Pennington Center Longitudinal Study (PCLS) (PCLS)

July 21, 2023 updated by: Peter T. Katzmarzyk, Pennington Biomedical Research Center

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.

Study Overview

Status

Recruiting

Conditions

Detailed Description

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.

Study Type

Observational

Enrollment (Estimated)

30000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: Peter Katzmarzyk, PhD
  • Phone Number: 225-763-2563
  • Email: doctors@pbrc.edu

Study Locations

  • United States
    • Louisiana
      • Baton Rouge, Louisiana, United States, 70809
        • Recruiting
        • Pennington Biomedical Research Center
        • Principal Investigator:
          • Peter Katzmarzyk, PhD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Community Sample

Description

Inclusion Criteria:

  • 18 years or older
  • volunteer to Participate

Exclusion Criteria:

  • younger than 18 years
  • Pregnant

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.
twenty-years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Pennington Biomedical Research Center

Investigators

  • Principal Investigator: Peter Katzmarzyk, PhD, Associate Executive director for Population Science

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

May 1, 2009

Primary Completion (Estimated)

February 1, 2025

Study Completion (Estimated)

February 1, 2025

Study Registration Dates

First Submitted

August 13, 2009

First Submitted That Met QC Criteria

August 13, 2009

First Posted (Estimated)

August 14, 2009

Study Record Updates

Last Update Posted (Estimated)

July 24, 2023

Last Update Submitted That Met QC Criteria

July 21, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • PBRC 28027

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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