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Metabolic Optimization Through Diet/Lifestyle Improvements For Youth (MODIFY)

Primary Purpose

Dyslipidemias, Obesity

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Alive-Family
Sponsored by
Children's National Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dyslipidemias focused on measuring cardiometabolic risk factors, lifestyle modification, visceral adiposity

Eligibility Criteria

10 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Adolescent inclusion criteria:

Aged 10 years to 18 years Dyslipidemia (TG/HDL-c >2.5 in non-Black males and >2.0 in females and Black males) Central adiposity (waist to height ratio > 0.5) Willingness to participate

Adult inclusion criteria:

Parent or adult caregiver of adolescent patient Central adiposity (waist to height ratio >0.5) Willingness to participate

Exclusion criteria (adolescent and parent) include

  • Diabetes, genetic syndrome, stage II hypertension (systolic or diastolic BP > 95th percentile for age, sex, and height percentile + 12mm Hg or > 140/90, whichever is lower for subjects < 13 yr of age, > 140/90 for all > 13 yr of age, including PAC; history of hypertension controlled on stable medication regimen accepted)
  • Medication use known to affect insulin sensitivity or lipid profiles, including metformin, statins, fibric acids or second generation atypical anti-psychotics (stable doses of stimulant or antidepressant therapy accepted)
  • Current participation and unwillingness to cease activities related to a diet/exercise lifestyle modification program other than this program
  • Any medical condition or syndrome with neurocognitive delay that would preclude active participation with the mobile health app
  • Pregnancy or intention to become pregnant (as this will alter weight distribution)
  • Inability to participate in moderate physical activity

Sites / Locations

  • Childrens National Hospital

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Treatment

Arm Description

Participants will be asked use a mobile health (m-health) app for 2 months. The app is designed to provide weekly education and motivation about healthful diet and physical activity behaviors in adolescents and their parent/adult caretaker. Both adolescent and parent/adult caretaker participants will use the app to enter weekly self-report data, set healthy eating and exercise goals, and receive educational and motivational content. Participants will conduct a weekly self-assessment of waist circumference, diet, and physical activity during the 2 month trial.

Outcomes

Primary Outcome Measures

Change in plasma ceramides
S1P, C:14, and C:16

Secondary Outcome Measures

Change in plasma lipids
Plasma triglycerides, HDL-c, LDL-c
Change in plasma glucose
Change in plasma insulin
Change in plasma C-reactive protein (CRP)
Change in waist circumference
Change in BMI
weight for height (Kg/M^2)
Change in physical activity
Physical activity is assessed by self-report questionnaire. The activity questionnaire asks about frequency and duration of performance of a list of activities.
Change in diet
Diet assessment by food frequency questionnaire (FFQ) to determine quantity and quality of macronutrients (carbs, protein, fat) and food groups (i.e. sugar sweetened beverages, fruits, vegetables, etc.) indexed as healthy eating score (Alternative Healthy Eating Index) on a scale of 2.5 to 87.5 with a higher score reflecting a more healthful diet.

Full Information

First Posted
February 11, 2020
Last Updated
February 3, 2022
Sponsor
Children's National Research Institute
Collaborators
University of California, Davis, NutritionQuest
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1. Study Identification

Unique Protocol Identification Number
NCT04270084
Brief Title
Metabolic Optimization Through Diet/Lifestyle Improvements For Youth
Acronym
MODIFY
Official Title
Metabolic Optimization Through Diet/Lifestyle Improvements For Youth (MODIFY)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
September 29, 2020 (Actual)
Primary Completion Date
January 19, 2022 (Actual)
Study Completion Date
December 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's National Research Institute
Collaborators
University of California, Davis, NutritionQuest

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The overarching goal of this study is to evaluate plasma ceramides (Cers) as early nutrition-sensitive biomarkers of metabolic health. The investigators will implement a diet and lifestyle intervention to improve cardiometabolic risk factors and test the corresponding change in Cer levels. The intervention will incorporate: a) family-level engagement, enrolling both adolescents and one parent/adult caretaker (PAC); and b) a behavior change mobile health (m-health) app, which will offer real-time support, education and monitoring of diet and activity.
Detailed Description
Dysregulated sphingolipid ceramide (Cer) metabolism impairs mitochondrial function, insulin sensitivity and vascular reactivity and has been identified as a central common pathway towards the dyslipidemia, central adiposity, hyperglycemia, and hypertension that define metabolic syndrome, characterized as cardiometabolic risk (CMR). The decrease in insulin sensitivity that occurs with age and predisposes to metabolic syndrome is preventable, a reflection of changes in body composition rather than the aging process itself. Ectopic fat, not fat mass per se, drives CMR, but despite mounting concern about rising prevalence of pediatric CMR in America and globally, the use of plasma Cer as potentially mechanistic biomarkers of ectopic fat and lipotoxicity has not been well explored. This may be driven in part by our incomplete understanding of i) the consequences of Cer dysregulation in pediatric CMR; ii) putative interactions between Cer and ectopic lipotoxicity; and iii) how lifestyle, notably nutrition, impacts Cer metabolism. Information in these areas may support use of plasma Cers as sensitive, prognostic biomarkers to guide more effective preventive lifestyle management of aberrant weight gain and associated CMR. In preliminary work, the investigators compared plasma sphingolipid profiles in obese adolescents and their parent/adult caretakers (PAC). Data from this study demonstrated that Cers (notably C:14 and C:16) are associated with dyslipidemia in both adults and youth. The investigators also found that 2-mo of a daily nutrient bar supplementation (coupled with weekly group counseling and exercise) significantly decreased plasma Cers more effectively than counseling and physical exercise alone, without change in traditional biomarkers but the extent of Cer reduction correlated with improved dyslipidemia. The investigators also found that 10 days of dietary fructose reduction in obese pre-adolescents significantly lowers cers in direct proportion to the clearance of ectopic hepatic adiposity. If study hypotheses are supported, these findings will identify sensitive Cer biomarkers of CMR with putative mechanistic insight to mitochondrial function requisite for insulin sensitivity, metabolic flexibility, lipolysis, and weight loss, that might therefore be used to monitor early success in lifestyle change trials.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dyslipidemias, Obesity
Keywords
cardiometabolic risk factors, lifestyle modification, visceral adiposity

