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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02694237
Other study ID # OrthoInfo
Secondary ID
Status Completed
Phase N/A
First received February 18, 2016
Last updated April 28, 2016
Start date March 2016

Study information

Verified date April 2016
Source University of Missouri, Kansas City
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The aim of the study is determine which method of informed consent improves comprehension in college educated patients in a private practice setting.


Recruitment information / eligibility

Status Completed
Enrollment 66
Est. completion date
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Knee osteoarthritis patients over the age of 18 with a college education deemed appropriate for medical management with a knee injection.

Exclusion Criteria:

- Patients without the capacity to provide consent

- Patients with a visual, auditory, psychological or tactile impairment requiring the assistance of another person.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Model
Each participant will receive an informed consent discussion with the aid of an anatomic knee model.
Knee Anatomy Video
Each participant will hear a scripted informed consent discussion while they watch a knee anatomy video orated by an interviewer.
Verbal
Each participant will receive a verbal informed consent discussion without a visual aid.

Locations

Country Name City State
United States Truman Medical Center and Dickson-Diveley Orthopaedic Clinic Kansas City Missouri

Sponsors (1)

Lead Sponsor Collaborator
University of Missouri, Kansas City

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The Nkem Test This knowledge based questionnaire assesses patient comprehension of an informed consent discussion. The score of the test is known as "The Nkem Score". baseline No
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