Study to Test Use of a Decision Aid in a Clinical Visit to Help Patients Choose a Diabetes Medication (TRICEP)
Primary Purpose
Type 2 Diabetes Mellitus
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Diabetes Medication Choice Cards
Sponsored by

About this trial
This is an interventional supportive care trial for Type 2 Diabetes Mellitus focused on measuring Decision Aids, Shared Medical Decision Making, Patient Education, Endocrine System Diseases, Glucose Metabolism Disorders, Metabolic Diseases
Eligibility Criteria
Inclusion Criteria:
- 18 years of age and older
- Have a diagnosis of Type 2 diabetes mellitus and on diabetes medication
- Have a diagnosis of Type 2 diabetes mellitus for 1 year or more if not currently on diabetes medication
- Recognize their primary care provider as their main diabetes care provider
- Use 0, 1, 2, or 3 oral hypoglycemic agents
- Have a recent HbA1c measure (within 12 months) of greater than 7.3, with priority to patients with rising HbA1c levels.
Exclusion Criteria:
- Not available for follow-up for 12 months after study visit.
- Unable to read and speak English.
- Has major barriers to providing written informed consent.
Sites / Locations
- Albert Lea Medical Center
- Mayo Clinic Kasson
- Mayo Clinic Health System- Immanual St. Joseph's
- Hennepin County Medical Center
- Park Nicollet Institute
- Mayo Clinic Health System-Franciscan Healthcare
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Usual Care
Diabetes Medication Decision Aid
Arm Description
Clinicians will present diabetes medication options to patients, in their usual way.
In the decision aid arm, clinicians will use the diabetes medication decision aid cards (if they choose) when discussing diabetes medication options with their patients.
Outcomes
Primary Outcome Measures
Patient Satisfaction and knowledge
Primary outcome is to evaluate the impact of our decision aid (Diabetes Medication Choice Cards) versus usual care as strategies to translate CER into practice among patients with poorly controlled diabetes in need of drug intensification (Hemoglobin A1c (HbA1c) > 7.3%). Patient outcomes include satisfaction with use of the decision aid and knowledge, compared to the control, usual care group (by written survey at point of care and follow-up).
Secondary Outcome Measures
Physician adoption and satisfaction with the decision aid.
Brief post-visit surveys will be completed by the clinicians, directly following clinical visit.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01293578
Brief Title
Study to Test Use of a Decision Aid in a Clinical Visit to Help Patients Choose a Diabetes Medication
Acronym
TRICEP
Official Title
Translating Information on Comparative Effectiveness Into Practice (TRICEP)
Study Type
Interventional
2. Study Status
Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
June 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The goal of this study is to test the relative merits of a decision aid for diabetes medications that we have developed - Diabetes Medication Choice Cards- versus usual care in translating comparative effectiveness research (CER) into real world clinics. This study will involve about 20 primary care practice sites affiliated with Mayo Health System, Park Nicollet, or Hennepin County Medical Center. There will be no recruiting done at the Mayo Clinic.
Detailed Description
To conduct a cluster-randomized practical trial to evaluate the impact of our decision aid (Diabetes Medication Choice Cards) versus usual care as strategies to translate CER into practice among patients with poorly controlled diabetes in need of drug intensification (Hemoglobin Alc (HbA1c) > 7.3%). Patient outcomes including reaching glycemic control target (HbA1c less than or equal to 7.3%), medication choice and adherence, satisfaction and knowledge. From the physician perspective, we will be measuring physician adoption and satisfaction with the decision aid.
To identify, describe, and explain factors that promote or inhibit the uptake of complex interventions such as decision aids in practices participating in the trial.
To conduct an exploratory analysis of the ability of patients to adhere to the medications chosen while exploring the factors that enable or hinder the patients' ability to incorporate these medications into their routine.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes Mellitus
Keywords
Decision Aids, Shared Medical Decision Making, Patient Education, Endocrine System Diseases, Glucose Metabolism Disorders, Metabolic Diseases
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
550 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
Clinicians will present diabetes medication options to patients, in their usual way.
Arm Title
Diabetes Medication Decision Aid
Arm Type
Experimental
Arm Description
In the decision aid arm, clinicians will use the diabetes medication decision aid cards (if they choose) when discussing diabetes medication options with their patients.
Intervention Type
Other
Intervention Name(s)
Diabetes Medication Choice Cards
Intervention Description
Clinician uses the Diabetes Medication Choice Cards to inform and engage patient in discussing the issues they find relevant in choosing a new diabetes medication.
Primary Outcome Measure Information:
Title
Patient Satisfaction and knowledge
Description
Primary outcome is to evaluate the impact of our decision aid (Diabetes Medication Choice Cards) versus usual care as strategies to translate CER into practice among patients with poorly controlled diabetes in need of drug intensification (Hemoglobin A1c (HbA1c) > 7.3%). Patient outcomes include satisfaction with use of the decision aid and knowledge, compared to the control, usual care group (by written survey at point of care and follow-up).
Time Frame
baseline to 12 months
Secondary Outcome Measure Information:
Title
Physician adoption and satisfaction with the decision aid.
Description
Brief post-visit surveys will be completed by the clinicians, directly following clinical visit.
Time Frame
baseline to 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
18 years of age and older
Have a diagnosis of Type 2 diabetes mellitus and on diabetes medication
Have a diagnosis of Type 2 diabetes mellitus for 1 year or more if not currently on diabetes medication
Recognize their primary care provider as their main diabetes care provider
Use 0, 1, 2, or 3 oral hypoglycemic agents
Have a recent HbA1c measure (within 12 months) of greater than 7.3, with priority to patients with rising HbA1c levels.
Exclusion Criteria:
Not available for follow-up for 12 months after study visit.
Unable to read and speak English.
Has major barriers to providing written informed consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Victor Montori, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Albert Lea Medical Center
City
Albert Lea
State/Province
Minnesota
ZIP/Postal Code
56007
Country
United States
Facility Name
Mayo Clinic Kasson
City
Kasson
State/Province
Minnesota
ZIP/Postal Code
55944
Country
United States
Facility Name
Mayo Clinic Health System- Immanual St. Joseph's
City
Mankato
State/Province
Minnesota
ZIP/Postal Code
56002
Country
United States
Facility Name
Hennepin County Medical Center
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55415
Country
United States
Facility Name
Park Nicollet Institute
City
Saint Louis Park
State/Province
Minnesota
ZIP/Postal Code
55416
Country
United States
Facility Name
Mayo Clinic Health System-Franciscan Healthcare
City
La Crosse
State/Province
Wisconsin
ZIP/Postal Code
54601
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
34499328
Citation
Kunneman M, Branda ME, Ridgeway JL, Tiedje K, May CR, Linzer M, Inselman J, Buffington ALH, Coffey J, Boehm D, Deming J, Dick S, van Houten H, LeBlanc A, Liesinger J, Lima J, Nordeen J, Pencille L, Poplau S, Reed S, Vannelli A, Yost KJ, Ziegenfuss JY, Smith SA, Montori VM, Shah ND. Making sense of diabetes medication decisions: a mixed methods cluster randomized trial using a conversation aid intervention. Endocrine. 2022 Feb;75(2):377-391. doi: 10.1007/s12020-021-02861-4. Epub 2021 Sep 9. Erratum In: Endocrine. 2023 Jan;79(1):221-222.
Results Reference
result
Links:
URL
https://www.mayo.edu/research/clinical-trials
Description
Mayo Clinic Clinical Trials
Learn more about this trial
Study to Test Use of a Decision Aid in a Clinical Visit to Help Patients Choose a Diabetes Medication
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