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Clinical Trials/NCT02700503
NCT02700503CompletedNot Applicable

Finding the Patient's Voice: Development of Practical Approaches for Adolescent and Family Focused Diabetes Prevention Programs

Indiana University3 sites in 1 country146 target enrollmentStarted: November 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
146
Locations
3
Primary Endpoint
Subject's BMI calculation Charted on CDC Stature for Age and Weight for Age Percentiles chart

Study Overview

Brief Summary

This study uses patient engagement to develop a diabetes prevention program focused on adolescents and families.

Detailed Description

Due to increases in obesity, the onset of type 2 diabetes is occurring at an ever-younger age, and is associated with poor outcomes and rising costs, which emphasizes the need for prevention at earlier ages. To address this need, the investigators designed the ENCOURAGE Healthy Families curriculum; a program based on the scientifically proven U.S. Diabetes Prevention Program, and while data demonstrate a reduction in obesity and diabetes risk for mothers and their children, the investigators have encountered several barriers to widespread implementation, including:

  1. helping youth/families understand the importance of prevention,
  2. on-going interest and participation, and
  3. differing personal beliefs.

Patient-centered research is needed to better understand what adolescents/families want in prevention initiatives, who should deliver program content, where and when to deliver programs in the community, and how adolescents/families wish to be informed of results. The investigators believe that by engaging patients and the community in the development process, the investigators will be able to obtain workable answers to these questions at a population level for high-risk youth/families in "real world" settings.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
10 Years to 18 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Overweight (BMI >85th percentile for age and sex, weight for height >85th percentile, or weight >120% of ideal [50th percentile] for height)
  • •At least two of the following risk factors:
  • •Have been diagnosed with prediabetes;
  • •Have a family history of T2DM in first- and second-degree relatives;
  • •Belong to a minority race/ethnic group (Native Americans, African-Americans, Hispanic Americans, Asians/South Pacific Islanders);
  • •Have conditions associated with insulin resistance; and/or
  • •Have had gestational diabetes or were exposed to gestational diabetes in utero.
  • •A family support person who is also willing to participate in the study. This person would preferably be a parent also at risk for diabetes (history of gestational diabetes, prediabetes, or with T2D).

Exclusion Criteria

  • •Type 2 diagnosis

Arms & Interventions

Intervention

Experimental

Participants will be enrolled in the ENCOURAGE 2.0 family-based diabetes prevention intervention that was designed through our work in Aims 1 and 2 of the study. It is this modified population-level ENCOURAGE 2.0 family-based diabetes prevention intervention that will be studied.

Intervention: Encourage 2.0 (Behavioral)

Outcomes

Primary Outcomes

Subject's BMI calculation Charted on CDC Stature for Age and Weight for Age Percentiles chart

Time Frame: 12 months

Secondary Outcomes

  • Intervention group session attendance(12 months)
  • Dietary records(12 months)
  • Physical activity(12 months)
  • Quality of life(12 months)
  • Hemoglobin A1C(12 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Tamara S. Hannon

Associate Professor of Pediatrics

Indiana University

Study Sites (3)

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