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Clinical Trials/NCT05616312
NCT05616312
Recruiting
N/A

Validating a "Teach-back" Protocol to Improve Recall in Orthopedic Trauma Patients

University Hospitals Cleveland Medical Center1 site in 1 country216 target enrollmentOctober 13, 2022

Overview

Phase
N/A
Intervention
Educational Teach Back
Conditions
Education After Trauma
Sponsor
University Hospitals Cleveland Medical Center
Enrollment
216
Locations
1
Primary Endpoint
Number of correct answers to the recall-assessing items on the follow-up questionnaire.
Status
Recruiting
Last Updated
3 months ago

Overview

Brief Summary

The purpose of this study is to evaluate whether receiving education after trauma surgeries affects three things: 1) knowledge about injury and treatment ("recall"), 2) how well patients follow treatment recommendations, and 3) how satisfied patients are with their care. To do so, some participants in this study will receive education, and some will not.

Registry
clinicaltrials.gov
Start Date
October 13, 2022
End Date
December 1, 2026
Last Updated
3 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

John Sontich

Physician

University Hospitals Cleveland Medical Center

Eligibility Criteria

Inclusion Criteria

  • Isolated open or closed fracture of the pelvis and/or lower extremity treated surgically

Exclusion Criteria

  • Patient receiving orthopedic care or follow-up at another institution
  • Non-English speaking
  • Incarcerated (or likely impending incarceration)
  • Currently enrolled in a study that does not permit co-enrollment
  • Traumatic brain injury, dementia, or other cognitive impairment

Arms & Interventions

Postoperative teach-back educational program

Patients will receive teach-back education while they fill out questionnaires.

Intervention: Educational Teach Back

Control

Patients will not receive any teach-back education while filling out questionnaires.

Outcomes

Primary Outcomes

Number of correct answers to the recall-assessing items on the follow-up questionnaire.

Time Frame: Up to 45 minutes

Adherence rate to postoperative weightbearing instructions as measured by patient report.

Time Frame: Up to 180 days post op

Adherence rate to DVT prophylaxis instructions as measured by patient report.

Time Frame: Up to 180 days post op

Mean satisfaction as measured by follow-up questionnaire.

Time Frame: Up to 180 days post op

Satisfaction will be measured on a Likert scale from 1-5 with 1 being very dissatisfied and 5 being very satisfied with care

Study Sites (1)

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