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The Age of OrthoInfo: A Randomized Controlled Trial Evaluating Patient Comprehension of Informed Consent in a Private Practice

NCT02694237 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2016-05-02

No results posted yet for this study

Summary

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

Conditions

Interventions

BEHAVIORAL

Model

Each participant will receive an informed consent discussion with the aid of an anatomic knee model.

BEHAVIORAL

Knee Anatomy Video

Each participant will hear a scripted informed consent discussion while they watch a knee anatomy video orated by an interviewer.

BEHAVIORAL

Verbal

Each participant will receive a verbal informed consent discussion without a visual aid.

Sponsors & Collaborators

  • University of Missouri, Kansas City

    lead OTHER

Principal Investigators

  • Nkem Egekeze, MD · UMKC Department of Orthopaedic Surgery

  • Karen Williams, PhD · UMKC Department of Health Insight and Research

  • Luv Singh, MD · UMKC Department of Orthopaedic Surgery

  • Dan Gurba, MD · Dickson-Diveley Orthopaedic Clinic

  • Charles Rhoades, MD · UMKC Department of Orthopaedic Surgery

  • Mark Bernhardt, MD · UMKC Dept of Orthopaedic Surgery

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-03-31
Primary Completion
2016-04-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02694237 on ClinicalTrials.gov