type 2 diabetes mellitus with overweight or obesity
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ? Meeting WHO diagnostic criteria for type 2 diabetes; ? 25kg/m2 = BMI <35kg/m2 (WHO); ? HbA1c between 6.5 and 11% in the last 3 months; ? Basic glucose-lowering treatment regimen without injectable insulin promoters, insulin; ? 55-70 years old, 50/50 male and female (6 males and 6 females); ? No physician-emphasized contraindications to exercise (e.g., severe heart disease, arthritis, limb disorders, osteoporosis, history of fracture, etc.), with the ability to care for themselves and basic exercise capacity; ? No metal grafts, etc. in the body; ? Agree to participate in three energy metabolism chamber test experiments.
Exclusion criteria
Exclusion criteria: ? Uncontrolled hypertension (resting blood pressure = 160/100 mmHg); severe cardiovascular and cerebrovascular disease, respiratory disease, hepatic and renal insufficiency, malignancy and other chronic wasting diseases, active infection and a history of surgery involving vital organs in the past 3 months; ? Acute complications of diabetes (diabetic ketoacidosis, hyperosmolar state, infection) occurred in the past 3 months, or the presence of one or more serious chronic complications of diabetes, such as severe cardiovascular and cerebrovascular pathology (angina pectoris, myocardial infarction, grade III-IV heart failure, severe arrhythmias, transient ischemic attack, stroke, etc.), massive proteinuria (urinary albumin/creatinine ratio = 300 mg/g ), severe diabetic foot, severe neuropathy, blurred vision; ? Those who did not pass the pre-experimental mental status assessment (PHQ-9 , SAS, verbal questioning about the presence of claustrophobia). Those with depression, anxiety or claustrophobia, etc.; those with severe sleep disorders. Those taking psychotropic drugs or insomnia drugs; ? Those who participated in other clinical trial programs in the past 3 months or currently, those who participated in regular physical activity in the past 6 months (150 min of moderate-to-vigorous physical activity per week); ? Those whose weight loss within 3 months exceeded 5% of initial weight; ? Those who smoked daily and could not stop smoking (occasional smokers could be included), and those who drank alcohol daily and could not stop drinking (occasional drinkers could be included); ? Those who failed the pre-exercise risk screening and assessment (PAR-Q); Those who diagnosed by doctors as osteoporosis or fracture who are not suitable to participate in the exercise intervention program in this study; ? Those with language expression impairment as judged by the researcher through communication and unable to communicate with the testers outside the chamber with immediate signals.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| energy expenditure; | — |
Secondary
| Measure | Time frame |
|---|---|
| Dynamic glucose monitoring;heart rate;physical activity;blood pressure; | — |
Countries
China
Contacts
National Fitness and Scientific Exercise Research Center, China Institute of Sport Science