Recruitment

Recruitment Status
Enrolling by invitation
Estimated Enrollment
Same as current

Summary

Conditions
  • Early Waking
  • ICU Acquired Weakness
  • Trauma
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Single (Outcomes Assessor)Primary Purpose: Treatment

Participation Requirements

Age
Between 20 years and 125 years
Gender
Both males and females

Description

Purpose: Trauma is often accompanied by injury-related neurological impairments, early physiological instabilities, and the use of high numbers of invasive catheters. Relatedly, patients with trauma have high rates of major disability and frequently require protracted rehabilitation with prolonged p...

Purpose: Trauma is often accompanied by injury-related neurological impairments, early physiological instabilities, and the use of high numbers of invasive catheters. Relatedly, patients with trauma have high rates of major disability and frequently require protracted rehabilitation with prolonged periods of recovery. Recently, it has been found that the use of progressive early mobilization (EM) protocols may minimize the functional declines experienced by patients in general during intensive care unit (ICU) stays, but few studies have investigated the effects of such protocols on trauma patients in particular. In addition, prior early mobilization studies have found that the survivors of trauma often experience a greater incidence of neurological injuries than other critical care patients. However, no randomized controlled trials thus far have utilized objective evaluations to measure the influence or effect of progressive EM protocols on the functional recovery of trauma patients. Therefore, we aim to explore the effects of using a progressive EM protocol in a trauma ICU on the functional mobility of trauma patients. Objective: The goals of this proposed research study are (1) to investigate the feasibility of using a structured progressive EM protocol for patients with trauma in a trauma ICU and (2) to determine the effectiveness of the progressive EM protocol, which is designed for implementation with trauma patients, on the functional and in-body outcomes of such patients. Research methods: The study will be a single-blind, randomized controlled trial with a blinded assessment at the end of the follow-up period.

Tracking Information

NCT #
NCT04810273
Collaborators
Not Provided
Investigators
Principal Investigator: Wen-Shiang Chen, Ph.D Department of Physical Medicine and Rehabilitation