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Brain Activation and Satiety in Children: Functional Magnetic Resonance Imaging (BASIC-FMRI)

Primary Purpose

Childhood Obesity

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Family Based Behavioral Treatment
Sponsored by
Seattle Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Childhood Obesity focused on measuring Family Based Behavioral Treatment, functional magnetic resonance imaging (fMRI), Childhood Obesity, Satiety, BMI z-score, Impulsive, Non-obese controls, Visual food cues, Leptin, Hormones

Eligibility Criteria

9 Years - 11 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 9-11 years of age
  • Male or female
  • Ability and willingness to participate in study visits including fMRI scans and blood draws;
  • ability to provide informed written consent and assent;
  • BMI z-score for lean control children 15th to 84.9th perc. for age and sex,
  • BMI z-score for obese children BMI z-score >90th perc. for age and sex;
  • Additional inclusion criteria for obese children: One overweight parent (BMI >25 kg/m2); willingness of 1 parent (does not have to be the obese parent) to engage in family-based weight control treatment.

Exclusion Criteria:

  • History of acute or chronic serious medical conditions;
  • known diabetes mellitus or recent (6 mo.) history of anemia;
  • presence of any implanted metal or metal devices, including ferro-metallic surgical clips or braces;
  • claustrophobia;
  • documented cognitive disorder, disruptive behavior, inability to participate in group sessions;
  • current use of medications known to alter appetite, body weight, or brain response (e.g. anti-seizure medications, glucocorticoids, medications for attention deficit disorder);
  • food intolerance or vegetarianism.

Sites / Locations

  • Seattle Childrens Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Family Based Behavioral Treatment

Arm Description

Central satiety brain and hormonal responses will be compared pre-and post-Family Based Behavioral Treatment, as well, as to a non-obese sample.

Outcomes

Primary Outcome Measures

Blunted central satiety response measured by functional magnetic resonance imaging

Secondary Outcome Measures

Change of brain response to visual food cues or eating behavior measured by functional magnetic resonance imaging
Relationship between impulsivity and satiety in obese children as measured by functional magnetic resonance imaging.
Relationship between impulsivity and satiety in obese children as measured by the Relative Reinforcing Value of Food (RRV).
Relationship between impulsivity and satiety in obese children as measured by the Developmental NEuroPSYchological Assessment (NEPSY).
Relationship between impulsivity and satiety in obese children as measured by the Delayed Choice Questionnaire (DCQ).

Full Information

First Posted
November 20, 2014
Last Updated
September 5, 2018
Sponsor
Seattle Children's Hospital
Collaborators
University of Washington
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1. Study Identification

Unique Protocol Identification Number
NCT02484976
Brief Title
Brain Activation and Satiety in Children: Functional Magnetic Resonance Imaging
Acronym
BASIC-FMRI
Official Title
Brain Systems and Behaviors Underlying Response to Obesity Treatment in Children
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
September 2014 (undefined)
Primary Completion Date
July 2018 (Actual)
Study Completion Date
August 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seattle Children's Hospital
Collaborators
University of Washington

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
BASIC fMRI is a prospective single center intervention trial using fMRI imaging in 9-11 year old obese male and females pre and post family-based behavioral treatment of 24 weeks duration to determine the relationship between impulsivity and central satiety responses.
Detailed Description
The high prevalence of childhood obesity in the U.S. demands a better understanding of factors that drive weight gain and influence the outcome of pediatric obesity interventions. This project investigates the hypothesis that, as in adults, a subset of obese children experience a diminished satiety response to food consumption, and that these children are more resistant to gold standard family-based behavioral treatment (FBT) for obesity. FBT is targeted almost exclusively toward parents; however, there is evidence that obesity development and response to intervention may depend on additional factors such as individual internal satiety perception and variability in the function of brain centers associated with impulsivity and reward. The proposed research uses functional magnetic resonance imaging (fMRI) to characterize brain function related to satiety and examines fMRI along with behavioral, cognitive, and hormonal testing to fully examine potential mediators of children's experience of satiety and response to FBT. The approach is based on evidence that failure to attenuate the reward value of palatable foods after eating can be a manifestation of a blunted central satiety response that is reliably detected using fMRI. Key objectives will be to determine if differences in the central satiety response exist between obese and non-obese children, and, among obese children, if the strength of the central satiety response is associated with impulsivity and/or the success of obesity treatment. The central hypothesis is that, in obese children, a blunted central nervous system satiety response impairs the success of obesity interventions. To achieve study objectives, brain activation by high-calorie visual food cues before and after food consumption will be measured by fMRI. Participants will be obese and non-obese children aged 9-11 years. The 49 obese children will be evaluated before and after they participate in a 6-month evidence-based FBT intervention. Their pre-intervention fMRI will be compared to those of 20 non-obese controls to test for a blunted central satiety response (Aim 1). The relationship of impulsivity to satiety responses and food intake will be determined in obese children (Aim 2). The longitudinal component tests whether central satiety responses prior to treatment predict treatment outcomes (Aim 3A) and whether changes in central satiety responses during treatment predict maintenance of reduced weight 6 and 12 months after treatment cessation (Aim 3B). Behavioral, cognitive, and hormonal measures will be examined as potential mediating or confounding factors contributing to fMRI responses. The proposed research is guided by an integrated, transdisciplinary team with expertise in pediatric and adult neuroimaging, appetite regulation, and family-based childhood obesity treatment. This research will provide new insights into the neurobiological basis of child obesity and the relevance of neurobiological factors to treatment success. The long-term objective is to translate these findings to improve obesity interventions cost-effectively and sustain better long-term results. During years 1-3, obese children will be enrolled into intervention groups of 9-11 families with staggered start dates by 3-6 months. Years 1-4 includes enrollment, intervention, longitudinal follow-up, and data collection for obese children. Control children will primarily be recruited during years 2-3 to facilitate matching. FMRI scans are processed on a rolling basis as studies are completed. In years 3 and 4 hormonal assays will be performed. Final data analyses will be completed in year 4.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Childhood Obesity
Keywords
Family Based Behavioral Treatment, functional magnetic resonance imaging (fMRI), Childhood Obesity, Satiety, BMI z-score, Impulsive, Non-obese controls, Visual food cues, Leptin, Hormones

