Effect of vibration therapy on physical function in critically ill adults (VTICIA trial)
- Conditions
- Critically ill patients
- Registration Number
- JPRN-UMIN000039616
- Lead Sponsor
- The university of Tokushima
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 188
Not provided
We will exclude patients based on the consensus for early mobilization in the Japanese society of intensive care medicine (JSICM) as following: (1) no permission from the primary doctor (2) excessive agitation (RASS more than or equal to 2) (3) impaired consciousness (RASS less than or equal to 3) (4) Unstable vital sign requiring circulatory support devices such as intra-aortic balloon pump (5) sustained low blood pressure even with the use of catecholamine (6) dramatic blood pressure change after body position change (7) the risk of rupture in untreated aneurysms (8) uncontrolled pain 9) uncontrolled intracranial pressure more than or equal to 20 mmHg (10) unstable phase in head or cervical spine injury (11) unstable bone fracture (12) active bleeding (13) insufficient stabilization or length of catheters (14) insufficient staffing (15) no consent from patients or surrogates.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Functional Status Score for the ICU (FSS-ICU) at the discharge from the IC
- Secondary Outcome Measures
Name Time Method Delirium, Medical research council (MRC) score, the incidence of intensive care unit-acquired weakness (ICU-AW), ICU mobility scale (IMS), ventilator and ICU free days