Intensive Care Unit-acquired muscle weakness (FITonICU)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Primary critical disease, meeting the diagnostic criteria for ICU acquired myasthenia; (2) The patient was hospitalized in ICU for 2 weeks with mechanical ventilation for more than 48 hours; (3) Aged 18-85; (4) lower extremity motor dysfunction; (5) Clear consciousness, good cardiopulmonary function, stable vital signs, able to cooperate well with training; (6) Promise to abide by the research procedures, cooperate with the whole process of the study and sign the informed consent; (7) Commit to follow the lifestyle considerations during the study.
Exclusion criteria
Exclusion criteria: (1) Lack of informed consent; (2) Patients with implanted pacemaker or defibrillator; (3) patients with unhealed fractures, severe osteoporosis and acute venous thrombosis; (4) Patients with severe hypertension (systolic blood pressure >200mmHg, diastolic blood pressure >110mmHg), diabetes with poor blood sugar control or complicated with serious diseases such as dysfunction of liver, kidney, heart and other important organs; (5) severe limited passive range of motion of hip, knee and ankle joints; (6) Refractory or multiple epilepsy; (7) severely impaired in vision, hearing or understanding; (8) participating in another clinical trial; (9) Known to have allergic reaction, hypersensitivity or intolerance to rehabilitation robots; (10) Any condition which, in the opinion of the investigator, is likely to prejudice the subject or cause the subject to fail to meet or perform the study requirements.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Muscle thickness of key muscles of lower limbs; | — |
Secondary
| Measure | Time frame |
|---|---|
| medical research council,MRC;modified barthel index,MBI;Measurement of lower limb circumference; | — |
Countries
China
Contacts
Shanghai Changhai Hospital