Type 2 Diabetes Mellitus Clinical Trial
Official title:
The Potential for Diet Modification to Improve Glycaemic Control and Cardiovascular Risk Factors Over and Above Drug Therapy in Type 2 Diabetes at High Risk of Cardiovascular Disease
In the past, nutritional management formed the cornerstone of treatment of type 2 diabetes (T2DM). More recently, this aspect of treatment has received less attention as drug therapy aimed not only to lower glucose, but also to treat raised blood pressure and blood fats (including cholesterol) has been more widespread. While there is evidence to suggest that blood pressure and blood fat levels have improved, overall diabetes control has not and people with diabetes appear to be becoming progressively more overweight, following trends in the general population. The proposed study involves a randomised controlled trial in which people with T2DM continuing with their regular drug treatment and surveillance, will be randomly allocated to additionally receive intensive advice regarding diet or remain on their usual treatment in this regard. The results will be judged principally in terms of body weight, waist circumference, blood pressure, blood glucose control and blood fats.
This is a 6-month pilot intervention study which seeks to determine whether adherence to an
intensive evidence based dietary programme, in addition to the prescription of both
cardioprotective and hypoglycaemic medications recommended for patients with diabetes, will
provide health benefits in terms of reducing the risk of developing or progression of
complications of diabetes (particularly cardiovascular disease).
The specific aim of the project is to compare the effects of an intensive lifestyle
intervention (based on the recently published evidence based recommendations of the
Nutrition Study Group of the European Association for the Study of Diabetes [3]) or usual
dietary advice, in diabetic patients at high risk of cardiovascular disease, treated with
cardioprotective and hypoglycaemic drugs.
Study participants will be randomised into two groups:
- The control group will receive usual dietary advice and diabetes treatment from their
usual GP and practice nurse (as detailed in the Management of Type 2 Diabetes and The
Assessment and Management of Cardiovascular Risk guidelines published in December 2003
[1,2]).
- In addition to usual care, the intervention group will receive intensive instruction
about a recommended dietary pattern based on the recently published recommendations of
the Nutrition Study Group of the European Association for the Study of Diabetes [3] and
where appropriate use material, for example serving size information from the above
mentioned guidelines.
Outcome will be determined by examining surrogate markers of clinical endpoints. These
surrogate markers will include clinical measures (weight, body mass index, blood pressure)
and appropriate tests (haemoglobin A1c, fasting insulin, blood lipids, lipoproteins,
inflammatory markers, and urine albumin creatinine ratio). A quality of life questionnaire
will also be administered at the beginning and end of the project.
1. New Zealand Guidelines Group. The assessment and management of cardiovascular risk.
Wellington, NZ. December, 2003. http://www.nzgg.org.nz
2. New Zealand Guidelines Group. Management of Type 2 diabetes. Wellington, NZ. December,
2003. http://www.nzgg.org.nz
3. Mann JI, De Leeuw I, Hermansen K, Karamanos B, Karlstrom B, Katsilambros N, Riccardi G,
Rivellese AA, Rizkalla S, Slama G, Toeller M, Uusitupa M, Vessby B. Nutr Metab
Cardiovasc Dis 14:373-394, 2004
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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