Family-based Lifestyle Intervention Program and Carotenoid Supplementation for Children With Obesity
Primary Purpose
Pediatric Obesity
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Lifestyle intervention and carotenoid supplements
Lifestyle intervention and placebo
Sponsored by
About this trial
This is an interventional treatment trial for Pediatric Obesity focused on measuring Obesity, Diabetes Mellitus, Diabetes Mellitus, Type 2, Prevention, Behavioral research, Metabolic Syndrome, Metabolic Disease, Overnutrition, Nutrition Disorders, Overweight, Body weight, Insulin resistance, Carotenoids, Dietary Supplement, Physical fitness, Sedentary lifestyle
Eligibility Criteria
Inclusion Criteria:
- Age 8 years to 11 years at enrollment
- BMI percentile ≥ 95th percentile
Exclusion Criteria:
- Any major chronic diseases, cognitive impairments, or any organic cause of obesity
- any orthopedic or neuromuscular condition that prevents/impedes age-appropriate physical activity
- confirmed diagnosis of Prader-Willi syndrome
- any metal implants that would preclude subject from safely having the MRI procedure
Sites / Locations
- Nemours Children's Clinic
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Lifestyle intervention and carotenoid supplement
Lifestyle intervention and placebo
Arm Description
Outcomes
Primary Outcome Measures
Participation rates, satisfaction with the intervention, responses from the qualitative interview post-intervention, and health and medical outcomes
β-carotene, FABP4 and C16:1n7 palmitolate levels
Secondary Outcome Measures
Macrophage expression of genes involved in lipid and lipoprotein metabolism and adipose deposition
Full Information
NCT ID
NCT02060279
First Posted
April 16, 2013
Last Updated
February 7, 2014
Sponsor
Nemours Children's Clinic
1. Study Identification
Unique Protocol Identification Number
NCT02060279
Brief Title
Family-based Lifestyle Intervention Program and Carotenoid Supplementation for Children With Obesity
Official Title
A 6-month Family-based, Intense Lifestyle Intervention Program and Carotenoid Supplementation for Children With Obesity: A Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
February 2014
Overall Recruitment Status
Completed
Study Start Date
October 2012 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
July 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nemours Children's Clinic
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a pilot study of children between the ages of 8 to 11 years of age who are obese and participating in an intense family based intervention with a family-focused multi-component lifestyle intervention. In addition, a beta-carotene supplement will be administered to randomized participants.
Detailed Description
The spread of childhood obesity across all ethnic and socioeconomic classes in North America is alarming. The close link between morbid obesity and type II diabetes (T2DM) and in childhood is undisputed fact and recent statistics reported by the American Diabetes Association suggest that newly diagnosed cases are on the rise. The link between decreased exercise, increased calorie and fat intake, decrease intake of fruits and vegetables and increased frequency of T2DM are well established. Complications of child obesity include risks for heart disease, high cholesterol, high blood pressure, diabetes, and even some cancers. The lack of fruit and vegetable consumption may be responsible for specific nutrient deficiencies such as low β-carotene, which has recently been identified as an important regulator of body fat. Nemours and Wolfson Children's Hospital have taken the initiative to explore factors that contribute to childhood obesity including well controlled studies examining the effects of intensive nutritional and behavioral education, healthy eating and increased exercise as ways to help prevent the rise in childhood obesity. This study aims to institute an intensive 2 week in-patient intervention which will serve as a model for behavioral changes required in children and families to successfully address the rapid progression of obesity. We will administer a supplement of β-carotene and follow the changes in abdominal fat accumulation over six months. At the third week of intervention we will obtain a blood sample that will determine if any beneficial changes have already taken place in white blood cells that clear cholesterol from the arteries using genetic testing. At the end of the study we will compare the amount of abdominal fat that accumulates or decreases in each subject. An intensive educational program that leads to healthy eating and the habitual exercise for the whole family will help promote significant benefits in the rate of weight gain and delay the progression to diabetes.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pediatric Obesity
Keywords
Obesity, Diabetes Mellitus, Diabetes Mellitus, Type 2, Prevention, Behavioral research, Metabolic Syndrome, Metabolic Disease, Overnutrition, Nutrition Disorders, Overweight, Body weight, Insulin resistance, Carotenoids, Dietary Supplement, Physical fitness, Sedentary lifestyle
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
25 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Lifestyle intervention and carotenoid supplement
Arm Type
Experimental
Arm Title
Lifestyle intervention and placebo
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
Lifestyle intervention and carotenoid supplements
Intervention Description
2 week intervention partial hospitalization program followed by 8 bi-monthly sessions of a lifestyle intervention group run by a psychologist or health coach (research assistant). The entire intervention will last approximately 6 months. Children will participate in all aspects of the intervention including: dietary groups, life coaching, art and music therapy, school based learning, group therapy, physical activity, cooking, preparing meals, family therapy sessions, and yoga. The participants randomized to this study arm will also take Jarrow Formulas CaroteneAll® (5000 IU) supplement while at the intervention site for 2 weeks and then will continue to take the supplements for up to 6 months until their participation in the study is complete. Two capsules of supplement will be consumed daily with a meal with 6 oz. of water.
Intervention Type
Other
Intervention Name(s)
Lifestyle intervention and placebo
Intervention Description
2 week intervention partial hospitalization program followed by 8 bi-monthly sessions of a lifestyle intervention group run by a psychologist or health coach (research assistant). The entire intervention will last approximately 6 months. Children will participate in all aspects of the intervention including: dietary groups, life coaching, art and music therapy, school based learning, group therapy, physical activity, cooking, preparing meals, family therapy sessions, and yoga. The participants randomized to this study arm will also take a gel-cap placebo while at the intervention site for 2 weeks and then will continue to take the placebo for up to 6 months until their participation in the study is complete. Two capsules of placebo will be consumed daily with a meal with 6 oz. of water.
Primary Outcome Measure Information:
Title
Participation rates, satisfaction with the intervention, responses from the qualitative interview post-intervention, and health and medical outcomes
Time Frame
6 months
Title
β-carotene, FABP4 and C16:1n7 palmitolate levels
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Macrophage expression of genes involved in lipid and lipoprotein metabolism and adipose deposition
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
11 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 8 years to 11 years at enrollment
BMI percentile ≥ 95th percentile
Exclusion Criteria:
Any major chronic diseases, cognitive impairments, or any organic cause of obesity
any orthopedic or neuromuscular condition that prevents/impedes age-appropriate physical activity
confirmed diagnosis of Prader-Willi syndrome
any metal implants that would preclude subject from safely having the MRI procedure
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amanda S Lochrie, PhD
Organizational Affiliation
Nemours Children's Clinic
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jose A Canas, MD
Organizational Affiliation
Nemours Children's Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nemours Children's Clinic
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
28323947
Citation
Canas JA, Lochrie A, McGowan AG, Hossain J, Schettino C, Balagopal PB. Effects of Mixed Carotenoids on Adipokines and Abdominal Adiposity in Children: A Pilot Study. J Clin Endocrinol Metab. 2017 Jun 1;102(6):1983-1990. doi: 10.1210/jc.2017-00185.
Results Reference
derived
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Family-based Lifestyle Intervention Program and Carotenoid Supplementation for Children With Obesity
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