Informed Consent Formats by Information Preference and Priority

The goal of this study is to investigate whether the same information can be communicated in
different formats of an informed consent document in ways that improve participant
understanding and confidence. Participants will review one of several different versions of
the same informed consent document, and will be asked to complete a survey after reading the
documents. The survey will ask participants their willingness to enroll in the clinical trial
discussed in the document and their confidence in their decision. The survey will also test
participants recollection of information from the informed consent document. Researchers will
look at this data to see if there are ways to improve knowledge about the clinical trial and
confidence in decisions without necessarily changing enrollment preferences.

Inclusion Criteria:

- 18 Years Old or Older

- Read and agreed to informed consent

- Indicated desire to participate

- Diagnosed with asthma

- US resident

Exclusion Criteria:

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