MedPath

Brain Activation and Satiety in Children 2

Phase 3
Active, not recruiting
Conditions
Childhood Obesity
Interventions
Behavioral: Family Based Behavioral Treatment
Drug: Placebo
Registration Number
NCT04520490
Lead Sponsor
Seattle Children's Hospital
Brief Summary

Childhood obesity and related long-term effects are serious public health problems, but not all children with obesity do well in treatment. This study will test a new combination of family-based behavioral treatment (FBT) with a drug intervention using a glucagon-like peptide-1 receptor agonist (GLP-1RA) exenatide once weekly extended-release (ExQW, Bydureon®) in order to improve obesity intervention outcomes in 10-12-year-old children.

Detailed Description

Using functional and structural magnetic resonance neuroimaging, this study will evaluate brain factors which could undermine treatment responses and long-term obesity intervention outcomes. Specific Aim 1 will test the effect of adding ExQW to FBT on change in BMI z-score over a total GLP-1RA treatment duration of 24 weeks and a subsequent 1-year observational follow-up period after treatment cessation. To provide mechanistic insight, Specific Aim 2 will test whether adding GLP-1RA intervention to FBT impacts neural activation by food cues. Finally, the proposed research will investigate the role of a cellular inflammatory process in the mediobasal hypothalamus-called gliosis-which might contribute to impaired hypothalamic function, attenuated satiety responsiveness, and potentially to worse weight management outcomes. Specific Aim 3 will test if hypothalamic gliosis is modified by FBT and/or FBT plus GLP-1RA in children and if its extent is related to immediate and/or long-term intervention outcomes.

Study Design: This double-blinded, randomized, placebo-controlled research study uses fMRI to characterize neural responses to a test meal before and at the end of FBT intervention, with vs. without additional GLP-1RA intervention. In addition, it uses structural MRI (sMRI) to test if MBH gliosis is reversible and/or associated with intervention outcomes.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
63
Inclusion Criteria
  • 10-12 years of age
  • Male or female
  • Ability and willingness to participate in study visits including fMRI scans, blood draws, and weekly injections;
  • Parent willing to provide informed written consent and child willing to provide written assent;
  • Child has BMI z-score >95th percentile. for age and sex;
  • One parent that is obese or overweight (BMI >27 kg/m2); willingness of 1 parent (does not have to be the parent with obesity) to engage in weekly family-based weight control treatment delivered in English.
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 orthodontic 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
  • Food intolerance to test meal (macaroni and cheese) or vegetarianism/veganism or severe food allergies.
  • Known renal impairment (GFR<60 ml/min/1.73m2)
  • History of gastroparesis, pancreatitis or gallstones (unless status post cholecystectomy);
  • Family history of multiple endocrine neoplasia type 2 or familial medullary thyroid carcinoma;
  • Known elevated calcitonin level at phone screening or increased measured calcitonin level at study visits;
  • Untreated thyroid disorder or adrenal insufficiency;
  • Use of weight loss medications (child participant) within 3 months of screening visit.
  • Participating parent is pregnant

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Exenatide once weekly extended-releaseExenatide 2 mg [Bydureon]Weekly subcutaneous injections of glucagon-like peptide (GLP)-1 agonist exenatide once weekly extended-release (2mg) for 24 weeks in randomized intervention.
Matching placeboPlaceboWeekly subcutaneous injections of placebo for 24 weeks.
Exenatide once weekly extended-releaseFamily Based Behavioral TreatmentWeekly subcutaneous injections of glucagon-like peptide (GLP)-1 agonist exenatide once weekly extended-release (2mg) for 24 weeks in randomized intervention.
Matching placeboFamily Based Behavioral TreatmentWeekly subcutaneous injections of placebo for 24 weeks.
Primary Outcome Measures
NameTimeMethod
Change of BMI z-scoreChange from drug treatment randomization at week 8 of family-based behavioral treatment (FBT) to end of combined intervention (FBT + drug) at week 24 of FBT

Body mass index (BMI) z-scores will be derived using CDC growth charts, using the LMS method, to allow for comparison of adiposity over time and across children who differ in age and sex.

Secondary Outcome Measures
NameTimeMethod
Meal induced chances in brain activation to visual food cuesChange from Baseline to post-Family Based Behavioral Treatment at week 24

Change of brain response to visual food cues measured by functional magnetic resonance imaging in a priori regions of interest

BMI z-scoreUp to 12-months after ending treatment

Change of body mass index (BMI) z-scores derived using CDC growth charts, using the LMS method, to allow for comparison of adiposity over time and across children who differ in age and sex.

Indices of metabolic syndromeChange from Baseline to post-Family Based Behavioral Treatment at week 24

Changes of insulin resistance assessed by fasting insulin used for homeostasis model assessment of insulin resistance (HOMA-IR) using the formula insulin \[mU/l\] x glucose \[mmol/l\]) / 22.5

Body compositionChange from Baseline to post-Family Based Behavioral Treatment at week 24 and post drug-treatment at week 32

Changes in body composition as assessed using a bioelectrical impedance (BIA)

Trial Locations

Locations (1)

Seattle Children's Hospital

🇺🇸

Seattle, Washington, United States

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