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Family Focused Community Program to Prevent Type 2 Diabetes in Peripubertal Youth (EPIC Kids)

Primary Purpose

Pediatric Obesity

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
YMCA Family Diabetes Prevention Program (YFDPP)
Sponsored by
University of Arizona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pediatric Obesity focused on measuring Intervention Studies

Eligibility Criteria

9 Years - 12 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Inclusion Criteria for Children and Parents/Primary Caregivers

  • child's age between 9 to 12 years
  • child body mass index (BMI) 85th percentile for age and sex
  • child has T2D risk factors:

    • 1st or 2nd degree relative with T2D
    • conditions associated with insulin resistance/metabolic syndrome (e,g, acanthosis nigricans, hypertension, dyslipidemia, PCOS, or small for gestational age birth weight, maternal history of T2D or gestational diabetes)
  • parent/primary caregiver must be willing to participate in intervention sessions and activities (note: primary caregiver is the adult guardian who most frequently prepares/obtains food, regulates media use, and provides physical activity opportunities for the child)
  • parent/child willing to use a study-provided mobile device during intervention
  • parent and child speak and read English

Exclusion Criteria:

Exclusion Criteria for Children (Index Participants) and Parents/Primary Caregivers

  • child/parent unwillingness to participate in group activities or to use study-provided mobile device
  • child previously diagnosed T1 or T2D
  • child with psychiatric disturbances or mental illness
  • child with inability to be physically active
  • child/parent inability to speak and read English
  • child takes weight loss medications or medications known to cause weight gain or affect appetite.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    face-to-face

    face-to-face + mobile hybrid

    Arm Description

    Delivery and testing of YMCA Family Diabetes Prevention Program (YFDPP) delivered face-to-face by YMCAs over 12 weeks to children age 9-12 and one parent/guardian.

    Delivery and testing of YMCA Family Diabetes Prevention Program (YFDPP) delivered face-to-face and via a mobile platform by YMCAs over 12 weeks to children age 9-12 and one parent/guardian.

    Outcomes

    Primary Outcome Measures

    Change in percentage overweight
    Percentage overweight will be calculated as percentage over the median body mass index (BMI) for age and gender

    Secondary Outcome Measures

    Blood pressure
    Systolic and diastolic blood pressure
    Fasting insulin
    Fasting glucose
    Fasting lipids
    Total cholesterol, Triglycerides, HDL, and LDL
    Dietary intake
    2, 24-hour dietary recalls
    Physical activity
    accelerometry
    Waist circumference
    Waist circumference at umbilicus

    Full Information

    First Posted
    April 15, 2015
    Last Updated
    October 24, 2016
    Sponsor
    University of Arizona
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02421198
    Brief Title
    Family Focused Community Program to Prevent Type 2 Diabetes in Peripubertal Youth
    Acronym
    EPIC Kids
    Official Title
    Family Focused Community Program to Prevent Type 2 Diabetes in Peripubertal Youth
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2016
    Overall Recruitment Status
    Completed
    Study Start Date
    May 2015 (undefined)
    Primary Completion Date
    July 2016 (Actual)
    Study Completion Date
    July 2016 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Arizona

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Over one-third of children and adolescents are overweight and nearly 1 in 5 of them are obese. Metabolic syndrome, a strong predictor of Type 2 diabetes (T2D) and cardiovascular disease (CVD), occurs in up to 44% of obese youth, foreshadowing greater prevalence and earlier onset of T2D. Without effective interventions, "diabesity" will worsen, T2D prevalence will increase, and adults will face its consequences at younger ages. Given the strong association between obesity and chronic disease risk factors in youth, the investigators contend T2D prevention (and CVD prevention) is akin to weight control and obesity prevention. The objective of the proposed project is to develop a family-centered, community-based program for T2D prevention in peripubertal (9- to 12-year-old) youth. Using participatory methods, the investigators intend to adapt the successful adult-focused YMCA Diabetes Prevention Program (YDPP) for youth and families and assess the feasibility, participant acceptance of and adherence to the YFDPP using two delivery formats: a 12-week YMCA-based face-to-face program and a 12-week combined face-to-face plus mobile device-based program. The proposed study will test the investigators premise that delivery with technology can reduce participant perceived burden, improve adherence, and lead to improved anthropometric (height, weight and BMI and waist circumference), behavioral (diet and physical activity) and physiological outcomes (fasting insulin, glucose, lipid, blood pressure). The investigators will use the resulting data to design an appropriately powered full-scale trial. The importance of the proposed study is underscored both by the statistics cited above and the recent call for proposals to translate efficacious clinical interventions into effective community programs for youth. The potential impact of the proposed intervention is great in that the program will be delivered by paraprofessionals from the community without university researchers; significant in that it targets a major public health challenge in children and includes assessment of objective behavioral and clinical data; and innovative in that it focuses on an at-risk population, takes place at a popular, accessible community venue, and uses mobile technologies to extend reach and increase engagement of youth and families with intervention content. The long-term goal is to create a scalable, replicable, and sustainable program that overcomes existing barriers to implementation and dissemination of evidence-based, research-proven diabetes prevention programs to youth and families, thereby improving population health.
    Detailed Description
    The investigators objective is to develop a family-centered, community-based program for T2D prevention in peripubertal (9-12-year-old) youth. Efficacious community programs for youth are not available (although promising components exist), and thus the investigators propose to adapt the successful adult-focused YMCA Diabetes Prevention Program (YDPP) for youth and families, and assess its impact on anthropometric, behavioral and physiological outcomes in support of the design (power calculation) of a full-scale trial. The proposed study will evaluate the adapted program using two formats (with and without mobile technologies). Secondary endpoints will include participant perceived burden, adherence, and program costs. Aim 1: Adapt an efficacious diabetes prevention program in adults (the YMCA Diabetes Prevention Program, or YDPP) for delivery to overweight peripubertal youth and their families, thereby establishing a YMCA Family Diabetes Prevention Program (YFDPP). Aim 2: Test the feasibility, participant acceptance (child and parent) and retention rates of the YFDPP using two formats, a 12-week YMCA-based face-to-face program and a 12-week program with content delivered through a combination of face-to-face and mobile devices. Aim 3: Test the impact of the new YFDPP using two formats on anthropometric (height, weight, BMI and waist circumference), behavioral (diet and physical activity), and physiological (fasting insulin, glucose, lipid) outcomes, using the resulting data to design an appropriately powered full-scale trial.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Pediatric Obesity
    Keywords
    Intervention Studies

