported Medication Adherence
Status
Completed
Last Updated
18 years ago

Overview

Brief Summary

Recent studies have demonstrated that patients sub-optimally understand hospital discharge medication instructions Health literacy has been shown to be an important factor in patient understanding of medical information , and following medication instructions.

The primary aim of this project is to test the efficacy of a low-literacy discharge medication education tool on medication adherence, and patient knowledge and understanding of inpatient discharge medications, in a low-income population with low health literacy levels. This evaluation is a prospective trial with patients randomly assigned to either receiving this tool or receiving the current standard of care. Given the complexity of the discharge medication regimen for the conditions of congestive heart failure (CHF) and coronary artery disease (CAD), and the proven effectiveness of these medications in the post discharge period, this trial will focus on the subpopulation of patients hospitalized with these two conditions.

Registry
clinicaltrials.gov
Start Date
January 2007
End Date
August 2007
Last Updated
18 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patient inclusion criteria will be:
  • 18 years of age or greater
  • Admission to the internal medical or cardiology services at LAC/USC Medical Center
  • Discharge directly from the medical service to home
  • During admission, being evaluated or treated for congestive heart failure or coronary artery disease.
  • Patient Exclusion criteria :
  • Moderate or severe cognitive dysfunction
  • Severe psychiatric disability such that the patient has, or there is an application for, a conservator, or any psychiatric illness with current psychotic features
  • Not having speaking proficiency in either English or Spanish language.
  • If the patient was previously enrolled in the study on a prior hospitalization, he or she will also be excluded.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Self-Reported Medication Adherence

Time Frame: 2 & 4 weeks post discharge

Secondary Outcomes

  • Medication Knowledge, Patient Satisfaction & Self-Efficacy, Readmissions and Emergency Department Visits(2weeks -8weeks post discharge)

Study Sites (1)

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