Can a One-Page handout make drug info easier to understand?
NCT ID NCT06320808
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a new one-page FDA medication handout is more useful and easier to understand than the current drug information insert. 330 women aged 18-45 reviewed one of three handouts and answered questions about readability, usefulness, and comprehension. The goal is to improve how medication information is presented to patients.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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330 people
The number who actually took part.
- Started
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Mar 2024
- Finished
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Feb 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * US geographic location * 18-45 years of age * assigned female sex at birth Exclusion Criteria: * \<18 years of age * \> 45 years of age * assigned a sex other than female at birth
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Carnegie Mellon University
Pittsburgh, Pennsylvania, 15213, United States
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Other studies related to the condition(s) this trial covers.
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