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Early Mobility for the Critically Injured Burn Patient

Primary Purpose

Critically Injured Burn Patients

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Standardized Rehabilitation Therapy
Sponsored by
Wake Forest University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Critically Injured Burn Patients

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 years or older
  • Mechanically ventilated via an endotracheal tube or mask (via tracheostomy is acceptable if performed emergently due to burn injury)
  • Burn injury requiring ICU admission

Exclusion Criteria:

  • Inability to walk without assistance prior to burn injury (use of a cane or walkers not exclusions)
  • Cognitive impairment prior to burn injury (non-verbal)
  • Acute Stroke
  • Body Mass Index (BMI) >50
  • Neuromuscular disease that could impair ventilator weaning (myasthenia gravis, ALS, Gillian-Barre)
  • Hospitalization within 30 days prior to burn injury
  • Re-admission to ICU/BICU within current hospitalization
  • Expected hospitalization length of stay < 3 days
  • Hip fracture, unstable cervical spine or pathological fracture
  • Mechanically ventilated >80 hours prior to study enrollment
  • Current hospitalization or transferring hospital stay >7days prior to study enrollment
  • DNR/DNI on admission
  • Ineligible cancer treatment within the last 6 months
  • Investigator judgment/determination that patient is unable to participate in intervention (SRT)
  • Moribund
  • Participation in treatment arm of another research study within the past 30 days/or at any time during the treatment phase of this study

Sites / Locations

  • Washington University
  • University of North Carolina, Chapel-Hill
  • Wake Forest University Baptist Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Usual Care

Standardized Rehabilitation Therapy

Arm Description

Standardized Rehabilitation Therapy (SRT): Participants randomized to the Standardized Rehabilitation Therapy arm will receive three types of interventions - Passive Range of Motion (PROM), Physical Therapy (PT) and Progressive Resistance Exercise (PRE). The SRT protocol will be administered by the BICU Mobility Team within 80 hours of ventilation and contains four levels of activity therapy. This Protocol will be delivered 7 days a week. Patients will be assessed daily and if appropriate will receive 3 separate sessions of activity each day.

Outcomes

Primary Outcome Measures

Hospital length of stay

Secondary Outcome Measures

Functional Status & Health Related Quality of Life

Full Information

First Posted
May 21, 2013
Last Updated
May 29, 2018
Sponsor
Wake Forest University
Collaborators
United States Department of Defense, Washington University School of Medicine, University of North Carolina, Chapel Hill
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1. Study Identification

Unique Protocol Identification Number
NCT01866735
Brief Title
Early Mobility for the Critically Injured Burn Patient
Official Title
Early ICU Standardized Rehabilitation Therapy for the Critically Injured Burn Patient
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Terminated
Why Stopped
Results from trial in another population lead investigators to determine study outcome may not reach statistical significance.
Study Start Date
May 2013 (Actual)
Primary Completion Date
March 1, 2015 (Actual)
Study Completion Date
March 1, 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wake Forest University
Collaborators
United States Department of Defense, Washington University School of Medicine, University of North Carolina, Chapel Hill

