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NCT00715923 · ClinicalTrials.gov registry record · NA

Modified Consent Form Utility

A NA study, sponsored by University of California, Davis.

Terminated
Registry status
NA
Development phase
30
Enrollment target

NCT00715923 is a NA study that was terminated before completion, run by University of California, Davis. The registered enrollment target is 30 participants.

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The verdict

NCT00715923, a NA study, was terminated before completion, sponsored by University of California, Davis.

TERMINATED
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

Subjects enrolling into a nutrition study of the effects of tea on fat absorption will be randomized to receive either a standard informed consent document or a modified document that is shorter and more easily understood than the standard document. The hypothesis is that using a shorter form that is more easily understood and more visually simple will lead to greater subject satisfaction in the consent process and will not compromise subject comprehension of key study aspects. Consent for study inclusion has been waived by the IRB because informing subjects of the nature and process of the study would likely affect the findings, and both the standard and modified consent forms were approved for use in the nutrition study.

Interventions

  • OTHER Modified consent form
  • OTHER Standard consent form

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2007-11
Est. Completion 2008-12
Phase NA

Sponsor

University of California, Davis

657 total trials

What the Registry Record Tells You About NCT00715923

The ClinicalTrials.gov registry entry for NCT00715923 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, Davis, which has 657 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Modified consent form is the first listed.

NCT00715923 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00715923 about?

NCT00715923 is a clinical study titled "Modified Consent Form Utility". Subjects enrolling into a nutrition study of the effects of tea on fat absorption will be randomized to receive either a standard informed consent document or a modified document that is shorter and more easily understood than the standard document. The hypothesis is that using a shorter form that i...

What is the current status of trial NCT00715923?

This trial is currently terminated. It is a NA study. The enrollment target is 30 participants. The study started on 2007-11. Estimated completion is 2008-12.

What interventions are being tested in trial NCT00715923?

The interventions under investigation include: Modified consent form (OTHER), Standard consent form (OTHER).

Who is sponsoring clinical trial NCT00715923?

This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.