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ENhancing Outcomes Through Goal Assessment and Generating Engagement in Diabetes Mellitus (ENGAGE-DM)

Primary Purpose

Diabetes Mellitus Type 2

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Shared Decision Making
Sponsored by
AstraZeneca
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Diabetes Mellitus Type 2 focused on measuring Diabetes Mellitus Type 2

Eligibility Criteria

18 Years - 130 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion:

  • Commercially-insured beneficiaries
  • Receive all medical/prescription drug benefits through Horizon
  • On ≥1 one oral hypoglycemic agent
  • Latest HbA1c measurement ≥ 8% (within previous 6 months)
  • Provided phone number to Horizon

Exclusion:

- Currently using any insulin

Sites / Locations

  • Research Site

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

No Intervention

Arm Label

Shared Decision Making/Brief Negotiated Interviewing

Control Arm

Arm Description

This prospective study will include 700 beneficiaries of Horizon Blue Cross Blue Shield of New Jersey (BCBSNJ).

Seven hundred patients will also be identified by Horizon Analytics as a control group for analyses purposes only; these patients will not be contacted.

Outcomes

Primary Outcome Measures

Glycosylated Hemoglobin (HbA1c):
Pre- to post-intervention change in mean HbA1c levels

Secondary Outcome Measures

Medication Adherence (PDC Measure)
Mean Adherence (PDC) in each study arm in the follow-up period
Percentage (Proportion x 100) of Patients Achieving Optimal Adherence
Percentage (Proportion x 100) of patients in each study arm achieving optimal adherence (PDC ≥0.80) in the follow-up period
Patients Achieving HbA1c
Percentage (Proportion x 100) of patients in each study arm achieving optimal HbA1c control in the follow-up period

Full Information

First Posted
August 4, 2016
Last Updated
September 9, 2019
Sponsor
AstraZeneca
Collaborators
Brigham Women's Health
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1. Study Identification

Unique Protocol Identification Number
NCT02910089
Brief Title
ENhancing Outcomes Through Goal Assessment and Generating Engagement in Diabetes Mellitus
Acronym
ENGAGE-DM
Official Title
ENhancing Outcomes Through Goal Assessment and Generating Engagement in Diabetes Mellitus (ENGAGE-DM): A 12-month Study of the Impact of Combined Shared-decision Making and Brief Negotiated Interviewing on Disease Control and Medication Adherence in Patients With Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
October 20, 2016 (Actual)
Primary Completion Date
December 20, 2017 (Actual)
Study Completion Date
December 20, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AstraZeneca
Collaborators
Brigham Women's Health

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate whether a combination of pharmacist-delivered patient engagement techniques improves disease control and medication adherence among patients with poorly-controlled diabetes compared with usual care. These engagement techniques include shared decision-making and brief negotiated interviewing and are delivered telephonically.
Detailed Description
The US is facing a growing epidemic of type 2 diabetes. Among patients with poorly controlled diabetes, it is often not clear whether the problem is attributable to failure to appropriately intensify therapy, poor adherence to prescribed medications, unwillingness to accept new treatments or a combination of these factors. Multi-component pharmacist-delivered interventions, particularly those rooted in patient engagement, have been shown to be some of the most effective at improving adherence to chronic disease medications. Even though shared decision making and brief negotiated interviewing are complementary patient engagement techniques, the effectiveness of combining these 2 intervention approaches, especially in the management of diabetes, is unknown. In this study of patients using at least one oral hypoglycemic therapy with poorly controlled disease, the investigators examine the impact of a shared decision making and behavioral interviewing intervention delivered telephonically by pharmacists, compared with usual care. Briefly, all patients allocated to the intervention will be mailed a patient decision aid to prime them for encounters with pharmacists. After receiving the decision aid, these patients will be asked to engage in and provide informed consent for at least 4 telephonic discussions with pharmacists about their diabetes treatment options, goals, and preferences, medication adherence, strategies for reducing adherence barriers, and the benefits of maintaining blood glucose control. The study is being conducted within a large insurer and consists of 700 patients each allocated to the intervention group and the control group. Analyses will be performed on an intent-to-treat basis. After study completion, the investigators will also use predictive analytics to examine whether treatment response could be predicted based on patient characteristics, such as sociodemographic, clinical, medication use, and other motivational characteristics, which will provide information about which patients are most likely to benefit from the intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus Type 2
Keywords
Diabetes Mellitus Type 2

