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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 is a NA study that has completed, run by Carnegie Mellon University. The registered enrollment target is 500 participants.
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.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03416907
The ClinicalTrials.gov registry entry for NCT03416907 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 500 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Carnegie Mellon University, which has 37 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 5 interventions - of which Original consent form is the first listed.
NCT03416907 reports 0 study locations.
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.
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