Family Focused Community Program to Prevent Type 2 Diabetes in Peripubertal Youth

Pediatric Obesity Clinical Trial

— EPIC Kids  

Official title:

Family Focused Community Program to Prevent Type 2 Diabetes in Peripubertal Youth

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02421198
• Other study ID #: 1R21DK100805-01
• Status: Completed
• Phase: N/A
• First received: April 15, 2015
• Last updated: October 24, 2016
• Start date: May 2015
• Est. completion date: July 2016

Study information

• Verified date: October 2016
• Source: University of Arizona
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 47
• Est. completion date: July 2016
• Est. primary completion date: July 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 9 Years to 12 Years

Eligibility

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.

Related Conditions & MeSH terms

• Pediatric Obesity

Intervention

Behavioral:
• YMCA Family Diabetes Prevention Program (YFDPP)
12 week, group education to promote behavioral change delivered either face-to-face or via a combination of face-to-face and mobile technologies

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
University of Arizona

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in percentage overweight	Percentage overweight will be calculated as percentage over the median body mass index (BMI) for age and gender	Baseline, Week 12 (post-intervention), Week 24
Secondary	Blood pressure	Systolic and diastolic blood pressure	Baseline, Week 12 (post-intervention), Week 24
Secondary	Fasting insulin		Baseline, Week 12 (post-intervention), Week 24
Secondary	Fasting glucose		Baseline, Week 12 (post-intervention), Week 24
Secondary	Fasting lipids	Total cholesterol, Triglycerides, HDL, and LDL	Baseline, Week 12 (post-intervention), Week 24
Secondary	Dietary intake	2, 24-hour dietary recalls	Baseline, Week 12 (post-intervention), Week 24
Secondary	Physical activity	accelerometry	Baseline, Week 12 (post-intervention), Week 24
Secondary	Waist circumference	Waist circumference at umbilicus	Baseline, Week 12 (post-intervention), Week 24