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Treatment of Critical Illness Polyneuromyopathy (Do-It-Now)

Primary Purpose

Acute Respiratory Failure

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
intensive physical therapy
control group
Sponsored by
University of Colorado, Denver
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Respiratory Failure focused on measuring mechanical ventilation, acute respiratory failure, physical therapy, critical illness neuropathy, critical illness myopathy

Eligibility Criteria

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

Inclusion Criteria:

  • Acute respiratory failure requiring mechanical ventilation for at least four days.

Exclusion Criteria:

  • Recent myocardial infarction within the last 3 weeks, presence of signs or symptoms of unstable angina or history of unstable arrhythmias including ventricular tachycardia and atrial fibrillation (HR > 100 bpm).
  • Recent history of pulmonary embolism within the last six weeks.
  • History of severe aortic stenosis.
  • Presence of a dissecting aortic aneurysm.
  • Significant language barrier that would limit the ability to participate in the physical therapy program.
  • Patients who live greater than 45 miles from the University of Colorado Hospital.
  • Underlying disorder that makes it unlikely that the patient will survive 6 months.
  • Severe physical or cognitive impairment that would impair their ability to exercise.

Sites / Locations

  • Medical Center of Aurora
  • University of Colorado Denver
  • Rose Medical Center
  • Swedish Medical Center
  • St. Anthony Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Intensive physical therapy

control group

Arm Description

four week intervention of daily intensive physical therapy

Outcomes

Primary Outcome Measures

The Primary Outcome Variable for This Study Will be the Short Form of the Continuous Scale Physical Functional Performance Test (CS-PFP) Called the PFP-10
The CS-PFP-10 provides an overall score and scores for upper body strength, upper body flexibility, lower body strength, balance and coordination, and endurance. The test is used to assess an individual's overall capacity to carry out activities of daily living by measuring and quantifying 10 typical activities including sweeping a floor, transferring clothes from a washer to a dryer, and carrying groceries. Tasks are quantified using time alone, time and weight, and distance. This test provides a realistic and practical measure of movement capacity and ability to accomplish sustained activity. CS-PFP-10 scores are scored from 0 to 100, with higher scores indicating better function. If patients remained in the hospital or in a long-term care facility a the time of assessment, then received a score of 0. All tests were conducted in a standardized physical therapy laboratory by a physical therapist formally trained in conducting the CS-PFP-10 and blinded to group/arm assignment.

Secondary Outcome Measures

ICU-free Days
Number of ICU-free days at Day 28.
ICU Length of Stay
Median ICU length of stay through Day 28
Mechanical Ventilation Duration
The total number of ventilated days from hospital admission to extubation, death or discharge over the complete duration of study participation, up to 180 days.
Hospital Free Days
Hospital Length of Stay
The total number of hospital days during study participation, up to 180 days.
Discharged to Home
Percentage of subjects discharged to home from study hospital
Institution Free Days
Median number of days subjects were alive and free of hospitalization or living in a longer-term care, rehabilitation, or skilled nursing facility.
Institution Free Days
Median number of days subjects were alive and free of hospitalization or living in a long-term care, rehabilitation, or skilled nursing facility.

Full Information

First Posted
January 26, 2010
Last Updated
March 16, 2017
Sponsor
University of Colorado, Denver
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1. Study Identification

Unique Protocol Identification Number
NCT01058421
Brief Title
Treatment of Critical Illness Polyneuromyopathy
Acronym
Do-It-Now
Official Title
Randomized Trial of Intensive Physical Therapy for Patients With Acute Respiratory Failure
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
September 2009 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
October 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Colorado, Denver

