We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Pennington Center Longitudinal Study (PCLS) (PCLS)

This study is currently recruiting participants.
Verified November 2017 by Peter T. Katzmarzyk, Pennington Biomedical Research Center
Sponsor:
ClinicalTrials.gov Identifier:
NCT00959270
First Posted: August 14, 2009
Last Update Posted: November 14, 2017
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. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Information provided by (Responsible Party):
Peter T. Katzmarzyk, Pennington Biomedical Research Center
August 13, 2009
August 14, 2009
November 14, 2017
May 2009
February 2020   (Final data collection date for primary outcome measure)
Cross-sectional analyses database [ Time Frame: twenty-years ]
The only protocol specific to the PCLS study is the collection of blood sample for risk factor determination and storage in the PBRC archive bank, only to be invoked in cases where studies do not include a blood draw as part of their protocol. The PCLS represents an effort to utilize a data collection over the last twenty years during the clinical research studies for cross-sectional analyses, as well as followed prospectively for the development of a variety of health-related outcomes.
Not Provided
Complete list of historical versions of study NCT00959270 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Pennington Center Longitudinal Study (PCLS)
Pennington Center Longitudinal (PCLS)
The purpose of this study is to develop a cohort of volunteers that can be studied and followed up into the future for changes in health behaviors and development of health problems.
The PCLS represents an effort to utilize the data collected over the last twenty years during the clinical research studies conducted at Pennington Biomedical Research Center. A cohort will be developed and used for cross-sectional analyses, as well as followed prospectively for the development of a variety of health-related outcomes. Several data sources from the PBRC clinical database will be used to establish the PCLS database, including screening, archive and study-specific data. The only protocol specific to the PCLS study is the collection of blood sample for risk factor determination and storage in the PBRC archive bank, only to be invoked in cases where studies do not include a blood draw as part of their protocol.
Observational
Observational Model: Cohort
Time Perspective: Cross-Sectional
Not Provided
Retention:   Samples With DNA
Description:
Serum, plasma, buffy coat, whole blood
Probability Sample
Community Sample
  • Health Behaviors
  • Development of Health Problems
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
30000
February 2020
February 2020   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • 18 years or older
  • volunteer to Participate

Exclusion Criteria:

  • younger than 18 years
  • Pregnant
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
Yes
Contact: Peter Katzmarzyk, PhD 225-763-2563 doctors@pbrc.edu
United States
 
 
NCT00959270
PBRC 28027
No
Not Provided
Not Provided
Peter T. Katzmarzyk, Pennington Biomedical Research Center
Pennington Biomedical Research Center
Not Provided
Principal Investigator: Peter Katzmarzyk, PhD Associate Executive director for Population Science
Pennington Biomedical Research Center
November 2017