NCT06849206

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
3,000

participants targeted

Target at P75+ for all trials

Timeline
229mo left

Started Feb 2025

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress6%
Feb 2025Feb 2045

First Submitted

Initial submission to the registry

February 19, 2025

Completed
5 days until next milestone

Study Start

First participant enrolled

February 24, 2025

Completed
3 days until next milestone

First Posted

Study publicly available on registry

February 27, 2025

Completed
20 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 24, 2045

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 24, 2045

Last Updated

March 17, 2025

Status Verified

March 1, 2025

Enrollment Period

20 years

First QC Date

February 19, 2025

Last Update Submit

March 13, 2025

Conditions

Keywords

physical activityobesitydietnutritionfamilies

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

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

Saliva

MeSH Terms

Conditions

Motor ActivityObesity

Condition Hierarchy (Ancestors)

BehaviorOverweightOvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Peter T Katzmarzyk, PhD

    Pennington Biomedical Research Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Peter T Katzmarzyk, PhD

CONTACT

Kara Denstel, PhD

CONTACT

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

A de-identified individual-level dataset will be made available to researchers making a reasonable request to the principal investigator.

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.

Locations