Actively Recruiting

Age: 9Years - 12Years
All Genders
Healthy Volunteers
NCT04701671

Project THINK: Trajectories of Health, Ingestive Behaviors, and Neurocognition in Kids

Led by University of Pittsburgh · Updated on 2025-12-10

180

Participants Needed

2

Research Sites

386 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

B

Brown University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Overweight/obesity and loss of control eating (characterized by the sense that one cannot control what or how much one is eating) are prevalent among children and adolescents, and both are associated with serious medical and psychosocial health complications. Although our recently published data suggest that youth with these conditions may have relative deficits in neurocognitive functioning, particularly working memory, understanding of how these processes and their neural correlates are related to change and stability in eating and weight-related outcomes over time is limited, thereby impeding development of targeted, optimally timed interventions. The present study aims to assess prospective associations between general and food-specific executive functioning and underlying neural substrates, and eating and weight outcomes among children at varying levels of risk overweight/obesity and eating disorders, which will help guide research efforts towards the development of effective prevention and intervention strategies.

CONDITIONS

Official Title

Project THINK: Trajectories of Health, Ingestive Behaviors, and Neurocognition in Kids

Who Can Participate

Age: 9Years - 12Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Not currently taking any medications known to affect weight or appetite
  • No current or past medical or psychiatric conditions significantly affecting eating or weight except binge eating disorder
  • General intellectual functioning in the low average range or higher
  • No conditions affecting executive functioning such as recent concussion or traumatic brain injury
  • Fluent in English and able to read and understand study materials
  • Not currently pregnant
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

University of PIttsburgh

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

2

Weight Control & Diabetes Research Center

Providence, Rhode Island, United States, 02903

Active, Not Recruiting

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Research Team

E

Erin Stalvey, B.S.

CONTACT

C

Chloe Hudson, B.S.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

6

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