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    47 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    face-to-face
    Arm Type
    Experimental
    Arm Description
    Delivery and testing of YMCA Family Diabetes Prevention Program (YFDPP) delivered face-to-face by YMCAs over 12 weeks to children age 9-12 and one parent/guardian.
    Arm Title
    face-to-face + mobile hybrid
    Arm Type
    Experimental
    Arm Description
    Delivery and testing of YMCA Family Diabetes Prevention Program (YFDPP) delivered face-to-face and via a mobile platform by YMCAs over 12 weeks to children age 9-12 and one parent/guardian.
    Intervention Type
    Behavioral
    Intervention Name(s)
    YMCA Family Diabetes Prevention Program (YFDPP)
    Intervention Description
    12 week, group education to promote behavioral change delivered either face-to-face or via a combination of face-to-face and mobile technologies
    Primary Outcome Measure Information:
    Title
    Change in percentage overweight
    Description
    Percentage overweight will be calculated as percentage over the median body mass index (BMI) for age and gender
    Time Frame
    Baseline, Week 12 (post-intervention), Week 24
    Secondary Outcome Measure Information:
    Title
    Blood pressure
    Description
    Systolic and diastolic blood pressure
    Time Frame
    Baseline, Week 12 (post-intervention), Week 24
    Title
    Fasting insulin
    Time Frame
    Baseline, Week 12 (post-intervention), Week 24
    Title
    Fasting glucose
    Time Frame
    Baseline, Week 12 (post-intervention), Week 24
    Title
    Fasting lipids
    Description
    Total cholesterol, Triglycerides, HDL, and LDL
    Time Frame
    Baseline, Week 12 (post-intervention), Week 24
    Title
    Dietary intake
    Description
    2, 24-hour dietary recalls
    Time Frame
    Baseline, Week 12 (post-intervention), Week 24
    Title
    Physical activity
    Description
    accelerometry
    Time Frame
    Baseline, Week 12 (post-intervention), Week 24
    Title
    Waist circumference
    Description
    Waist circumference at umbilicus
    Time Frame
    Baseline, Week 12 (post-intervention), Week 24

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    9 Years
    Maximum Age & Unit of Time
    12 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Inclusion Criteria for Children and Parents/Primary Caregivers child's age between 9 to 12 years child body mass index (BMI) 85th percentile for age and sex child has T2D risk factors: 1st or 2nd degree relative with T2D conditions associated with insulin resistance/metabolic syndrome (e,g, acanthosis nigricans, hypertension, dyslipidemia, PCOS, or small for gestational age birth weight, maternal history of T2D or gestational diabetes) parent/primary caregiver must be willing to participate in intervention sessions and activities (note: primary caregiver is the adult guardian who most frequently prepares/obtains food, regulates media use, and provides physical activity opportunities for the child) parent/child willing to use a study-provided mobile device during intervention parent and child speak and read English Exclusion Criteria: Exclusion Criteria for Children (Index Participants) and Parents/Primary Caregivers child/parent unwillingness to participate in group activities or to use study-provided mobile device child previously diagnosed T1 or T2D child with psychiatric disturbances or mental illness child with inability to be physically active child/parent inability to speak and read English child takes weight loss medications or medications known to cause weight gain or affect appetite.

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    26679186
    Citation
    Hingle MD, Turner T, Kutob R, Merchant N, Roe DJ, Stump C, Going SB. The EPIC Kids Study: a randomized family-focused YMCA-based intervention to prevent type 2 diabetes in at-risk youth. BMC Public Health. 2015 Dec 18;15:1253. doi: 10.1186/s12889-015-2595-3.
    Results Reference
    derived

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