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Shared Medical Decision Making in Pediatric Diabetes

Primary Purpose

Type 1 Diabetes Mellitus

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Usual Clinical Practice
Shared Medical Decision Making
Sponsored by
Nemours Children's Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Type 1 Diabetes Mellitus focused on measuring type 1 diabetes mellitus, adolescence, adherence, insulin pump, continuous subcutaneous insulin infusion, continuous glucose monitor, shared medical decision making

Eligibility Criteria

11 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Type 1 diabetes for 1 year or more
  • At least 2 diabetes clinic visits at the enrolling site in the prior year
  • Considered by treating endocrinologist to be a candidate for insulin pump or continuous glucose monitor
  • Intent to continue care at Nemours for 1 year
  • Internet access at home, school, work or relative's home

Exclusion Criteria:

  • Open case with child protection agency
  • Unable to read and speak English

Sites / Locations

  • Nemours Children's Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Usual Clinical Practice (UCP)

Shared Medical Decision Making (SMDM)

Arm Description

UCP participants will receive the same clinical and educational management for candidates for insulin pump or continuous glucose monitoring that is received by similar patients who are not enrolled in this study. The respective endocrinology practices at the enrolling sites all strive to meet or exceed the current American Diabetes Association Standards for Clinical Practice in the management of type 1 diabetes in this population. Thorough patient education is the cornerstone of that care, especially regarding the incorporation of insulin pumps and continuous glucose monitors into the treatment regimen for a given patient.

Participants randomized to SMDM receive all components of UCP supplemented with access to the decision aid website pertinent to the medical decision of interest (pump or CGM). Adolescents and parents will receive password-protected, secure access to the decision for their use until a decision is reached. The platform will then generate a summary report that the adolescent and parent will discuss with a diabetes nurse and then a visit with the treating endocrinologist will be scheduled to conclude the SMDM intervention for that adolescent and parent.

Outcomes

Primary Outcome Measures

Device utilization
Downloaded data from insulin pump or continuous glucose monitor

Secondary Outcome Measures

Glycated hemoglobin (Hemoglobin A1C)
Glycated hemoglobin (Hemoglobin A1C)
Hypoglycemia Diary
Frequency of severe and symptomatic hypoglycemic episodes
Decision quality
Questionnaires measuring decision making satisfaction and regret.
Knowledge of insulin pump or continuous glucose monitor
Brief test of parent and adolescent knowledge about the pertinent device and its use.
Diabetes Self Management Profile Self Report Form
Measure of diabetes treatment adherence completed by parents and adolescents.

Full Information

First Posted
April 23, 2015
Last Updated
February 8, 2017
Sponsor
Nemours Children's Clinic
Collaborators
Patient-Centered Outcomes Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT02496156
Brief Title
Shared Medical Decision Making in Pediatric Diabetes
Official Title
Shared Medical Decision Making in Pediatric Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
February 2015 (undefined)
Primary Completion Date
February 7, 2017 (Actual)
Study Completion Date
February 7, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nemours Children's Clinic
Collaborators
Patient-Centered Outcomes Research Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This work is testing a shared medical decision making intervention for adolescents with type 1 diabetes and their parents who are candidates for adding either an insulin pump or continuous glucose monitor to their treatment plan. The first half of the work consisted of the stakeholder driven design, construction and refinement of web-delivered multimedia decision aids for each of these decisions. The randomized controlled trial of that intervention began enroling participants in February 2015. A sample of 166 eligible adolescents who receive care at an operating entity of the Nemours Children's Health System will be enrolled and randomized to either Usual Clinical Practice alone or augmented by the Shared Medical Decision Making intervention. Primary outcomes include measures of engagement with the pertinent technology if it is chosen and measures of decision quality; Secondary outcomes include indices of metabolic control, quality of life and parent-adolescent relationships around diabetes management.
Detailed Description
Abstract (modified after achievement of Aims 1 and 2): Treatment adherence in type 1 diabetes (T1D) tends to decline among adolescents, increasing risks of acute and chronic complications, excess health care use, poorer quality of life, and T1D-related family conflict. Poor adherence is associated with psychiatric and family dysfunction and often persists into early adulthood. Therapeutic advances such as continuous subcutaneous insulin infusion (CSII or "insulin pump") and continuous glucose monitoring (CGM) could improve metabolic control and quality of life. But, teens often do not benefit fully from such advances. Many studies of adults show that patient-centered communication styles predict more favorable clinical outcomes. Shared medical decision making (SMDM) interventions have improved outcomes among adults with diabetes and other conditions. Research in pediatrics has also shown that patient-centered and family-centered communication styles predict favorable outcomes, but most of this research is in primary care and has not studied youth with chronic conditions. Since there have been no controlled trials of SMDM with chronically ill youths, we propose a randomized controlled trial of an SMDM intervention compared with Usual Clinical Practice (UCP). Qualitative interviews of youths and parents who have previously faced these decisions and reliance on expert consultants, pediatric endocrinologists and diabetes educators have preceded this trial and provided valued input for refining the planned intervention and adapting the structured SMDM format for pediatrics. Now, we will recruit and randomize 166 11-<17 year old youth with T1D who are candidates for CSII or CGM (and a parent/caregiver) at all Nemours sites. The SMDM intervention will be delivered via a web-based platform, facilitated by Diabetes Educators (DEs) at each site in a standardized, yet individually tailored format. SMDM will employ multimedia "decision aids" prepared with the award-winning Nemours Center for Children's Health Media and the "e-city interactive" web design firm in Philadelphia in accord with pertinent international standards. SMDM will also include individualized assistance from the DE in assuring that each youth's and parent's preferences, values and cultural beliefs are carefully addressed and communicated to the attending endocrinologist. After a baseline evaluation and randomization to SMDM or UCP, effects on the primary outcome (treatment adherence; device utilization) and secondary outcomes (glycemic control, treatment alliance, decision conflict and regret, treatment satisfaction, diabetes-related distress and self-efficacy) will be measured over 1 year. Mixed effects modeling will be the primary analytic technique for evaluating effects on primary/secondary outcomes, examining selected variables as moderators and mediators of treatment effects, and assessing whether such effects are comparable for the two medical decisions of interest. The results will verify whether SMDM in this context enhances treatment adherence, device use and parent/patient-reported outcomes in youth with T1D.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes Mellitus
Keywords
type 1 diabetes mellitus, adolescence, adherence, insulin pump, continuous subcutaneous insulin infusion, continuous glucose monitor, shared medical decision making

