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Formalizing a Conceptual Framework of Work Domain Knowledge

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00882479
First Posted: April 16, 2009
Last Update Posted: June 14, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Min Zhu, The University of Texas Health Science Center, Houston
  Purpose
The purpose of this study is to learn the daily activities of nutrition management software users through an improved informed consent process and develop a conceptual model to describe these activities. The investigators will gather information from nutrition management software users, and design and test a new prototype of nutrition management software.

Condition
Knowledge Representation Knowledge Modeling

Study Type: Observational
Study Design: Time Perspective: Cross-Sectional
Official Title: Formalizing a Conceptual Framework of Work Domain Knowledge

Further study details as provided by Min Zhu, The University of Texas Health Science Center, Houston:

Enrollment: 51
Study Start Date: April 2009
Study Completion Date: June 2011
Primary Completion Date: June 2011 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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, Learn About Clinical Studies.


Ages Eligible for Study:   21 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population

Inclusion Criteria:

  1. Subjects must be over 21 years old
  2. Subjects must be a student or employee in University of Texas
  3. Subjects must be able to read and write in English
  4. Subjects must be able to give signed informed consent
Criteria

Inclusion Criteria:

  1. Subjects must be over 21 years old
  2. Subjects must be a student or employee in University of Texas
  3. Subjects must be able to read and write in English
  4. Subjects must be able to give signed informed consent
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00882479


Locations
United States, Texas
Cognitive Informatics Lab
Houston, Texas, United States, 77030
Sponsors and Collaborators
The University of Texas Health Science Center, Houston
Investigators
Principal Investigator: Min Zhu, MD, MSC UTHSC-Houston
  More Information

Responsible Party: Min Zhu, Program Manager-Research, The University of Texas Health Science Center, Houston
ClinicalTrials.gov Identifier: NCT00882479     History of Changes
Other Study ID Numbers: HSC-SHIS-09-0047
First Submitted: April 14, 2009
First Posted: April 16, 2009
Last Update Posted: June 14, 2012
Last Verified: June 2012