7. Study Design

Primary Purpose
Other
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1400 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Shared Decision Making/Brief Negotiated Interviewing
Arm Type
Other
Arm Description
This prospective study will include 700 beneficiaries of Horizon Blue Cross Blue Shield of New Jersey (BCBSNJ).
Arm Title
Control Arm
Arm Type
No Intervention
Arm Description
Seven hundred patients will also be identified by Horizon Analytics as a control group for analyses purposes only; these patients will not be contacted.
Intervention Type
Behavioral
Intervention Name(s)
Shared Decision Making
Intervention Description
This prospective study will include 700 beneficiaries of Horizon Blue Cross Blue Shield of New Jersey (BCBSNJ).
Primary Outcome Measure Information:
Title
Glycosylated Hemoglobin (HbA1c):
Description
Pre- to post-intervention change in mean HbA1c levels
Time Frame
baseline and at the end of 12 months post index date
Secondary Outcome Measure Information:
Title
Medication Adherence (PDC Measure)
Description
Mean Adherence (PDC) in each study arm in the follow-up period
Time Frame
during follow-up period of 12 months post index date
Title
Percentage (Proportion x 100) of Patients Achieving Optimal Adherence
Description
Percentage (Proportion x 100) of patients in each study arm achieving optimal adherence (PDC ≥0.80) in the follow-up period
Time Frame
during follow-up period of 12 months post index date
Title
Patients Achieving HbA1c
Description
Percentage (Proportion x 100) of patients in each study arm achieving optimal HbA1c control in the follow-up period
Time Frame
baseline and at the end of 12 months post index date

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
130 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion: Commercially-insured beneficiaries Receive all medical/prescription drug benefits through Horizon On ≥1 one oral hypoglycemic agent Latest HbA1c measurement ≥ 8% (within previous 6 months) Provided phone number to Horizon Exclusion: - Currently using any insulin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Niteesh K. Choudhry, MD, Ph.D
Organizational Affiliation
Brigham Women's Health
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Eric Wittbrodt, PharmD, MPH
Organizational Affiliation
AstraZeneca
Official's Role
Study Director
Facility Information:
Facility Name
Research Site
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
2115
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
30939143
Citation
Lauffenburger JC, Ghazinouri R, Jan S, Makanji S, Ferro CA, Lewey J, Wittbrodt E, Lee J, Haff N, Fontanet CP, Choudhry NK. Impact of a novel pharmacist-delivered behavioral intervention for patients with poorly-controlled diabetes: The ENhancing outcomes through Goal Assessment and Generating Engagement in Diabetes Mellitus (ENGAGE-DM) pragmatic randomized trial. PLoS One. 2019 Apr 2;14(4):e0214754. doi: 10.1371/journal.pone.0214754. eCollection 2019.
Results Reference
derived
Links:
URL
http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7111&studyid=4399&filename=D1843R00254_ENGAGE_SAP_RedactedPDFA.pdf
Description
D1843R00254_ENGAGE_SAP_RedactedPDFA
URL
http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7111&studyid=4399&filename=D1843R00254_ENGAGE_DM_CSP_redacted_PDFA.pdf
Description
D1843R00254_ENGAGE_Protocol_redactedPDFA
URL
http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7111&studyid=4399&filename=D1843R00254_ENGAGE_SAP_redacted.pdf
Description
D1843R00254_ENGAGE_SAP_RedactedPDFA

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ENhancing Outcomes Through Goal Assessment and Generating Engagement in Diabetes Mellitus

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