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Other
Arm Description
Participants will be asked use a mobile health (m-health) app for 2 months. The app is designed to provide weekly education and motivation about healthful diet and physical activity behaviors in adolescents and their parent/adult caretaker. Both adolescent and parent/adult caretaker participants will use the app to enter weekly self-report data, set healthy eating and exercise goals, and receive educational and motivational content. Participants will conduct a weekly self-assessment of waist circumference, diet, and physical activity during the 2 month trial.
Intervention Type
Behavioral
Intervention Name(s)
Alive-Family
Intervention Description
All participants receive lifestyle modification through use of m-health app
Primary Outcome Measure Information:
Title
Change in plasma ceramides
Description
S1P, C:14, and C:16
Time Frame
Change from Baseline level of plasma ceramides at 2 months
Secondary Outcome Measure Information:
Title
Change in plasma lipids
Description
Plasma triglycerides, HDL-c, LDL-c
Time Frame
Change from Baseline level at 2 months
Title
Change in plasma glucose
Time Frame
Change from Baseline level at 2 months
Title
Change in plasma insulin
Time Frame
Change from Baseline level at 2 months
Title
Change in plasma C-reactive protein (CRP)
Time Frame
Change from Baseline level at 2 months
Title
Change in waist circumference
Time Frame
Change from Baseline level at 2 months
Title
Change in BMI
Description
weight for height (Kg/M^2)
Time Frame
Change from Baseline level at 2 months
Title
Change in physical activity
Description
Physical activity is assessed by self-report questionnaire. The activity questionnaire asks about frequency and duration of performance of a list of activities.
Time Frame
Change from Baseline level at 2 months
Title
Change in diet
Description
Diet assessment by food frequency questionnaire (FFQ) to determine quantity and quality of macronutrients (carbs, protein, fat) and food groups (i.e. sugar sweetened beverages, fruits, vegetables, etc.) indexed as healthy eating score (Alternative Healthy Eating Index) on a scale of 2.5 to 87.5 with a higher score reflecting a more healthful diet.
Time Frame
Change from Baseline level at 2 months
Other Pre-specified Outcome Measures:
Title
Mental health
Description
Mood and outlook will be assessed by self-report questionnaire: Patient Health Questionnaire for somatic symptoms, anxiety, and depression (PHQ-SADS) a continuous scale (0-86) with higher scores reflecting poorer mental health.
Time Frame
Change from Baseline level at 2 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Adolescent inclusion criteria: Aged 10 years to 18 years Dyslipidemia (TG/HDL-c >2.5 in non-Black males and >2.0 in females and Black males) Central adiposity (waist to height ratio > 0.5) Willingness to participate Adult inclusion criteria: Parent or adult caregiver of adolescent patient Central adiposity (waist to height ratio >0.5) Willingness to participate Exclusion criteria (adolescent and parent) include Diabetes, genetic syndrome, stage II hypertension (systolic or diastolic BP > 95th percentile for age, sex, and height percentile + 12mm Hg or > 140/90, whichever is lower for subjects < 13 yr of age, > 140/90 for all > 13 yr of age, including PAC; history of hypertension controlled on stable medication regimen accepted) Medication use known to affect insulin sensitivity or lipid profiles, including metformin, statins, fibric acids or second generation atypical anti-psychotics (stable doses of stimulant or antidepressant therapy accepted) Current participation and unwillingness to cease activities related to a diet/exercise lifestyle modification program other than this program Any medical condition or syndrome with neurocognitive delay that would preclude active participation with the mobile health app Pregnancy or intention to become pregnant (as this will alter weight distribution) Inability to participate in moderate physical activity
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michele Mietus-Snyder, MD
Organizational Affiliation
Children's National Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Childrens National Hospital
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20010
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Metabolic Optimization Through Diet/Lifestyle Improvements For Youth

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