Observational study on obesity prevention in Louisiana families

Pennington Generation Cohort

Pennington Biomedical Research Center · NCT06849206

This study follows Louisiana families to see how different habits and programs can help prevent obesity in children over time.

Quick facts

Study typeObservational
Enrollment3000 (estimated)
SexAll
SponsorPennington Biomedical Research Center (other)
Locations1 site (Baton Rouge, Louisiana)
Trial IDNCT06849206 on ClinicalTrials.gov

What this trial studies

The Pennington Generation Cohort is an observational study that follows Louisiana families to assess various traits and behaviors related to obesity prevention. Families will undergo an initial physical exam to establish baseline data on lifestyle, genetics, and body composition. Over time, the study will evaluate the impact of participation in childhood obesity prevention programs on health outcomes. This longitudinal approach includes clinical visits, questionnaires, and potential linkages to health databases for comprehensive follow-up.

Who should consider this trial

Good fit: Ideal candidates include children, adolescents, and young adults up to age 24, along with their families, who are residents of Louisiana.

Not a fit: Patients who do not reside in Louisiana or are outside the specified age range may not benefit from this study.

Why it matters

Potential benefit: If successful, this study could provide valuable insights into effective strategies for preventing obesity in children and adolescents.

How similar studies have performed: Other studies focusing on childhood obesity prevention have shown promise, indicating that this approach may yield beneficial results.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 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

Exclusion Criteria:

* Discretion of the Medical Monitor or Principal Investigator

Where this trial is running

Baton Rouge, Louisiana

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.

View on ClinicalTrials.gov →

Conditions: Obesity Prevention, physical activity, obesity, diet, nutrition, families

Last reviewed 2026-05-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.