Effect of Alter-G Training on Glycemic Control and Quality of Life in Diabetic Neuropathy
Diabetic Polyneuropathy
About this trial
This is an interventional treatment trial for Diabetic Polyneuropathy focused on measuring Diabetic neuropathy,Quality of Life,Blood Glucose,Glycated Hemoglobin
Eligibility Criteria
Inclusion Criteria:
- Participants with diabetic polyneuropathy,
- Diagnosed as having uncontrolled type 2 diabetes mellitus, with glycosylated hemoglobin (HbA1c) value between 7 and 11 and fasting glucose level ranged from 7.0 -11.1 mmol/L,
- Age range from 60 and 80 years old,
- Established type 2 diabetes mellitus duration over 10 years, treated only with oral anti-diabetic agents (not taking insulin), treated only with Biguanide alone or (Sulfonylureas plus Biguanide) oral anti-diabetic drugs combination, with pharmacological treatment had to be stable for at least 3 months before the study,
- Cognitively competent and able to understand and follow instructions, capable of rationally interacting with others; understanding and answering the health related quality of life questionnaire (HRQL).
Exclusion Criteria:
- Type 1 DM, treated with insulin therapy or oral anti-diabetic therapy other than Biguanide alone or (Sulfonylureas plus Biguanide) combination,
- Younger than 60 or older than 80 years old,
- Patient with malnutrition (BMI < 21 kg/m2 or with recent weight loss > 5% body weight in the last month or > 10% in six months),
- Patients with established hypertension (resting systolic blood pressure > 140 mmHg and diastolic blood pressure > 90 mmHg,
- Active infection, drug abuse, participated in to an active rehabilitation program within last 6 months,
- With severe chronic or uncontrolled comorbid condition as recent myocardial infarction, unstable angina, acute congestive heart failure, third degree heart block and uncontrolled arrhythmia.
- With abnormal skin integrity e.g. wound or scares tissues or are on other complementary treatment,
- History of serious cerebrovascular or cardiovascular diseases, and severe debilitating musculoskeletal problems) that could interfere with the evaluation or treatment efficacy and patient safety or precluded the patient from attending and completing the treatment sessions.
Sites / Locations
- Umm Al-Qura University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Experimental
Experimental
Experimental
Experimental
No Intervention
"Zero percentage" weight off-loading group-A
"Twenty-five percentage" weight off-loading group-B
"Fifty percentage" weight off-loading group-C
"Seventy-five percentage" weight off-loading group-D
Control group-E
This group received the Mild to moderate aerobic exercise training on the Alter-G treadmill with the full weight-bearing for three months.
This group received the Mild to moderate aerobic exercise training on the Alter-G treadmill with the twenty-five percentage" weight off-loading for three months.
This group received the Mild to moderate aerobic exercise training on the Alter-G treadmill with the fifty percentage" weight off-loading for three months.
This group received the Mild to moderate aerobic exercise training on the Alter-G treadmill with the seventy-five percentage" weight off-loading for three months.
Participated no aerobic exercise training.