Effects of Whole-body Vibration Therapy on Type 2 Diabetic Patients with and Without Polyneuropathy
- Conditions
- Type 2 DiabetesDiabetic Peripheral NeuropathyExercise
- Interventions
- Other: exercise with whole body vibration deviceOther: placebo exercise
- Registration Number
- NCT06033508
- Lead Sponsor
- Pamukkale University
- Brief Summary
The aim of this study is to show how whole body vibration training practiced for 12 weeks affects the levels of inflammatory biomarkers such as C reactive protein (CRP) and, interleukin-6 (IL-6), in Type 2 diabetic patients (T2DM) with and without peripheral neuropathy.
- Detailed Description
Volunteers with type 2 diabetes mellitus with and without peripheric neuropathy will be evaluated in terms of any contra-indication that will restrain them from making exercise with whole body vibration device. 60 male or female volunteers who are suitable in terms of inclusion/exclusion criteria will be invited for the study. Volunteers will be randomly distributed to one of the 3 groups. Each group will contain 20 participants. 1st group will include type 2 diabetic patients with peripheric neuropathy and 2nd and 3rd groups will include type 2 diabetic patients without neuropathy. Patients in group 1 and 2 will make static isometric exercises on vibration platform whereas patients in group 3 will make the same exercises on land in the hospital setting. Participants will be requested to complete 3 months of exercise. They will be evaluated before and at the end of the 3 months of exercise with physical measures such as waist and hip circumference, 6-minute walk test, body composition measured by bioimpedance, muscle thickness, and blood tests to measure inflammatory biomarkers.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 60
- Participants must stand and walk o without using an assistive device.
- Participants must have a weight of less than 120 kg.
- T2DM patients with advanced cardiovascular, renal, hepatic disease
- T2DM patients with diabetic retinopathy or nephropathy
- T2DM patients with untreated hypertension, rhythm disorders, and those who have undergone bypass surgery
- T2DM patients with ischemic changes in the resting ECG
- T2DM patients with untreated hypoglycemia or orthostatic hypotension
- T2DM patients who are unable to walk independently, or use of canes, crutches or wheelchairs
- T2DM patients who have open ulcers or wounds on load-bearing surfaces
- T2DM patients with inflammatory rheumatic diseases such as rheumatoid arthritis
- T2DM patients with active infectious disease
- T2DM patients with high risk of thrombosis, those with deep vein thrombosis
- T2DM patients who carry a pacemaker, prosthesis, intrauterine device or metal implant,
- T2DM patients with a history of cancer
- T2DM patients with severe migraine, epilepsy, stroke or other neurological disorders, those who have undergone brain surgery
- T2DM patients with non-diabetic neuropathy due to reasons such as HIV, AIDS, alcohol, uremia
- T2DM patients with cognitive impairment
- T2DM patients who are on psychotropic or neurotoxic therapy
- T2DM patients with advanced balance problems
- T2DM patients who are pregnant or breastfeeding mothers
- T2DM patients who are organ transplant recipients
- T2DM patients with hernia
- T2DM patients with kidney or bladder stones
- T2DM patients who are exposed to mechanical vibration due to their job
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description T2DM without neuropathy + WBV exercise with whole body vibration device Patients with type 2 Diabetes mellitus without neuropathy who will be trained by whole body vibration T2DM without neuropathy + land exercise placebo exercise Patients with type 2 Diabetes mellitus without neuropathy who will be trained on land T2DM with neuropathy + WBV exercise with whole body vibration device Patients with type 2 Diabetes mellitus with neuropathy who will be trained by whole body vibration
- Primary Outcome Measures
Name Time Method 6 min walk test 12 weeks
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Pamukkale University
🇹🇷Denizli, Turkey