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Clinical Trial Summary

We hypothesized that early exercise rehabilitation for patients with severe sepsis or septic shock would decrease their functional disability and cognitive impairment. We plan to enroll patients with severe sepsis and septic shock who admitted an urban teaching hospital in Seoul, South Korea via ER. We will randomize those subjects into the intervention group which will take a standardized rehabilitation with routine clinical care for sepsis and the control group which will take routine clinical care for sepsis. And, we plan to assess their functional activity using ADL, IADL and SF-36, and cognitive function using MMSE at the time of enrollment, 28 days, and 6 months later.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT01845766
Study type Interventional
Source Yonsei University
Contact
Status Completed
Phase N/A
Start date February 2013
Completion date November 2014

See also
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Completed NCT01689441 - Randomized Controlled Trial of Calcitriol vs. Placebo Among Critically-ill Patients With Sepsis Phase 2
Completed NCT02656654 - COrporeal Compression at the ONset of Severe Sepsis and Septic Shock N/A