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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01968291
Other study ID # 201206011
Secondary ID
Status Completed
Phase N/A
First received October 10, 2013
Last updated October 22, 2013
Start date June 2012
Est. completion date August 2012

Study information

Verified date October 2013
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 254
Est. completion date August 2012
Est. primary completion date August 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility 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 Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Behavioral:
Teach-back
Patients are asked to repeat back in their own words their understanding of the discharge information that was provided to them.

Locations

Country Name City State
United States Barnes-Jewish Hospital Emergency Department St. Louis Missouri

Sponsors (1)

Lead Sponsor Collaborator
Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other patient satisfaction 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). No
Primary Objective comprehension 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). No
Secondary self-reported comprehension 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). No
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