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Clinical Trials/NCT01115205
NCT01115205
Completed
Not Applicable

Assessment of Feasibility and Efficacy of a Project Aimed to Improve Metabolic Control in Type 2 Diabetes Through Lifestyle Changes and Self-monitoring of Blood Glucose

Universita di Verona0 sites59 target enrollmentMarch 2006
ConditionsType 2 Diabetes

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Type 2 Diabetes
Sponsor
Universita di Verona
Enrollment
59
Primary Endpoint
Change in haemoglobin A1c (HbA1c) levels
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

The purpose of the study is to evaluate the impact of an exercise programme organized into supervised walking groups on metabolic control, functional capacity and overall quantity of physical activity in subjects with type 2 diabetes.

Detailed Description

Regular, moderate-intensity physical activity can attenuate hyperglycemia in subjects with type 2 diabetes. In addition, these programmes may favourably affect several other cardiovascular risk factors in these subjects. However, it still remains unclear how this evidence can be transferred into clinical practice, considering the very large number of diabetic patients and the characteristics of this population, made up predominantly of elderly, sedentary and overweight patients. In this regard, a realistic approach to this issue requires simple and easily available intervention models. Walking is a typical mild-moderate aerobic physical activity which is easy to organize and does not require specific skills or preliminary sophisticated medical evaluations. This activity could therefore fit well with the need of involvement of large numbers of patients in different logistic situations. However, it has been reported that, due to the low walking speed typical of type 2 diabetic subjects, self-paced walking is inadequate to obtain a significant metabolic improvement in these subjects.

Registry
clinicaltrials.gov
Start Date
March 2006
End Date
January 2009
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Universita di Verona

Eligibility Criteria

Inclusion Criteria

  • diabetes known for at least 2 yr
  • physical inactivity
  • haemoglobin (Hb)A1c between 6.5-9.9%
  • treatment with oral hypoglycaemic agents alone or associated with a bed-time insulin injection
  • willingness to participate in a programme of regular physical activity

Exclusion Criteria

  • moderate-severe autonomic or somatic neuropathy
  • severe lower limb vasculopathy
  • pre-proliferative or proliferative active retinopathy
  • moderate to severe chronic renal failure
  • unstable angina or recent (in the previous 3 months) myocardial infarction
  • acute intercurrent diseases
  • acute metabolic decompensation (blood glucose \>300 mg/dl or ketonuria in two consecutive checks)
  • use of beta-blocker drugs
  • subjects unable to complete a 6-min walk test

Outcomes

Primary Outcomes

Change in haemoglobin A1c (HbA1c) levels

Time Frame: 4 months

The measurement of HbA1c is carried out with a DCCT-aligned method.

Secondary Outcomes

  • Change in Blood Pressure(4 months)
  • Change in Fasting plasma glucose levels(4 months)
  • Change in HDL Cholesterol levels(4 months)
  • Change in Total Cholesterol levels(4 months)
  • Change in Antidiabetic medications(4 months)
  • Change in Body weight(4 months)
  • Change in Energy expenditure through voluntary physical activity(4 months)
  • Change in LDL Cholesterol levels(4 months)
  • Change in Triglycerides levels(4 months)
  • Change in 6 minutes walk distance(4 months)
  • Change in C-reactive protein levels(4 months)
  • Compliance with walking sessions(4 months)

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