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This study will demonstrate that Standardized Rehabilitation Therapy for burn patients with ARF reduces hospital stay through immediate improvement in functional capacity and functional performance. Our team comprises Burn Surgeons, Intensivists with expertise in Critical Care Trial design, Exercise Physiologists and Outpatient Functional Outcome Assessment Experts. The design was conceived through the US-Critical Illness and Injury Trials Group which allowed these investigators to bring varied expertise to the problems faced by critically ill Burn patients. Hypotheses:1) Standardized Rehabilitation Therapy (SRT) will shorten hospital stay in burn patients with ARF. 2) SRT will prevent loss in muscle size and loss of architecture during critical illness of severe burns. 3) SRT will improve objective functional measures and quality of life at 3, 6, 12, 24, and 36 months post-enrollment.
Detailed Description
Background: Burn injury requiring mechanical ventilation affects a high proportion of the 25,000 patients admitted to US Burn Centers every year. Patients with a burn injury and acute respiratory failure (ARF) experience deconditioning, muscle weakness, joint contractures, dyspnea, depression, and reduced health-related quality of life. Delivery of rehabilitative therapy (physical therapy) within the Burn Intensive Care Unit (BICU) for burn patients requiring mechanical ventilation is not uniform in its content, timing, or the acceptance of its safety. Our published data indicate that Standardized Rehabilitation Therapy, initiated in the ICU, is feasible and safe for Medical ICU patients. Data have shown reductions in hospital stay, and improvements in functional outcomes. Mechanistically, it is understood that patients with burns and concomitant ARF exhibit acute alterations of metabolism, with the resultant loss of muscle strength. This study will demonstrate that Standardized Rehabilitation Therapy for burn patients with ARF reduces hospital stay through immediate improvement in functional capacity and functional performance. Our team comprises Burn Surgeons, Intensivists with expertise in Critical Care Trial design, Exercise Physiologists and Outpatient Functional Outcome Assessment Experts. The design was conceived through the US-Critical Illness and Injury Trials Group which allowed these investigators to bring varied expertise to the problems faced by critically ill Burn patients. Objective/Hypotheses: 1) Standardized Rehabilitation Therapy (SRT) will shorten hospital stay in burn patients with ARF. 2) SRT will prevent loss in muscle size and loss of architecture during critical illness of severe burns. 3) SRT will improve objective functional measures and quality of life at 3, 6, 12, 24, and 36 months post-enrollment. Specific Aims: Aim 1: To determine whether standardized rehabilitation therapy for BICU patients requiring mechanical ventilation will decrease hospital length of stay. Aim 2: To determine by serial ultrasound and strength assessments whether standardized rehabilitation therapy decreases loss of biceps and quadriceps size, architecture and strength during critical illness of the severe burn patient. Aim 3: To determine whether standardized rehabilitation therapy will improve functional capacity and performance, and quality of life. Study Design: The investigators will conduct a two arm trial with stratified randomization in 150 burn patients with concomitant ARF to compare SRT, initiated while on mechanical ventilation in the ICU and administered throughout the hospitalization, vs. Usual Care (control). Standardized Rehabilitation Therapy will consist of: passive range of motion, physical therapy, and progressive resistance exercise (strength training). Our unique approach will provide an experienced Mobility Team (7days/week) consisting of a critical care nurse, physical therapist, and nursing assistant to administer this protocol at 3 University Hospital sites. The proposed study is a natural extension of our prior work, is multidisciplinary, is supported by extensive preliminary studies, and is innovative in its application of strength training techniques and in-hospital strength assessments. Relevance: Burn patients with ARF suffer for months after hospital discharge with weakness and decreased quality of life. This study will provide the information to prioritize and budget for the rehabilitation needs of burn patients with ARF by demonstrating that Standardized Rehabilitation Therapy, initiated in the ICU, reduces hospital length of stay with immediate and sustained improvement in function and quality of life for burn patients with ARF. Given that military burn patients and civilian burn patients utilize similar resources and experience similar outcomes, the results of this study will be immediately transferable to the military burn patient with concomitant ARF resulting in improved outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critically Injured Burn Patients

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Usual Care
Arm Type
No Intervention
Arm Title
Standardized Rehabilitation Therapy
Arm Type
Experimental
Arm Description
Standardized Rehabilitation Therapy (SRT): Participants randomized to the Standardized Rehabilitation Therapy arm will receive three types of interventions - Passive Range of Motion (PROM), Physical Therapy (PT) and Progressive Resistance Exercise (PRE). The SRT protocol will be administered by the BICU Mobility Team within 80 hours of ventilation and contains four levels of activity therapy. This Protocol will be delivered 7 days a week. Patients will be assessed daily and if appropriate will receive 3 separate sessions of activity each day.
Intervention Type
Other
Intervention Name(s)
Standardized Rehabilitation Therapy
Primary Outcome Measure Information:
Title
Hospital length of stay
Time Frame
From date of randomization through 36 months post-study enrollment
Secondary Outcome Measure Information:
Title
Functional Status & Health Related Quality of Life
Time Frame
ICU/Hospital Discharge, 3, 6 & 12 months post enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 years or older Mechanically ventilated via an endotracheal tube or mask (via tracheostomy is acceptable if performed emergently due to burn injury) Burn injury requiring ICU admission Exclusion Criteria: Inability to walk without assistance prior to burn injury (use of a cane or walkers not exclusions) Cognitive impairment prior to burn injury (non-verbal) Acute Stroke Body Mass Index (BMI) >50 Neuromuscular disease that could impair ventilator weaning (myasthenia gravis, ALS, Gillian-Barre) Hospitalization within 30 days prior to burn injury Re-admission to ICU/BICU within current hospitalization Expected hospitalization length of stay < 3 days Hip fracture, unstable cervical spine or pathological fracture Mechanically ventilated >80 hours prior to study enrollment Current hospitalization or transferring hospital stay >7days prior to study enrollment DNR/DNI on admission Ineligible cancer treatment within the last 6 months Investigator judgment/determination that patient is unable to participate in intervention (SRT) Moribund Participation in treatment arm of another research study within the past 30 days/or at any time during the treatment phase of this study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter E Morris, MD
Organizational Affiliation
University of Kentucky
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
James Holmes, MD
Organizational Affiliation
Wake Forest University Health Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington University
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63130
Country
United States
Facility Name
University of North Carolina, Chapel-Hill
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
Facility Name
Wake Forest University Baptist Medical Center
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27157
Country
United States

12. IPD Sharing Statement

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Early Mobility for the Critically Injured Burn Patient

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