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
81 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Family Based Behavioral Treatment
Arm Type
Experimental
Arm Description
Central satiety brain and hormonal responses will be compared pre-and post-Family Based Behavioral Treatment, as well, as to a non-obese sample.
Intervention Type
Behavioral
Intervention Name(s)
Family Based Behavioral Treatment
Intervention Description
Obese children accompanied by at least one parent or caregiver will attend 24 weekly in-person sessions. Sessions will include 25-30 min. meetings between an interventionist and each child/parent pair to individualize treatment, followed by separate child and parent group meetings lasting 40 - 45 min. Parents will serve as primary agents of change for their child and for themselves. Training will focus on food and physical activity education, parenting around food and physical activity, and use of behavioral skills (e.g., self-monitoring, environmental control, contingency management). Intervention groups of 9-11 children/families will be initiated every 3-6 mos. in study yrs. 1-3.
Primary Outcome Measure Information:
Title
Blunted central satiety response measured by functional magnetic resonance imaging
Time Frame
Baseline
Secondary Outcome Measure Information:
Title
Change of brain response to visual food cues or eating behavior measured by functional magnetic resonance imaging
Time Frame
Change from pre- to post-treatment (end of 6 month intervention)
Title
Relationship between impulsivity and satiety in obese children as measured by functional magnetic resonance imaging.
Time Frame
Change from pre- to post-treatment (end of 6 month intervention)
Title
Relationship between impulsivity and satiety in obese children as measured by the Relative Reinforcing Value of Food (RRV).
Time Frame
Change from pre- to post-treatment (end of 6 month intervention)
Title
Relationship between impulsivity and satiety in obese children as measured by the Developmental NEuroPSYchological Assessment (NEPSY).
Time Frame
Change from pre- to post-treatment (end of 6 month intervention)
Title
Relationship between impulsivity and satiety in obese children as measured by the Delayed Choice Questionnaire (DCQ).
Time Frame
Change from pre- to post-treatment (end of 6 month intervention)
Other Pre-specified Outcome Measures:
Title
Predictors of treatment outcomes measured by functional magnetic resonance imaging.
Time Frame
Change from pre- to post-treatment (end of 6 month intervention)
Title
Predictors of treatment outcomes measured by behavioral skills use questionnaires.
Time Frame
Change from pre- to post-treatment (end of 6 month intervention)
Title
Predictors of treatment outcomes measured by hormonal measures.
Time Frame
Change from pre- to post-treatment (end of 6 month intervention)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
9 Years
Maximum Age & Unit of Time
11 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 9-11 years of age Male or female Ability and willingness to participate in study visits including fMRI scans and blood draws; ability to provide informed written consent and assent; BMI z-score for lean control children 15th to 84.9th perc. for age and sex, BMI z-score for obese children BMI z-score >90th perc. for age and sex; Additional inclusion criteria for obese children: One overweight parent (BMI >25 kg/m2); willingness of 1 parent (does not have to be the obese parent) to engage in family-based weight control treatment. Exclusion Criteria: History of acute or chronic serious medical conditions; known diabetes mellitus or recent (6 mo.) history of anemia; presence of any implanted metal or metal devices, including ferro-metallic surgical clips or braces; claustrophobia; documented cognitive disorder, disruptive behavior, inability to participate in group sessions; current use of medications known to alter appetite, body weight, or brain response (e.g. anti-seizure medications, glucocorticoids, medications for attention deficit disorder); food intolerance or vegetarianism.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christian Roth, MD
Organizational Affiliation
Seattle Children's
Official's Role
Principal Investigator
Facility Information:
Facility Name
Seattle Childrens Hospital
City
Seattle
State/Province
Washington
ZIP/Postal Code
89105
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34357785
Citation
Saelens BE, Melhorn SJ, Rowland MG, Scholz K, De Leon MRB, Elfers CT, Schur EA, Roth CL. General and Food-Specific Impulsivity and Inhibition Related to Weight Management. Child Obes. 2022 Mar;18(2):84-91. doi: 10.1089/chi.2021.0080. Epub 2021 Aug 5.
Results Reference
derived
PubMed Identifier
30418574
Citation
Roth CL, Melhorn SJ, Elfers CT, Scholz K, De Leon MRB, Rowland M, Kearns S, Aylward E, Grabowski TJ, Saelens BE, Schur EA. Central Nervous System and Peripheral Hormone Responses to a Meal in Children. J Clin Endocrinol Metab. 2019 May 1;104(5):1471-1483. doi: 10.1210/jc.2018-01525.
Results Reference
derived

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Brain Activation and Satiety in Children: Functional Magnetic Resonance Imaging

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