Taste Reward Processing in Pediatric Obesity

This study is currently recruiting participants. (see Contacts and Locations)
Verified September 2013 by Stanford University
Sponsor:
Information provided by (Responsible Party):
Cara Bohon, PhD, Stanford University
ClinicalTrials.gov Identifier:
NCT01908153
First received: July 23, 2013
Last updated: September 24, 2013
Last verified: September 2013
  Purpose

The study aims to provide a better understanding of the neural influence of eating behavior in the development of childhood obesity. Children ages 4-6 will be recruited to examine fMRI brain response to pictures that signal delivery of a chocolate milkshake and to the taste itself. The brain response will be compared to body mass index percentile scores for each child to help us determine whether brain differences present in adolescents and adults with obesity are present in young children.


Condition
Pediatric Obesity

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Taste Reward Processing in Pediatric Obesity

Resource links provided by NLM:


Further study details as provided by Stanford University:

Primary Outcome Measures:
  • fMRI brain response to taste of chocolate milkshake [ Time Frame: Baseline ] [ Designated as safety issue: No ]
  • fMRI brain response to picture cue [ Time Frame: Baseline ] [ Designated as safety issue: No ]

Estimated Enrollment: 30
Study Start Date: September 2013
Estimated Primary Completion Date: September 2014 (Final data collection date for primary outcome measure)
Groups/Cohorts
Overweight/Obese
Children with BMI percentile of 85 or above.
Healthy Weight
Children with BMI percentile between 15 and 85.

  Eligibility

Ages Eligible for Study:   4 Years to 6 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Children ages 4-6

Criteria

Inclusion Criteria:

  • ages 4-6
  • parent available to complete surveys in English

Exclusion Criteria:

  • no presence of metal in body
  • no claustrophobia
  • no psychiatric or neurological condition that will affect brain function
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01908153

Locations
United States, California
Stanford University Department of Psychiatry Recruiting
Stanford, California, United States, 94305
Contact: Natalie Portillo    650-723-7885    nport22@stanford.edu   
Principal Investigator: Cara Bohon, PhD         
Sponsors and Collaborators
Stanford University
Investigators
Principal Investigator: Cara Bohon, PhD Stanford University
  More Information

No publications provided

Responsible Party: Cara Bohon, PhD, Assistant Professor, Stanford University
ClinicalTrials.gov Identifier: NCT01908153     History of Changes
Other Study ID Numbers: UL1 TR000093
Study First Received: July 23, 2013
Last Updated: September 24, 2013
Health Authority: United States: Institutional Review Board

Keywords provided by Stanford University:
Picture food type
Taste type

Additional relevant MeSH terms:
Obesity
Pediatric Obesity
Overnutrition
Nutrition Disorders
Overweight
Body Weight
Signs and Symptoms

ClinicalTrials.gov processed this record on August 27, 2014