Lifestyle Intervention For Effective Diabetes Management (LIFE-DM)
Diabetes Mellitus, Type 2
About this trial
This is an interventional supportive care trial for Diabetes Mellitus, Type 2 focused on measuring Diabetes, Lifestyle Intervention, Cardiovascular risk reduction
Eligibility Criteria
Inclusion Criteria:
- Type 2 Diabetes
- Age 18 years or older
Exclusion Criteria:
- Documented history of myocardial infarction, stroke, angina, angioplasty, or bypass surgery
- Unable to understand written and spoken English
- Presence of cognitive impairment (e.g., dementia) or significant psychological problems (e.g., schizophrenia, schizoaffective disorders) that, in the investigators' opinion, may prohibit the participant from following study protocols
- Unavailable to participate (e.g., incarceration, no access to a telephone)
- HIV / AIDS
- Estimated life expectancy less than one year in the opinion of the clinician
- Participation in any other clinical study
Sites / Locations
- St. Michael's Hospital
- University Health Network, Toronto Western Hospital
- St. Joseph's Health Centre
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
INTERxVENT Program
Usual medical care
Participants in INTERxVENT will complete a 'Baseline Assessment' and 'Follow-up' questionnaire, and will have a health professional visit his/her home for an initial assessment (BP,height,weight,waist measurement) and blood collection (blood glucose and cholesterol levels). As part of the program, each participant will also complete a self-reported 'Health History Questionnaire' (HHQ); a follow-up HHQ will be completed about 12 weeks into the program to monitor progress. Each participant randomized to INTERxVENT receives educational articles which address diabetes management issues. A structured, individualized program, consisting of educational materials and 12 live mentoring/coaching telephone calls will take place over 6 months. The mentors consist of allied health professionals. The sequence by which educational content is administered will be both self-directed and guided by the mentors using an algorithmic approach according to the participant's readiness-to-change scores.
Each participant randomized to this group will not receive any formal intervention but will receive the same care over the 6-month period as he/she usually receives from his/her health care team. Participants in this group will undergo the same baseline and outcome assessment as those in the intervention group, including blood pressure (BP) measurement, physical assessment (height, weight, waist measurement) and blood collection (blood glucose and cholesterol levels), as well as completion of the 'Baseline Assessment' and 'Follow-up' questionnaires.