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Study details
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Implement and Test Visual Consent Template and Process

Washington University School of Medicine
NCT IDNCT06804837ClinicalTrials.gov data as of Apr 2026
Target enrollment

515

Study length

about 1.3 years

Ages

18+

Locations

3 sites in MO, NC, UT

What this study is about

This trial is testing a new way to get consent from people. It involves using a visual template instead of the usual written form. The goal is to see if this method makes it easier for patients to understand what they are agreeing to.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Standard consent
  • 2.Visual consent

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized (Open Label)

You are randomly assigned, but you will know your treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Body systems

Neurology, Oncology