Informed Consent Formats by Information Preference and Priority

Completed · Not applicable

Conditions studied: Consent Forms, Asthma

In brief

This study will test whether different formats of medical informed consent documents can help improve understanding and confidence in decision-making for clinical trials. The study will be primarily run through an online survey.

Key facts

Study ID

NCT03416907

Run by

Carnegie Mellon University

People needed

500

Starts

2017-11-27

Expected to finish

2017-12-31

Last updated by the study team

2018-01-31

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 18 Years Old or Older
• Read and agreed to informed consent
• Indicated desire to participate
• Diagnosed with asthma
• US resident

You may not qualify if…

• Participants from whom we receive multiple responses will be dropped from analysis (but will be compensated for participation)

Where it is running

• Carnegie Mellon University — Pittsburgh, Pennsylvania, United States

Full record on ClinicalTrials.gov

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