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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01293578
Other study ID # 10-006952
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2011
Est. completion date June 2015

Study information

Verified date September 2022
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 550
Est. completion date June 2015
Est. primary completion date June 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Diabetes Medication Choice Cards
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.

Locations

Country Name City State
United States Albert Lea Medical Center Albert Lea Minnesota
United States Mayo Clinic Kasson Kasson Minnesota
United States Mayo Clinic Health System-Franciscan Healthcare La Crosse Wisconsin
United States Mayo Clinic Health System- Immanual St. Joseph's Mankato Minnesota
United States Hennepin County Medical Center Minneapolis Minnesota
United States Park Nicollet Institute Saint Louis Park Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

References & Publications (1)

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, Smi — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary 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). baseline to 12 months
Secondary Physician adoption and satisfaction with the decision aid. Brief post-visit surveys will be completed by the clinicians, directly following clinical visit. baseline to 12 months
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