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Acute respiratory failure is a heterogeneous disorder that results in more than 300,000 Americans requiring admission to an intensive care unit for invasive mechanical ventilatory support each year. Though acute respiratory failure is a pulmonary disorder, patients who survive their hospitalization are not limited by respiratory symptoms after discharge. Rather persistent neuromuscular weakness is the primary disorder that adversely alters their quality of life and ability to function on a daily basis. In this application the investigators plan to conduct a randomized clinical trial called the Do It Now study (Diagnosis and Treatment of Neuromuscular Weakness) to determine the effectiveness of an intensive physical therapy program for patients recovering from acute respiratory failure. This trial will establish the efficacy of the physical therapy programs that is currently performed for patients with acute respiratory failure in a non-evidence based manner across the United States.
Detailed Description
Acute respiratory failure is a heterogeneous disorder that results in more than 300,000 Americans requiring admission to an intensive care unit for invasive mechanical ventilatory support each year. Though acute respiratory failure is a pulmonary disorder, patients who survive are not limited by respiratory symptoms after discharge. Rather persistent neuromuscular weakness is the primary disorder that adversely affects their quality of life and ability to function on a daily basis. Weakness in these survivors is related to the development of critical illness polyneuromyopathy (CIPNM). Presently, there are no therapies to treat the estimated 110,000 acute respiratory failure survivors who have developed CIPNM each year. Based on the results of our national surveys of physical therapists and intensive care physicians, the utilization and types of physical therapy for patients recovering from acute respiratory failure with neuromuscular weakness varies significantly depending on the type of hospital and primary diagnosis of the patient. The investigators plan to perform a randomized clinical trial to determine the effectiveness of an intensive four week physical therapy program for patients with acute respiratory failure. This trial will determine the efficacy of the physical therapy programs that is currently performed in a non-evidence based manner for patients with acute respiratory failure across the United States. If successful, this study will pave the way for a larger multi-center clinical trial of intensive physical therapy for survivors of acute respiratory failure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Failure
Keywords
mechanical ventilation, acute respiratory failure, physical therapy, critical illness neuropathy, critical illness myopathy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intensive physical therapy
Arm Type
Experimental
Arm Description
four week intervention of daily intensive physical therapy
Arm Title
control group
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
intensive physical therapy
Intervention Description
four week course of daily intensive physical therapy
Intervention Type
Procedure
Intervention Name(s)
control group
Intervention Description
four weeks of routine physical therapy
Primary Outcome Measure Information:
Title
The Primary Outcome Variable for This Study Will be the Short Form of the Continuous Scale Physical Functional Performance Test (CS-PFP) Called the PFP-10
Description
The CS-PFP-10 provides an overall score and scores for upper body strength, upper body flexibility, lower body strength, balance and coordination, and endurance. The test is used to assess an individual's overall capacity to carry out activities of daily living by measuring and quantifying 10 typical activities including sweeping a floor, transferring clothes from a washer to a dryer, and carrying groceries. Tasks are quantified using time alone, time and weight, and distance. This test provides a realistic and practical measure of movement capacity and ability to accomplish sustained activity. CS-PFP-10 scores are scored from 0 to 100, with higher scores indicating better function. If patients remained in the hospital or in a long-term care facility a the time of assessment, then received a score of 0. All tests were conducted in a standardized physical therapy laboratory by a physical therapist formally trained in conducting the CS-PFP-10 and blinded to group/arm assignment.
Time Frame
1 month
Secondary Outcome Measure Information:
Title
ICU-free Days
Description
Number of ICU-free days at Day 28.
Time Frame
Day 28
Title
ICU Length of Stay
Description
Median ICU length of stay through Day 28
Time Frame
Total Days through Day 28
Title
Mechanical Ventilation Duration
Description
The total number of ventilated days from hospital admission to extubation, death or discharge over the complete duration of study participation, up to 180 days.
Time Frame
up to 180 days
Title
Hospital Free Days
Time Frame
Through Day 28
Title
Hospital Length of Stay
Description
The total number of hospital days during study participation, up to 180 days.
Time Frame
up to 180 days
Title
Discharged to Home
Description
Percentage of subjects discharged to home from study hospital
Time Frame
Through Day 28
Title
Institution Free Days
Description
Median number of days subjects were alive and free of hospitalization or living in a longer-term care, rehabilitation, or skilled nursing facility.
Time Frame
At Day 90
Title
Institution Free Days
Description
Median number of days subjects were alive and free of hospitalization or living in a long-term care, rehabilitation, or skilled nursing facility.
Time Frame
Day 180

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Acute respiratory failure requiring mechanical ventilation for at least four days. Exclusion Criteria: Recent myocardial infarction within the last 3 weeks, presence of signs or symptoms of unstable angina or history of unstable arrhythmias including ventricular tachycardia and atrial fibrillation (HR > 100 bpm). Recent history of pulmonary embolism within the last six weeks. History of severe aortic stenosis. Presence of a dissecting aortic aneurysm. Significant language barrier that would limit the ability to participate in the physical therapy program. Patients who live greater than 45 miles from the University of Colorado Hospital. Underlying disorder that makes it unlikely that the patient will survive 6 months. Severe physical or cognitive impairment that would impair their ability to exercise.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marc Moss, M.D.
Organizational Affiliation
University of Colorado, Denver
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical Center of Aurora
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80012
Country
United States
Facility Name
University of Colorado Denver
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
Facility Name
Rose Medical Center
City
Denver
State/Province
Colorado
ZIP/Postal Code
80220
Country
United States
Facility Name
Swedish Medical Center
City
Englewood
State/Province
Colorado
ZIP/Postal Code
80113
Country
United States
Facility Name
St. Anthony Hospital
City
Lakewood
State/Province
Colorado
ZIP/Postal Code
80228
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
We have created a de-identified data set that is available to other investigators upon request.
Citations:
PubMed Identifier
28732512
Citation
Neumeier A, Nordon-Craft A, Malone D, Schenkman M, Clark B, Moss M. Prolonged acute care and post-acute care admission and recovery of physical function in survivors of acute respiratory failure: a secondary analysis of a randomized controlled trial. Crit Care. 2017 Jul 21;21(1):190. doi: 10.1186/s13054-017-1791-1.
Results Reference
derived
PubMed Identifier
26651376
Citation
Moss M, Nordon-Craft A, Malone D, Van Pelt D, Frankel SK, Warner ML, Kriekels W, McNulty M, Fairclough DL, Schenkman M. A Randomized Trial of an Intensive Physical Therapy Program for Patients with Acute Respiratory Failure. Am J Respir Crit Care Med. 2016 May 15;193(10):1101-10. doi: 10.1164/rccm.201505-1039OC.
Results Reference
derived

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Treatment of Critical Illness Polyneuromyopathy

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