REMEDIES4D: REdesigning MEDication Intensification Effectiveness Study for Diabetes

Type 2 Diabetes Clinical Trial

— Remedies4D  

Official title:

Redesigning Medication Intensification Effectiveness Study for Diabetes

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01611168
• Other study ID #: PRO08040023
• Status: Completed
• Phase: N/A
• Start date: April 2012
• Est. completion date: December 2015

Study information

• Verified date: May 2017
• Source: University of Pittsburgh
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The proposed research study aims to determine whether applying the University of Pittsburgh Medical Center Nurse-Directed Diabetes Management Protocols (NDMPs) leads to improved clinical outcome and process measures as recommended by American Diabetes Association (ADA), quality of life, treatment satisfaction and medication adherence for adults with diabetes, and favorable providers' satisfaction as compared to usual diabetes care. Furthermore, the cost-effectiveness of performing the NDMPs compared to usual diabetes care in primary care settings will also be assessed.

Description:

This proposed study is a multi-practice, cluster-design, prospective randomized controlled trial with a total study intervention period of 12 months. This prospective randomized controlled trial will assess the effectiveness of performing NDMPs by the registered nurse supervised by a physician (the intervention group) in comparison with usual diabetes care (the usual care group) for adults with diabetes in primary care settings. The study population will be recruited from University of Pittsburgh Medical Center Community Medicine Inc. (CMI) primary care practices in urban and suburban communities surrounding Pittsburgh, PA. Among these CMI practices, ten practices receive diabetes education services from University of Pittsburgh Diabetes Institute and will be the intervention group. These diabetes education services will be enhanced by the addition of NDMPs intervention. In addition, we will select another 10 CMI practices to be the usual care group. This group receives standard diabetes education with no use of NDMPs. One-hundred and fifty participants will be recruited across practices within each study group (i.e., 300 in total). Outcomes assessed in this study include clinical outcome and process measures as recommended by ADA, participants' quality of life, treatment satisfaction, and medication adherence, and providers' satisfaction, and costs/expenditure. Assessments will be done at baseline, and three and 12 months after the study entry. Analysis of the study outcomes will be based on intention-to-treat to determine (1) within-group differences between the baseline and follow-up visits, and (2) between-group differences between the intervention group and the usual care group.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 240
• Est. completion date: December 2015
• Est. primary completion date: December 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Adults aged 18 or greater

2. The diagnosis of type 2 diabetes of the subjects should be 1 year or more prior to the inception of this study

3. Subjects will be on medication treatment for their type 2 diabetes

4. Subjects' A1C levels should be higher than 7% for study entry

5. LDLc>100mg/d*l or

6. Blood Pressure >130/80*mg/dl

7. Any combination of the #4, 5 &6 At least one visit to the practice within the previous 12 months.

Exclusion Criteria:

1. Non-ambulatory

2. Gestational diabetes

3. Pregnant women (by self-report)

4. Subjects have received diabetes education services performed by the registered nurse from UPDI

5. Subjects are treated with exercise and diet only

6. Subjects are participating or will participate in other research studies

7. Subjects do not have insurance or cannot afford payments for diabetes care/treatment

8. Subjects are unable to read and comprehend English

9. Subjects are unable to provide informed consent

10. Other medical conditions for which these protocols are deemed inappropriate by the physician.

Related Conditions & MeSH terms

• Diabetes Mellitus
• Type 2 Diabetes

Intervention

Other:
• Treatment Algorithms
subjects in the intervention group will receive diabetes care from a well-trained registered nurse (RN) who will follow approved treatment algorithms/protocols for glycemia, high blood pressure, lipids and microalbuminuria.

Locations

Country	Name	City	State
United States	University of Pittsburgh Medical Center Community Medicine Inc. (UPMC CMI) Primary Care Practices	Pittsburgh	Pennsylvania

Sponsors (2)

Lead Sponsor	Collaborator
University of Pittsburgh	American Diabetes Association

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Glycated hemoglobin (A1C)	Change in HbA1c blood test	1 year
Primary	Blood pressure (systolic and diastolic blood pressure	Change in systolic and diastolic blood pressure reading	1 year
Primary	Lipids (LDLc, HDLc, cholesterol, and triglyceride)	Change in LDLc, HDLc, cholesterol, and triglyceride values	1 year