TIGER Kids: Translational Investigation of Growth and Everyday Routines in Kids

Sponsor
Pennington Biomedical Research Center (Other)
Overall Status
Completed
CT.gov ID
NCT02784509
Collaborator
USDA Beltsville Human Nutrition Research Center (U.S. Fed)
342
1
51
6.7

Study Details

Study Description

Brief Summary

The purpose of this study is to determine the effect of severe obesity on physical activity, sedentary behavior and cardiometabolic risk factors during childhood and adolescence and whether these associations are modified by race. Additionally, the study will investigate the contributions of (total, regional, and depot-specific) fat accumulation on changes in physical activity, sedentary behavior, and cardiometabolic risk factors during childhood and adolescence.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The proposed study will establish a prospective pediatric cohort to identify intervention targets based on the location, timing, barriers, and facilitators of current physical activity and sedentary behavior in a child's day. The project will be a prospective examination of 340 African American and White girls and boys aged 10 to 16 years, including 50% who are classified as severely obese. State-of-the-art technology will be used including accelerometry to quantify physical activity, magnetic resonance imaging to quantify fat accumulation, and geographic position system and ecological momentary assessment to identify environmental and socio-emotional barriers and facilitators. In further detail, this study will examine the following objectives:

    Objective 1: Determine the effect of severe obesity on physical activity, sedentary behavior, and cardiometabolic risk factors during childhood and adolescence and whether these associations are modified by race.

    Objective 2: Investigate the contribution of (total, regional, and depot-specific) fat accumulation on changes in physical activity, sedentary behavior, and cardiometabolic risk factors during childhood and adolescence.

    Objective 3: Determine barriers and facilitators of physical activity that are related to obesity, including environmental and socio-emotional factors.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    342 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Translational Investigation of Growth and Everyday Routines in Kids (TIGER Kids)
    Actual Study Start Date :
    Jun 1, 2016
    Actual Primary Completion Date :
    Sep 1, 2020
    Actual Study Completion Date :
    Sep 1, 2020

    Outcome Measures

    Primary Outcome Measures

    1. Objective 1 Primary Outcome: Change in minutes of sedentary behavior [Year 0 and Year 2]

      Physical activity and sedentary behavior will be measured by a triaxial accelerometer (Actigraph GT3X+, Actigraph of Ft. Walton Beach, FL). The participant will be instructed to wear the accelerometer on an elasticized belt, on the left mid-axillary line. The Actigraph is one of the most common accelerometers used for scientific purposes. Participants will be encouraged to wear the accelerometer 24-hours per day for at least 7-days (plus an initial familiarization day and the morning of the final day), including 2 weekend days. Participants will also complete a Lifestyle survey to collect information including diet and physical activity habits.

    2. Objective 2 Primary Outcome: Relationship between total fat accumulation and change in sedentary behavior. [Year 0 and Year 2]

      Body composition will be determined by DXA and MRI. With DXA, total body fat and trunk fat will be measured by whole-body DXA using a GE iDXA scanner (GE Medical Systems, Milwaukee, WI) to quantify total and regional body fat (including trunk fat). MRI - Visceral fat, i.e. visceral adipose tissue, will be measured by water-fat shifting MRI using the General Electric Discovery 750w 3.0 Tesla (GE Medical Systems, Milwaukee, WI). IDEAL-IQ imaging technique will be used to generate water-only, fat-only, in-phase, and out-of-phase echoes in a single acquisition with a 20-second breath-hold. Sedentary behavior will be measured by a a triaxial accelerometer as described in outcome 1. Participants will also complete a Lifestyle survey to collect information including physical activity habits.

    3. Objective 3 Primary Outcome: Relationship between BMIz and the environmental (or socio-emotional) factors. [Year 0 and Year 2]

      BMIz will be calculated based on the participant's age, height, and weight using the CDC 2000 growth charts. To identify where physical activity occurs, children will wear the QStarz BT Q1000XT data logger for 7 days concurrent with the ActiGraph GT3X+. In regards to the environmental factors, parents of participants will complete the Neighborhood Impact on Kids (NIK) survey, and participants will complete a neighborhood perceptions survey. In regards to socio-emotional factors, participants will complete the Body Image Assessment for Preadolescents, the Mood and Feelings Questionnaire, the Health-Related Quality of Life, the Personal Experiences Checklist related to stress, and the Food Craving Inventory. Further, participants will record negative and positive affect during a 7-day period by responding to prompts on a mobile phone-based app, using ecological momentary assessment.

    Secondary Outcome Measures

    1. Objective 1 Secondary Analysis: Change in daily moderate to vigorous physical activity (MVPA) minutes between years. [Year 0 and Year 2]

      MVPA measured by a triaxial accelerometer (Actigraph GT3X+, Actigraph of Ft. Walton Beach, FL) as described in outcome 1. Participants will also complete a Lifestyle survey to collect information including physical activity habits.

    2. Objective 1 Secondary Analysis: Change in days/week of physical activity between years. [Year 0 and Year 2]

      MVPA measured by a triaxial accelerometer (Actigraph GT3X+, Actigraph of Ft. Walton Beach, FL) as described in outcome 1. Participants will also complete a Lifestyle survey to collect information including physical activity habits.

    3. Objective 2 Secondary Analysis: Relationship between fat mass accumulation and change in physical activity. [Year 0 and Year 2]

      Body composition will be determined by DXA and MRI. With DXA, total body fat and trunk fat will be measured by whole-body DXA using a GE iDXA scanner (GE Medical Systems, Milwaukee, WI) to quantify total and regional body fat (including trunk fat). MRI - Visceral fat, i.e. visceral adipose tissue, will be measured by water-fat shifting MRI using the General Electric Discovery 750w 3.0 Tesla (GE Medical Systems, Milwaukee, WI). IDEAL-IQ imaging technique will be used to generate water-only, fat-only, in-phase, and out-of-phase echoes in a single acquisition with a 20-second breath-hold. Physical Activity will be measured by a triaxial accelerometer as described in outcome 1. Participants will also complete a Lifestyle survey to collect information including physical activity habits.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    10 Years to 16 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Age 10-16 years

    • Body weight < 500 lbs.

    • Ability to understand instructions and complete all study procedures

    Exclusion Criteria:
    • Pregnant

    • On a restrictive diet due to illness

    • Significant physical or mental disabilities that impede walking, wearing accelerometer or GPS, or responding to EMA.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Pennington Biomedical Research Center Baton Rouge Louisiana United States 70808

    Sponsors and Collaborators

    • Pennington Biomedical Research Center
    • USDA Beltsville Human Nutrition Research Center

    Investigators

    • Principal Investigator: Amanda E Staiano, PhD, PBRC Assistant Professor

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Amanda Staiano, PBRC Assistant Professor, Pennington Biomedical Research Center
    ClinicalTrials.gov Identifier:
    NCT02784509
    Other Study ID Numbers:
    • PBRC 2016-028
    • 3092-51000-04A
    First Posted:
    May 27, 2016
    Last Update Posted:
    Jan 18, 2022
    Last Verified:
    Jan 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by Amanda Staiano, PBRC Assistant Professor, Pennington Biomedical Research Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 18, 2022