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Empowerment, Motivation and Medical Adherence (EMMA). (EMMA)

Primary Purpose

Type2 Diabetes Mellitus

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
EMMA
Treatment as Usual
Sponsored by
Nova Scotia Health Authority
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Type2 Diabetes Mellitus

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Adults with type 2 diabetes ≥ 18 years
  • Type 2 diabetes ≥ 1 years
  • HbA1c ≥ 8 % at the last three visits before randomization
  • On oral or injectable medications (insulin, GLP-1; DPP-4)
  • Can speak, read and understand English

Exclusion Criteria:

  • Participation in other clinical intervention studies during the trial period
  • Receiving psychological or psychiatric treatment for a mental health disorder
  • Severely impaired vision or blindness

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    EMMA

    Treatment as Usual

    Arm Description

    These participants will receive diabetes self-management education using the dialogue tools, which emphasize empowerment and use the principles of motivational communication and behaviour modification. There will be a series of four visits using the dialogue tools to guide the patient toward meaningful self-management tasks. This is not the typical approach, where providers tell the patient the behaviours they, not the patient, consider priorities. This intervention will evaluate if medical outcomes (A1c) and adherence are improved using a patient-centered not a clinician-cantered approach in individuals with poor diabetes control.

    The participants will receive standard diabetes education via group and individual sessions with certified diabetes educators. In this method the patient is provided structured education in which there is an emphasis on covering clinician-determined aspects of diabetes knowledge and self-management. The emphasis vis on diabetes educator recommendations.

    Outcomes

    Primary Outcome Measures

    Hemoglobin A1c
    Hemoglobin A1c is a blood test that is considered to be the gold standard of diabetes control

    Secondary Outcome Measures

    WHO-QoL Scale
    The validated WHO quality of life self-report index will be used to assess quality of life
    Support for autonomous control over diabetes
    The validated Healthcare Climate Questionnaire (HCCQ), measures the support for autonomy from healthcare professionals experienced by the patient
    Self-management of diabetes
    The validated self-report scale, Treatment Self-Regulation Questionnaire (TSRQ), measures the patient's motivation for health behaviour change
    Self-Efficacy at diabetes self-management
    The validated self-report scale, the Perceived Competence in Diabetes (PCD), measures the patient's experience of competence in diabetes self-management
    Diabetes Distress
    The validated scale, the Diabetes Distress Scale (DDS) measures the experience of the burden of diabetes in everyday life

    Full Information

    First Posted
    December 29, 2016
    Last Updated
    August 1, 2018
    Sponsor
    Nova Scotia Health Authority
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03008395
    Brief Title
    Empowerment, Motivation and Medical Adherence (EMMA).
    Acronym
    EMMA
    Official Title
    Empowerment, Motivation and Medical Adherence (EMMA). Dialogue Tools for Consultations With Patients With Type 2 Diabetes
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2018
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Unable to secure clinic support for conducting research
    Study Start Date
    October 2017 (Anticipated)
    Primary Completion Date
    August 2018 (Anticipated)
    Study Completion Date
    August 2018 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Nova Scotia Health Authority

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Outcomes in type 2 diabetes are largely achieved by self-management efforts by individuals living with diabetes. Diabetes self-management is typically provided using the principles of adult education. Current evidence suggests that standard educational interventions are suboptimal. This study evaluates a novel approach to diabetes self-management using dialogue tools based on empowerment and motivational communication methods. The approach evaluated in this study is called EMMA: empowerment, motivation and medical adherence. Participants will be randomized to EMMA and treatment as usual, treated for a period of 4 months and evaluated over a period of 12 months.
    Detailed Description
    The management of type 2 diabetes (T2D) is experienced by many patients as being very complex. This is especially true when diabetes management includes multiple medical interventions such as oral agents and injectable medication (insulin, GLP-1; DPP-4s) in combination with diabetes specific behaviours such as blood glucose monitoring and foot care as well as healthy lifestyle behaviours such as physical activity and healthy eating. Studies show that 40-50 % of patients with T2D have suboptimal adherence to self-management recommendations. In general, it is estimated that about half of patients with chronic diseases do not take their medications as prescribed. Suboptimal medical adherence drives poor glycemic control as well as poor quality of life for an individual patient not to mention increased health care costs due to comorbidities, reduced work function and hospital admissions. Suboptimal adherence may be driven by numerous factors, including lack of symptoms of TD2 (perceived nonseriousness of the disease), side-effects of treatments (GI distress associated with metformin, weight gain associated with insulin) in conjunction with a complex dosing regimen, lack of knowledge or belief in the efficiency of the medication, lack of motivation, cultural factors as well as poor instruction and judgmental communication between the healthcare professional and patient. There is a need for new methods to understand the drivers of nonadherence and support the patient to proactively self-manage their TD2. There is also a need for new tools (i.e., knowledge translation methods) to support healthcare professionals to engage patients based on dialogue (collaboration) and active patient involvement (self-management), to overcome the barriers to adherence and thereby improve their ability to obtain good glycemic control. The purpose of this study is to evaluate a self-management support intervention called EMMA: Empowerment, motivation & medical adherence. EMMA is a concept consisting of a number of dialogue tools for use in diabetes consultations (see below). The concept was, in its original form tested, in a feasibility study (N = 19 T2D) in 2011-12. The study showed significant reduction in HbA1c (EMMA: median decrease of 2.0 mmol / mol (-1.0 to 3.0) versus control: median increase 2.5 mmol / mol (-2.0 to -4.5) p = 0.05) (Varming 2012; Andrésdóttir 2014). The investigators have been collaborating with the Danish group who have developed the EMMA protocol and have developed training programs to support the diabetes educator in the delivery of the intervention. The use of the EMMA method is very consistent with motivational communication and behaviour change counselling. The investigators plan to conduct a small scale randomized comparison trial of the EMMA method with diabetes services at the NSHA Central Zone.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Type2 Diabetes Mellitus

