- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01968291
Use of Teach Back to Improve Comprehension of Discharge Instructions for Emergency Patients With Limited Health Literacy
October 22, 2013 updated by: Richard Griffey, Washington University School of Medicine
The Impact of Teach-back on Comprehension of Discharge Instructions Among Emergency Patients With Limited Health Literacy: A Randomized, Controlled Study
The purpose of this study was to determine whether use of teach-back discharge instructions improve patient satisfaction and patients' self-reported and objective comprehension of discharge instructions in the emergency department when compared to standard discharge instructions.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
254
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Missouri
-
St. Louis, Missouri, United States, 63110
- Barnes-Jewish Hospital Emergency Department
-
-
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.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- patients being discharged from the emergency department
- A score of 6 or less on the Rapid Estimate of Adult Literacy in Medicine, Revised (consistent with Limited Health Literacy)
Exclusion Criteria:
- aphasia,
- non-English speaking,
- mental handicap,
- psychiatric chief complaint,
- too high acuity per physician,
- insurmountable communication barrier,
- evaluations for sexual assault,
- clinical intoxication.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Teach-back
Patients are prompted to state back in their own words their comprehension of the information given to them at discharge.
|
Patients are asked to repeat back in their own words their understanding of the discharge information that was provided to them.
|
No Intervention: Standard Discharge Instructions
Patient receives usual discharge instructions as administered by the nurse assigned to the patient.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Objective comprehension
Time Frame: Questions evaluating comprehension were administered during the discharge interview immediately following discharge from the ED at the index visit (Day 1).
|
Concordance between audio taped comprehension compared to review of medical record using 5 level scale of concordance
|
Questions evaluating comprehension were administered during the discharge interview immediately following discharge from the ED at the index visit (Day 1).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
self-reported comprehension
Time Frame: Questions evaluating self-reported comprehension were administered during the discharge interview immediately following discharge from the ED at the index visit (Day 1).
|
self reported comprehension of discharge instructions for the following areas: emergency department (ED) course (Tests and treatment); Post-ED care (medication instructions; home instructions; follow-up instructions); Return instructions.
|
Questions evaluating self-reported comprehension were administered during the discharge interview immediately following discharge from the ED at the index visit (Day 1).
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
patient satisfaction
Time Frame: Questions evaluating satisfaction were administered during the discharge interview immediately following discharge from the ED at the index visit (Day 1).
|
Patient satisfaction as measured by 4 questions modified from the Consumer Assessment of Health Providers & Systems (CAHPS) Clinician & Group Surveys
|
Questions evaluating satisfaction were administered during the discharge interview immediately following discharge from the ED at the index visit (Day 1).
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Richard T Griffey, MD, MPH, Washington University School of Medicine
- Principal Investigator: Kim A Kaphingst, PhD, Washington University School of Medicine
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 Major Dates
Study Start
June 1, 2012
Primary Completion (Actual)
August 1, 2012
Study Completion (Actual)
August 1, 2012
Study Registration Dates
First Submitted
October 10, 2013
First Submitted That Met QC Criteria
October 22, 2013
First Posted (Estimate)
October 24, 2013
Study Record Updates
Last Update Posted (Estimate)
October 24, 2013
Last Update Submitted That Met QC Criteria
October 22, 2013
Last Verified
October 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201206011
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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