Type 2 Diabetes Clinical Trial
Official title:
Effects of Different Types of Exercise Interventions in Patients With Type 2 Diabetes - Aerobic Endurance Training Versus Strength Endurance Training Versus Combined Aerobic Endurance and Strength Endurance Training -
Verified date | April 2011 |
Source | University of Giessen |
Contact | n/a |
Is FDA regulated | No |
Health authority | Germany: Ethics Commission |
Study type | Interventional |
The purposes of the study are
- to determine which kind of supervised exercise intervention (aerobic endurance training
versus strength endurance training versus combined aerobic endurance and strength
endurance training) is more effective in improving the metabolic parameters in typ 2
diabetes patients
- to investigate what kind of intervention is more successful in reduction of concomitant
diseases and improving quality of life
- to assess what kind of intervention induces highest effects in long term persistence of
these positive changes
Status | Active, not recruiting |
Enrollment | 100 |
Est. completion date | June 2012 |
Est. primary completion date | November 2011 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - diagnoses of type 2 diabetes (ADA criteria) - admitted diabetes treatments will be diet and oral hypoglycemic agents Exclusion Criteria: - sports intervention >60 minutes per week - medical conditions - preproliferative or proliferative retinopathy - instable coronary heart disease - inability to perform the scheduled physical activity programs - acute clinically significant intercurrent diseases |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Germany | University of Giessen | Giessen | Hessen |
Germany | Sportpark Zwickau, Glauchau, Meerane | Zwickau | Sachsen |
Lead Sponsor | Collaborator |
---|---|
University of Giessen | Hannover Medical School |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in HbA1c-level (haemoglobin A1c) | 6 months | No | |
Secondary | Change in HOMA-Index | 3 and 6 months | No | |
Secondary | Change in beta-cell-function | Measured by OGTT (Oral Glucose Tolerance Test) | 3 and 6 months | No |
Secondary | Change in fasting plasma glucose levels | 3 and 6 months | No | |
Secondary | Change in total cholesterol levels | 3 and 6 months | No | |
Secondary | Change in HDL-cholesterol levels | 3 and 6 months | No | |
Secondary | Change in LDL-cholesterol levels | 3 and 6 months | No | |
Secondary | Change in triglyceride levels | 3 and 6 months | No | |
Secondary | Change in antidiabetic medications | Class and dosage of blood-glucose lowering drugs are recorded before, after 3 and 6 months | 3 and 6 months | No |
Secondary | Change in inflammation markers | CrP, blood count, interleukinstatus, cytokinstatus | 3 and 6 months | No |
Secondary | Change in body weight | 3 and 6 months | No | |
Secondary | Change in body composition | by Bio-impedance analysis, waist to hip ratio, range of thigh | 3 and 6 months | No |
Secondary | Change in strength | by Dr. Wolff Back Check | 3 and 6 months | No |
Secondary | Change of maximum heart rate | Measured by an incremental exercise test | 3 and 6 months | No |
Secondary | Change of peak oxygen uptake | Measured by an incremental exercise test | 3 and 6 months | No |
Secondary | Change of vAT (ventilatory anaerobic threshold) | Measured by an incremental exercise test | 3 and 6 months | No |
Secondary | Change in blood pressure | 3 and 6 months | No | |
Secondary | Change in renal function | Creatininlevel, Albuminlevel (urine), Telomere length | 3 and 6 months | No |
Secondary | Change in concentration | by d2-test | 3 and 6 months | No |
Secondary | Change in quality of life | by questionnaire: SF-12, EQ5 | 3 and 6 months | No |
Secondary | Change of nutrition | by questionnaire: FEV, FFQ | 3 and 6 months | No |
Secondary | Change in voluntary physical activity | meassured by pedometer (one week) | 3 and 6 months | No |
Secondary | Change of cardiac output by Impedance cardiography | by Task Force Monitor | 3 and 6 months | No |
Secondary | Change of barorezeptorsensitivity | by Task Force Monitor | 3 and 6 months | No |
Secondary | Change in carotid-Intima-Media-Thickness | 3 and 6 months | No | |
Secondary | Change in aortic pulse-wave velocity | 3 and 6 months | No | |
Secondary | Change in central aortic pressure | 3 and 6 month | No | |
Secondary | Change in endothelial dysfunction | 3 and 6 months | No | |
Secondary | Change of parodontitis | 3 and 6 months | No | |
Secondary | Follow up of all parameters mentioned above | Follow up after 12 months (6 months after completing the exercise intervention) without any supervised intervention | after 12 months | No |
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