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Clinical Trials/NCT01109797
NCT01109797CompletedNot Applicable

A Comparison of Two Models for Transition of Adolescents and Young Adults With Diabetes From Pediatric to Adult Care

University of Kansas1 site in 1 country28 target enrollmentStarted: April 1, 2010Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
28
Locations
1
Primary Endpoint
Measure and compare change in self-efficacy and change in diabetes knowledge, diabetes quality of life, family conflict, and treatment satisfaction for and between the two groups.

Study Overview

Brief Summary

The purpose of the study is to compare two interventions for preparing diabetic teens and young adults for transition from pediatric to adult diabetes care.

Detailed Description

One will represent a short-term intensive social-behavioral intervention supported by peer-to-peer social networking in which subjects receive "usual care" from their current diabetes provider outside the parameters of the study. The second intervention will be a traditional transition clinic model, where subjects will receive the standard of diabetes care from a team of combined pediatric and adult practitioners and educators, with added educational modules and behavioral evaluation and support designed to facilitate the transition to adult care (i.e., that foster "developmentally tailored care"). The first is a much less intensive intervention from the standpoint of the providers and gives special prominence to peer support; the second is provider-intensive. The goal of both interventions is to improve self-efficacy (confidence in taking ownership of and managing one's diabetes); i.e., to prepare the patient to move from primary support by family and providers to a reliance on self-ownership and self-management as a responsible, independent adult.

Optional sub-study available for parents, spouses, and significant others.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
16 Years to 29 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age 16-29
  • •Diagnosis of type 1 diabetes, or type 2 diabetes managed with insulin, at least one year prior to study initiation
  • •English-speaking
  • •Some form of private or public (e.g., Medicaid) health insurance

Exclusion Criteria

  • •Cystic fibrosis-related or pancreatitis-related diabetes
  • •Diabetes related to a known specific genetic defect such as Down's Syndrome, Lipoatrophic Diabetes, Leprechaunism or Rabson-Mendenhall Syndrome, etc.
  • •Chronic liver disease
  • •History of chronic renal failure
  • •Serious psychiatric illness that in the judgment of the investigators would preclude the individual's ability to complete the study
  • •Pregnant or planning to become pregnant within 6 months

Arms & Interventions

Transition Social Behavioral Intervention

Experimental

Intervention: Transition Social Behavioral Intervention (Behavioral)

Diabetes Transition Clinic

Experimental

Intervention: Diabetes Transition Clinic (Behavioral)

Outcomes

Primary Outcomes

Measure and compare change in self-efficacy and change in diabetes knowledge, diabetes quality of life, family conflict, and treatment satisfaction for and between the two groups.

Time Frame: 6 months and 12 months

Secondary Outcomes

  • Make exploratory baseline comparisons between the two groups regarding locus of diabetes care (kind of provider), comparing numbers of subjects in each group who made a successful transition to adult care(6 months and 12 months)
  • Make exploratory baseline comparisons between the two groups of using some form of social networking by the two groups as an adjunt of diabetes care.(6 months and 12 months)
  • Make exploratory baseline comparisons between the two groups regarding provider and educator time devoted in each arm of the intervention (in order to prepare for a robust comparative effectiveness analysis in a subsequent study).(6 months)
  • Make exploratory baseline comparisons between the two groups of HgbA1c(6 months and 12 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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