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Recruiting NCT06435806

Medical Illustration Design Characteristic Evaluation

No phase Interventional Healthy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Medical Illustration design.
Who it may be relevant to
Registry conditions: Healthy. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Advancing Medical Illustration in Patient Education Materials: From Art to Science. Study 1: Medical Illustration Design Characteristic Evaluation

Overview

The goal of this study is to understand what people understand from medical illustrations, and what meaning and emotions (such as anxiety) they derive from different design elements.

Detailed description

The investigators will conduct cognitive interviews to understand the meaning laypersons obtain from different illustrations, their opinions on illustration styles, and their level of anxiety after viewing illustrations.

The investigators will also study the effect of systematically varying medical illustration designs on layperson understanding and anxiety.

Interventions

  • Other Medical Illustration design
    We will test 10 binary design variants for medical illustrations (for example, with and without cut-away, with and without text labels, etc). Specific variants to be identified during first task of project.

Primary outcome measures

  • Knowledge [Time frame: Baseline and 30 minutes]
  • State Anxiety scale from State-Trait Anxiety Inventory [Time frame: 30 minutes]
Secondary outcome measures (3)
  • Satisfaction with the medical illustration [Time frame: 30 minutes]
  • Reading Effort [Time frame: 30 minutes]
  • Acceptability [Time frame: 30 minutes]

Eligibility criteria

Inclusion criteria

  • Over 18 years old
  • Speaks English or Spanish fluently
  • Is able to independently consent
  • Has adequate corrected vision to read patient education documents

Exclusion criteria

\* None

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Single group
Masking
Single blind
Primary purpose
Other

Study locations

United States · 2 centers
  • Tufts Medical Center — Boston
  • Northeastern University — Boston

Identifiers

NCT: NCT06435806 · 427440

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