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The Effects of Coffee

This study has been completed.
Information provided by:
American University Identifier:
First received: June 9, 2006
Last updated: March 14, 2007
Last verified: March 2007
In this study, participants will be eligible to participate in a paid research study that will examine the effects of regular coffee drinking. The study takes approximately 2 hours total, 55 min. on 2 separate days. Participants will be asked to do computer tasks and drink only coffee provided to them during the study.

Condition Phase
Healthy Subjects Phase 1

Study Type: Observational
Study Design: Observational Model: Defined Population
Time Perspective: Cross-Sectional
Time Perspective: Prospective
Official Title: The Effects of Coffee

Further study details as provided by American University:

Estimated Enrollment: 50
Study Start Date: April 2006
Estimated Study Completion Date: March 2007
Detailed Description:
The purpose of the experiment is to evaluate how coffee affects different individuals while completing computer tasks. If an individual agrees to participate, particpants will be asked to come to the laboratory to drink coffee on 2 days. During each visit, participants will be asked to drink coffee, complete forms, and perform computer tasks. To be eligible to participate, participants must be medically healthy.

Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Participants must be regular coffee drinkers.

For more information or to set up an appointment, please send a contact number (and a convenient time to call) via e-mail and a BPHP laboratory member will contact you or call the BPHP laboratory at the number listed below.

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00336271

United States, District of Columbia
Room 137 Asbury Building-American University
Washington, District of Columbia, United States, 20016-8062
Sponsors and Collaborators
American University
Principal Investigator: Sarah Moore, B.S. American University
Study Director: Laura Juliano, Ph.D. American University
  More Information Identifier: NCT00336271     History of Changes
Other Study ID Numbers: 010
Study First Received: June 9, 2006
Last Updated: March 14, 2007

Keywords provided by American University:
healthy subjects processed this record on August 16, 2017