Pennington Generation Cohort
1 other identifier
observational
3,000
1 country
1
Brief Summary
The Pennington Generation Cohort is an observational study comprised of Louisiana families. Families will be assessed at baseline for a variety of traits and behaviors, and then followed up over time to try to understand the role of lifestyle and the environment on the risk of developing obesity and other health outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2025
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 19, 2025
CompletedStudy Start
First participant enrolled
February 24, 2025
CompletedFirst Posted
Study publicly available on registry
February 27, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 24, 2045
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 24, 2045
March 17, 2025
March 1, 2025
20 years
February 19, 2025
March 13, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Obesity
The development of obesity, defined using BMI z-scores during childhood, and BMI during adulthood.
From enrollment up to 20 years of follow-up.
Secondary Outcomes (3)
Weight change
From enrollment up to 20 years of follow-up.
Mortality
From enrollment up to 20 years of follow-up..
Cancer incidence
From enrollment up to 20 years of follow-up..
Eligibility Criteria
Adults of child-bearing age who are planning to become pregnant, expectant parents, as well as children, adolescents, and young adults and their nuclear family members will be recruited.
You may qualify if:
- Children, adolescents, and young adults (birth through age 24 years) and their nuclear family members\* and adults age 25+ who are expectant parents or are trying to conceive
- Self-reported resident of Louisiana
- Ability to understand instructions and complete all study procedures
- Able to provide informed consent (adults aged over 18 years)
- Able to provide assent (children 9 to 17 years)
- Able to communicate (oral and written) in English
You may not qualify if:
- Discretion of the Medical Monitor or Principal Investigator
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Pennington Biomedical Research Center
Baton Rouge, Louisiana, 70808, United States
Biospecimen
Saliva
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Peter T Katzmarzyk, PhD
Pennington Biomedical Research Center
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
February 19, 2025
First Posted
February 27, 2025
Study Start
February 24, 2025
Primary Completion (Estimated)
February 24, 2045
Study Completion (Estimated)
February 24, 2045
Last Updated
March 17, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
- Time Frame
- Data will be made available 1 year after publication of the primary outcomes manuscript.
- Access Criteria
- Upon reasonable request to the principal investigator and in alignment with the goals of the IRB-approved protocol.
A de-identified individual-level dataset will be made available to researchers making a reasonable request to the principal investigator.