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    EMMA
    Arm Type
    Experimental
    Arm Description
    These participants will receive diabetes self-management education using the dialogue tools, which emphasize empowerment and use the principles of motivational communication and behaviour modification. There will be a series of four visits using the dialogue tools to guide the patient toward meaningful self-management tasks. This is not the typical approach, where providers tell the patient the behaviours they, not the patient, consider priorities. This intervention will evaluate if medical outcomes (A1c) and adherence are improved using a patient-centered not a clinician-cantered approach in individuals with poor diabetes control.
    Arm Title
    Treatment as Usual
    Arm Type
    Active Comparator
    Arm Description
    The participants will receive standard diabetes education via group and individual sessions with certified diabetes educators. In this method the patient is provided structured education in which there is an emphasis on covering clinician-determined aspects of diabetes knowledge and self-management. The emphasis vis on diabetes educator recommendations.
    Intervention Type
    Behavioral
    Intervention Name(s)
    EMMA
    Intervention Description
    Dialogue tools will be used to develop personally relevant behavioural goals consistent with diabetes self-management
    Intervention Type
    Other
    Intervention Name(s)
    Treatment as Usual
    Other Intervention Name(s)
    Standard Diabetes Education
    Intervention Description
    Participants randomized to this intervention will receive standard diabetes education sessions. These include group education session and follow up session based on clinician-generated recommendations.
    Primary Outcome Measure Information:
    Title
    Hemoglobin A1c
    Description
    Hemoglobin A1c is a blood test that is considered to be the gold standard of diabetes control
    Time Frame
    12 months
    Secondary Outcome Measure Information:
    Title
    WHO-QoL Scale
    Description
    The validated WHO quality of life self-report index will be used to assess quality of life
    Time Frame
    12 months
    Title
    Support for autonomous control over diabetes
    Description
    The validated Healthcare Climate Questionnaire (HCCQ), measures the support for autonomy from healthcare professionals experienced by the patient
    Time Frame
    12 months
    Title
    Self-management of diabetes
    Description
    The validated self-report scale, Treatment Self-Regulation Questionnaire (TSRQ), measures the patient's motivation for health behaviour change
    Time Frame
    12 Months
    Title
    Self-Efficacy at diabetes self-management
    Description
    The validated self-report scale, the Perceived Competence in Diabetes (PCD), measures the patient's experience of competence in diabetes self-management
    Time Frame
    12 Months
    Title
    Diabetes Distress
    Description
    The validated scale, the Diabetes Distress Scale (DDS) measures the experience of the burden of diabetes in everyday life
    Time Frame
    12 Months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Adults with type 2 diabetes ≥ 18 years Type 2 diabetes ≥ 1 years HbA1c ≥ 8 % at the last three visits before randomization On oral or injectable medications (insulin, GLP-1; DPP-4) Can speak, read and understand English Exclusion Criteria: Participation in other clinical intervention studies during the trial period Receiving psychological or psychiatric treatment for a mental health disorder Severely impaired vision or blindness
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Michael Vallis, PhD
    Organizational Affiliation
    Lead, Behaviour Change Institute, NSHA and Associate Professor, Family Medicine, Dalhousie University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
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