Sign in

NCT03254576Completed

Cue-Reward Learning and Weight Gain in Youth

Source: ClinicalTrials.gov · Last updated 29 Jan 2024

Brief summary (registry, in English)

The objective of the study is to compare children at low risk for obesity (two healthy weight parents) to children at high risk for obesity (two overweight parents) in their response rate to food taste and in their rate of learning using fMRI.

Status (registry)
Completed
Study type
Observational
Enrollment
147 (actual)
First submitted
16 Aug 2017
Start date
1 Dec 2016
Primary completion date
27 Dec 2023
Lead sponsor
University of California, San Diego
Diseases
Obesity
NCT number
NCT03254576

What you commit to

  • Study type: Observational
  • Participants enrolled: 147
  • From 1 Dec 2016 to the primary completion date, 27 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Child who is taking medications that may impact brain responses (can take kids who are stable on meds)

Other illness

  • Child diagnoses of a serious chronic physical disease (e.g., diabetes) for which physician supervision of diet and exercise prescription are needed
  • Child with an active eating disorder (reported on EDE interview) or with first degree relative with Anorexia Nervosa or Bulimia Nervosa
  • Cognitive impairment or disability determined through parent and child self-report measures, and parent reported child individual education plan
  • Food allergies related to cheese pizza, chocolate milkshake, or the snack foods used in the study

Other

  • Child overweight (BMI≥85th percentile)
  • Child with MRI contraindications (presence of metallic foreign object or device in body, piercings that cannot be removed, tattooed permanent makeup that contain metal, braces, head trauma, claustrophobia, use of Bigen permanent hair dye)
  • Vision problems uncorrectable with lenses
  • Menarche in female participants at time of enrollment
  • Children scoring within the midpubertal range or higher based on the Pubertal Development Scale

Who the study is looking for

  • Healthy weight children between the ages of 8 and 11 Years
  • BMI 5-75th percentile
  • Child must be right-handed
  • Child must be willing to participate in an fMRI scan
  • Either two biological parents who are overweight/obese or no biological parents that are overweight/obese
  • One biological parent willing to bring child to assessment visits
  • Child and participating parent Fluent in English for speaking, reading, and writing
  • Child must like cheese pizza and chocolate milkshake

Age in the registry: 8 years to 11 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
UCSD Center for Healthy Eating and Activity Research (CHEAR
Coordinator of this site? Confirm its status
La JollaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.