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NCT03416907 · ClinicalTrials.gov registry record · NA
Informed Consent Formats by Information Preference and Priority
A NA study, sponsored by Carnegie Mellon University.
- Completed
- Registry status
- NA
- Development phase
- 500
- Enrollment target
NCT03416907: Completed NA study, sponsored by Carnegie Mellon University.
NCT03416907 is a NA study that has completed, run by Carnegie Mellon University. The registered enrollment target is 500 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (64% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03416907, a NA study, has completed, sponsored by Carnegie Mellon University.
- COMPLETED
- Registry status
- NA
- Development phase
- 500 participants
- Enrollment target
Study Summary
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.
Primary Outcome
Sum of correct answers (T/F) for any item relating to material that was rated as 50 or higher on impact on willingness to enroll in a previous study.
Interventions
- BEHAVIORAL Original consent form
- BEHAVIORAL Shortened consent form
- BEHAVIORAL Reordered, shortened consent form
- BEHAVIORAL Shortened consent form with a highlights box
- BEHAVIORAL Interactive, shortened consent form
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 500 participants |
| Start Date | 2017-11-27 |
| Est. Completion | 2017-12-31 |
| Phase | NA |
What the finished NCT03416907 record still lists
NCT03416907 is an interventional study that assigns participants to a tested intervention. The registered 500 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (64% lower).
The record links to 0 conditions, and to 5 interventions - of which Original consent form is the first listed.
NCT03416907 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03416907 about?
NCT03416907 is a clinical study titled "Informed Consent Formats by Information Preference and Priority". 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.
What is the current status of trial NCT03416907?
This trial is currently completed. It is a NA study. The enrollment target is 500 participants. The study started on 2017-11-27. Estimated completion is 2017-12-31.
What interventions are being tested in trial NCT03416907?
The interventions under investigation include: Original consent form (BEHAVIORAL), Shortened consent form (BEHAVIORAL), Reordered, shortened consent form (BEHAVIORAL), Shortened consent form with a highlights box (BEHAVIORAL), Interactive, shortened consent form (BEHAVIORAL).
Who is sponsoring clinical trial NCT03416907?
This trial is sponsored by Carnegie Mellon University, which has 37 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03416907's enrollment target sits among peer trials
500 193rd of 2000 higher than 1,788 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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