Journey for Control of Diabetes Study (0431-111)
Primary Purpose
Type 2 Diabetes Mellitus
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Interactive Dialogue to Educate and Activate (IDEA)
Individual Education (IE)
Sponsored by

About this trial
This is an interventional other trial for Type 2 Diabetes Mellitus
Eligibility Criteria
Inclusion Criteria:
- Type 2 Diabetes Mellitus
Exclusion Criteria:
- Gestational diabetes
- Type 1 Diabetes Mellitus
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
No Intervention
Arm Label
1
2
3
Arm Description
IDEA
IE
UC: Patients receive no research intervention.
Outcomes
Primary Outcome Measures
Program satisfaction, behavioral and emotional outcomes.
Secondary Outcome Measures
Blood sugar level, blood pressure, lipids, cost, comorbidities.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00652509
Brief Title
Journey for Control of Diabetes Study (0431-111)
Official Title
Journey for Control of Diabetes Study
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
May 1, 2008 (Actual)
Primary Completion Date
March 1, 2010 (Actual)
Study Completion Date
July 1, 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Merck Sharp & Dohme LLC
4. Oversight
5. Study Description
Brief Summary
Behavior change and self-efficacy are key for patients with diabetes to sustain blood sugar goals, but most care systems do not provide effective support to assist patients in successful ongoing self-management. After initial education, many programs are limited by allowable Medicare reimbursement for diabetes education which currently requires physician referral and cannot exceed two hours of training per year for a beneficiary, plus one hour of nutritional services. These services are usually provided either on an individual basis or occasionally through a traditional group class approach. For patients with established type 2 diabetes who are not achieving optimal glycemic control, we propose to develop and formally evaluate in a randomized trial a novel group experience to educate and motivate patients with established type 2 called IDEA, (Interactive Dialogue to Educate and Activate). This multi-site, randomized, prospective trial will randomize 621 patients with inadequately blood sugar control levels to one of 3 study groups: (1) IDEA - patients receive group sessions totaling 8 hours, with an average of 10 patients per group, using conversation maps as a conduit to facilitate dialogue between providers and patients (2) Individual Education (IE) - patients receive 2 hours with a nurse educator and 1 hour with a dietitian, and (3) Usual care (UC)- patients receive no research intervention. The primary analyses will involve mixed model regression to assess whether IDEA improves outcomes compared to IE and UC. Blood sugar level, blood pressure, and lipids will be evaluated 6 and12 months post-randomization and behavioral, emotional, and satisfaction outcomes through survey at baseline, 3, 6, 9 and 12 months. Depending on 12 month results, a longitudinal four year post intervention analysis is planned to assess sustainability of treatment effects and cost-effectiveness.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes Mellitus
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
621 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
IDEA
Arm Title
2
Arm Type
Active Comparator
Arm Description
IE
Arm Title
3
Arm Type
No Intervention
Arm Description
UC: Patients receive no research intervention.
Intervention Type
Behavioral
Intervention Name(s)
Interactive Dialogue to Educate and Activate (IDEA)
Intervention Description
IDEA - patients receive group sessions totaling 8 hours, with an average of 10 patients per group, using conversation maps as a conduit to facilitate dialogue between providers and patients.
Intervention Type
Behavioral
Intervention Name(s)
Individual Education (IE)
Intervention Description
IE - patients receive 2 hours with a nurse educator and 1 hour with a dietitian.
Primary Outcome Measure Information:
Title
Program satisfaction, behavioral and emotional outcomes.
Time Frame
3, 6, 9, 12 months after implementation of intervention
Secondary Outcome Measure Information:
Title
Blood sugar level, blood pressure, lipids, cost, comorbidities.
Time Frame
6, 12, 18, 24, 36, and 48 months after intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Type 2 Diabetes Mellitus
Exclusion Criteria:
Gestational diabetes
Type 1 Diabetes Mellitus
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Medical Director
Organizational Affiliation
Merck Sharp & Dohme LLC
Official's Role
Study Director
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
http://www.merck.com/clinical-trials/pdf/Merck%20Procedure%20on%20Clinical%20Trial%20Data%20Access%20Final_Updated%20July_9_2014.pdf
http://engagezone.msd.com/ds_documentation.php
Citations:
PubMed Identifier
21986350
Citation
Sperl-Hillen J, Beaton S, Fernandes O, Von Worley A, Vazquez-Benitez G, Parker E, Hanson A, Lavin-Tompkins J, Glasrud P, Davis H, Adams K, Parsons W, Spain CV. Comparative effectiveness of patient education methods for type 2 diabetes: a randomized controlled trial. Arch Intern Med. 2011 Dec 12;171(22):2001-10. doi: 10.1001/archinternmed.2011.507. Epub 2011 Oct 10.
Results Reference
derived
Learn more about this trial
Journey for Control of Diabetes Study (0431-111)
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