Stroke
Conditions
Interventions
Observation group:None
Sponsors
Shenzhen Second People's Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: (1) Meets diagnostic criteria for stroke; (2) Vital signs are stable; (3) Age > 18 years; (4) Duration of the disease is more than 48 hours and less than 6 months; (5) Understand and actively participate in the assessment and training program.
Exclusion criteria
Exclusion criteria: (1) Unstable vital signs: expected maximal heart rate 180 beats/min; new malignant arrhythmia; new myocardial infarction with new initiation of antiarrhythmic medication or evidence of myocardial infarction combined with electrocardiographic or myocardial enzyme profiles; blood pressure SBP>180 mm Hg or DBP>110 mm Hg MAP40 breaths/min; mechanical ventilation FiO2>=0.60 PEEP>=10 cmH2O; human-machine asynchrony; change in mechanical ventilation to assisted or pressure support mode; difficulty in maintaining a fixed artificial airway; (2) Progressive stroke; acute phase of stroke; transient ischemic attack; patients with history of traumatic brain injury, encephalitis, tuberculous meningitis, and other history of parenchymal and central nervous involvement; (3) Acute coronary syndrome, decompensated heart failure, uncontrolled severe arrhythmia (rapid atrial fibrillation, atrial flutter, paroxysmal ventricular tachycardia, etc.) or high degree of atrioventricular block, severe heart valve disease, hypertrophic obstructive cardiomyopathy, active myocarditis, pericarditis, and other serious cardiac diseases; (4) Those with severe hepatic or renal insufficiency, including glomerular filtration rate GFR = 200 U/L, or aspartate aminotransferase AST >=200 U/L; (5) Combination of other serious diseases, such as malignant tumor, chronic kidney disease end stage, mental disorder, severe malnutrition, etc; (6) Lower limb fracture not healed, severe osteoporosis; (7) Pregnant or lactating women; (8) Participating in other clinical trials of drugs or medical devices during the same period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood pressure levels at different bed angles; | — |
Secondary
| Measure | Time frame |
|---|---|
| Heart rate;Cardiac output;Subjective symptoms (dizziness, fatigue); | — |
Countries
China
Contacts
Public ContactMingchao Zhou, Lirong Wang
Shenzhen Second People's Hospital
Outcome results
None listed