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Recruiting NCT07229508

Developmental Trajectories of Reinforcer Pathology and Childhood Obesity

Observational Pediatric Obesity

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Pediatric Obesity. Basic parameters: 8 years — 11 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Trajectories of Reinforcement, Activity, and Consumption in Kids

Overview

The goal of this observational study is to understand how children's food preferences, physical activity, and decision-making change over time and how these behaviors relate to body weight and overall health.

Detailed description

A cohort sequential design will be used to track 2 cohorts of children aged 8.5-9 years 11 months, and 10.5-11 years 11 months over a 3 year period to understand how the development of food and activity reinforcement and delay discounting could lead to the development of childhood obesity in children aged 9-14.

Primary outcome measures

  • zBMI [Time frame: 0, 12, 24 and 36 months]
  • body fat [Time frame: 0, 12, 24 and 36 months]
  • percent change over the overweight BMI [Time frame: 0, 12, 24 and 36 months]

Eligibility criteria

Inclusion criteria

  • Male and female children
  • Black, Indigenous, and People of Color (BIPOC) or Hispanic families
  • Children from low SES families (as defined by household education, eligibility for government assistance)
  • Children in overweight/obese category (defined by range in each cohort)

Exclusion criteria

  • Medical causes for obesity
  • Stature below the 5th percentile
  • Physical activity restrictions
  • Psychopathology
  • Medication use that affects activity or appetite
  • Children that spend less than 65% of their time in participating parent's household
  • BMI percentile criteria
  • Liking of study foods and activities
  • Dietary restrictions and food allergies

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • State University of New York at Buffalo — Buffalo

Identifiers

NCT: NCT07229508 · STUDY00008702 · 1R01DK139258-01A1

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