Modified Consent Form Utility

Stopped early · Not applicable

Conditions studied: Healthy

In brief

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.

Key facts

Study ID

NCT00715923

Run by

University of California, Davis

People needed

30

Starts

2007-11-01

Expected to finish

2008-12-01

Last updated by the study team

2015-12-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• participation in parent study, English speaking

You may not qualify if…

• none

Where it is running

• University of California Davis — Sacramento, California, United States

Full record on ClinicalTrials.gov

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