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
2 group (Usual Clinical Practice or Shared Medical Decision Making X 5 time points (0, 3, 6, 9 and 12 months) repeated measures randomized treatments design.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
153 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Usual Clinical Practice (UCP)
Arm Type
Active Comparator
Arm Description
UCP participants will receive the same clinical and educational management for candidates for insulin pump or continuous glucose monitoring that is received by similar patients who are not enrolled in this study. The respective endocrinology practices at the enrolling sites all strive to meet or exceed the current American Diabetes Association Standards for Clinical Practice in the management of type 1 diabetes in this population. Thorough patient education is the cornerstone of that care, especially regarding the incorporation of insulin pumps and continuous glucose monitors into the treatment regimen for a given patient.
Arm Title
Shared Medical Decision Making (SMDM)
Arm Type
Experimental
Arm Description
Participants randomized to SMDM receive all components of UCP supplemented with access to the decision aid website pertinent to the medical decision of interest (pump or CGM). Adolescents and parents will receive password-protected, secure access to the decision for their use until a decision is reached. The platform will then generate a summary report that the adolescent and parent will discuss with a diabetes nurse and then a visit with the treating endocrinologist will be scheduled to conclude the SMDM intervention for that adolescent and parent.
Intervention Type
Behavioral
Intervention Name(s)
Usual Clinical Practice
Intervention Description
Diabetes management and education related to insulin pump or continuous glucose monitor as currently practiced at the enrolling site.
Intervention Type
Behavioral
Intervention Name(s)
Shared Medical Decision Making
Intervention Description
Access to and use of multimedia decision aid websites to facilitate adolescent and parent decision making about incorporating these devices into the diabetes management regimen.
Primary Outcome Measure Information:
Title
Device utilization
Description
Downloaded data from insulin pump or continuous glucose monitor
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Glycated hemoglobin (Hemoglobin A1C)
Description
Glycated hemoglobin (Hemoglobin A1C)
Time Frame
Quarterly for 1 year
Title
Hypoglycemia Diary
Description
Frequency of severe and symptomatic hypoglycemic episodes
Time Frame
Continuous for one year
Title
Decision quality
Description
Questionnaires measuring decision making satisfaction and regret.
Time Frame
Quarterly for 1 year
Title
Knowledge of insulin pump or continuous glucose monitor
Description
Brief test of parent and adolescent knowledge about the pertinent device and its use.
Time Frame
Baseline and 3 months later
Title
Diabetes Self Management Profile Self Report Form
Description
Measure of diabetes treatment adherence completed by parents and adolescents.
Time Frame
Baseline and each 3 months throughout the study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
11 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Type 1 diabetes for 1 year or more At least 2 diabetes clinic visits at the enrolling site in the prior year Considered by treating endocrinologist to be a candidate for insulin pump or continuous glucose monitor Intent to continue care at Nemours for 1 year Internet access at home, school, work or relative's home Exclusion Criteria: Open case with child protection agency Unable to read and speak English
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tim Wysocki, PhD
Organizational Affiliation
Nemours Biomedical Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nemours Children's Clinic
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
27150606
Citation
Wysocki T, Hirschfeld F, Miller L, Izenberg N, Dowshen SA, Taylor A, Milkes A, Shinseki MT, Bejarano C, Kozikowski C, Kowal K, Starr-Ashton P, Ross JL, Kummer M, Carakushansky M, Lyness D, Brinkman W, Pierce J, Fiks A, Christofferson J, Rafalko J, Lawson ML. Consideration of Insulin Pumps or Continuous Glucose Monitors by Adolescents With Type 1 Diabetes and Their Parents: Stakeholder Engagement in the Design of Web-Based Decision Aids. Diabetes Educ. 2016 Aug;42(4):395-407. doi: 10.1177/0145721716647492. Epub 2016 May 4.
Results Reference
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Shared Medical Decision Making in Pediatric Diabetes

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