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Sedentary Behavior in African Americans (SeBA)

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ClinicalTrials.gov Identifier: NCT00907465
Recruitment Status : Completed
First Posted : May 22, 2009
Last Update Posted : December 4, 2012
Sponsor:
Information provided by (Responsible Party):
Robert Newton, Pennington Biomedical Research Center

Brief Summary:
The study is designed to develop methods for objectively measuring sedentary behavior, assess the association between objectively measured sedentary behavior and cardiovascular disease outcomes, and develop an intervention to reduce sedentary behavior, in African American adults.

Condition or disease
Cardiovascular Disease

Study Type : Observational
Actual Enrollment : 25 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Measurement of Sedentary Behavior in African American Adults
Study Start Date : July 2007
Actual Primary Completion Date : October 2008
Actual Study Completion Date : October 2008

Resource links provided by the National Library of Medicine


Group/Cohort
Calibration study
These individuals were used to develop cut points for sedentary behavior using accelerometers and a metabolic chamber.



Primary Outcome Measures :
  1. Sedentary behavior [ Time Frame: 2009-2010 ]

Secondary Outcome Measures :
  1. Blood pressure [ Time Frame: 2009-2010 ]
  2. High density lipoproteins [ Time Frame: 2009-2010 ]


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Community members of Baton Rouge, LA.
Criteria

Inclusion Criteria:

  • self-classify yourself as African American
  • are aged 18 years or older
  • are free of serious medical condition, such as cancer, cardiovascular disease, or emphysema.
  • are free of serious medical conditions that would prevent participant from engaging in physical activity.
  • are willing to have a scan completed that measures your body composition
  • are willing to stay in metabolic chamber for 8.5 hours (8:00am until 4:30 pm)
  • are willing to wear an accelerometer for 2, one-week periods following your chamber stay. There will be one week in-between the 2, one-week periods.
  • are willing to complete questionnaire related to your level of activity
  • weigh less than 250 lbs.

Exclusion Criteria:

  • unwilling or unable to perform activities in protocol
  • on medications
  • a woman who is intending to become pregnant, or who is pregnant

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): NCT00907465


Locations
United States, Louisiana
Pennington Biomedical Research Center
Baton Rouge, Louisiana, United States, 70808
Sponsors and Collaborators
Pennington Biomedical Research Center
Investigators
Principal Investigator: Robert L Newton, Ph.D. Pennington Biomedical Research Center

Responsible Party: Robert Newton, Principal Investigator, Pennington Biomedical Research Center
ClinicalTrials.gov Identifier: NCT00907465     History of Changes
Other Study ID Numbers: PBRC 27013
1K01HL088723-01 ( U.S. NIH Grant/Contract )
First Posted: May 22, 2009    Key Record Dates
Last Update Posted: December 4, 2012
Last Verified: December 2012

Additional relevant MeSH terms:
Cardiovascular Diseases