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Effect of In-Patient Exercise Training on Length of Hospitalization in Burned Patients (MP-10)

Primary Purpose

Muscle Weakness, Late Effect of Burn, Muscle; Fatigue, Heart

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Exercise + SOC PT/OT
SOC PT/OT
Sponsored by
The University of Texas Medical Branch, Galveston
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Muscle Weakness focused on measuring Burn, Exercise, Ergometer, MP-10

Eligibility Criteria

7 Years - 60 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Male and female subjects ≥7 to 60 years of age
  2. >30% TBSA burned, as estimated by the physician in charge
  3. No evidence of organ failure

Exclusion Criteria:

  1. Active Tuberculosis- based on clinical symptoms and/or abnormal chest x-ray in the upper lobe.
  2. Electrical burns
  3. Mental retardation or autism or any other mental disorder that makes it impossible to participate in an exercise program
  4. Pregnancy

Sites / Locations

  • University of California-Davis/Shriners Hospitals for Children-Sacramento
  • University of Texas Southwestern Medical Center
  • University of Texas Medical Branch/Shriners Hospitals for Children-Galveston (lead site)
  • United States Army Institute of Surgical Research

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Exercise + SOC PT/OT

SOC PT/OT

Arm Description

SOC treatment plus a personalized, structured, and quantifiable exercise program (MP10) carried out soon after admission until hospital discharge (including during the BICU stay and time on ventilation.

Only SOC for treating in-patient burn subjects

Outcomes

Primary Outcome Measures

change in lean muscle mass
Kilograms

Secondary Outcome Measures

change in VO2 max
The maximal amount of oxygen per kilogram of body mass per minute(ml/kg/min) in a cardiopulmonary exercise test.
change in distance walked over 6 minutes
6 min walk test measures distance will be recorded in feet.

Full Information

First Posted
March 12, 2015
Last Updated
November 4, 2020
Sponsor
The University of Texas Medical Branch, Galveston
Collaborators
United States Army Institute of Surgical Research, University of Texas Southwestern Medical Center, California State University, Sacramento
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1. Study Identification

Unique Protocol Identification Number
NCT02739464
Brief Title
Effect of In-Patient Exercise Training on Length of Hospitalization in Burned Patients
Acronym
MP-10
Official Title
Randomized, Controlled, Multicenter Study of the Effect of In-Patient Exercise Training on Length of Hospitalization, Mental Health, and Physical Performance in Burned Patients
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
September 15, 2014 (Actual)
Primary Completion Date
September 25, 2020 (Actual)
Study Completion Date
September 25, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Texas Medical Branch, Galveston
Collaborators
United States Army Institute of Surgical Research, University of Texas Southwestern Medical Center, California State University, Sacramento

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will measure efficacy of early in-patient exercise as an adjunct to current Standard of Care (SOC) for 96 patients in a multi-centre trial. The secondary purpose is to assess the efficacy of a personalized, structured, and quantifiable exercise program (MP10) carried out soon after admission until hospital discharge (including during the BICU stay and time on ventilation).
Detailed Description
After severe burns (≥ 30% total body surface area [TBSA] burns, patients enter a persistent and extensive hypermetabolic and catabolic state. Unfortunately, burn-induced muscle catabolism is exacerbated by the prolonged bed rest and inactivity that accompanies hospitalization, leading to further loss of muscle mass and extreme weakness. The persistence of weakness, fatigue, and muscle catabolism from prolonged bed rest and inactivity during the acute care stage ultimately delays rehabilitation and return to normal physical activities. Studies conducted in non-burn patients have shown that, aside from decreasing muscle mass, prolonged bed rest has a host of other negative physiological consequences. The primary purpose of this randomized, controlled, multicenter study is being conducted to determine the efficacy of early in-patient exercise, when used as an adjunct to standard of care (SOC), in improving recovery of adults from burns. The secondary purpose is to assess the efficacy of a personalized, structured, and quantifiable exercise program (hereafter referred to as MP10) carried out soon after admission until hospital discharge (including during the BICU stay and time on ventilation). This objective will be met through a multicenter trial in children and adults (7 - 60 years) with ≥30% TBSA burns. Outcome variables will include BICU days, ventilator days, hospital days, peak treadmill time, and lean body mass and psychosocial function (See Section 8 for details). Methods: Ninety-six subjects will be recruited from four sites (24 subjects each) for this study and all genders and ethnicities will be invited. All subject will have TBSA > 30% and be ages 7-60 years of age. The first objective of this multicenter study will be to characterize the SOC related to physical/occupational therapy of inpatients at four U.S. burn centers, through 25 question surveys. The second portion of the project will involve exercise research. The objective is to assess the efficacy of MP10, in conjunction with existing SOC, in reducing debilitation among discharged burn patients. This will be initiated following surgeon's prescription, roughly 3-5 days following the first surgery after admission. Ergonomic exercise training for the in-patient subjects will be conducted using Leg and Arm Ergometer equipment, and the training period will be daily for 10 minutes. The duration will be the duration the patient is held in the Burn Intensive Care Unit (BICU). Testing will include the following: Lean mass (assessed via dual energy x-ray absorptiometry (DEXA), Cardiopulmonary and muscle endurance test (peak VO2 on treadmill test), and weekly 6 minute walk test. Data Analysis: A repeated measure ANOVA will be calculated using lean body mass and peak VO2 as dependent variables with the independent variables of TBA%, duration of hospital stay (and days of ergonomic exercise), ventilator days, and demographics. The purpose of this study is to measure efficacy of exercise training while in BICU for thermal injury patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Muscle Weakness, Late Effect of Burn, Muscle; Fatigue, Heart, Burn Rehabilitation
Keywords
Burn, Exercise, Ergometer, MP-10

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
77 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise + SOC PT/OT
Arm Type
Experimental
Arm Description
SOC treatment plus a personalized, structured, and quantifiable exercise program (MP10) carried out soon after admission until hospital discharge (including during the BICU stay and time on ventilation.
Arm Title
SOC PT/OT
Arm Type
Active Comparator
Arm Description
Only SOC for treating in-patient burn subjects
Intervention Type
Other
Intervention Name(s)
Exercise + SOC PT/OT
Intervention Type
Other
Intervention Name(s)
SOC PT/OT
Primary Outcome Measure Information:
Title
change in lean muscle mass
Description
Kilograms
Time Frame
It is the change from baseline until discharge. Baseline is the time in the ICU, approximately 1-3 months post burn. Discharge is within 3 weeks of the discharge date from the burn ICU. Study duration is at most 5 months depending on the patients burn.
Secondary Outcome Measure Information:
Title
change in VO2 max
Description
The maximal amount of oxygen per kilogram of body mass per minute(ml/kg/min) in a cardiopulmonary exercise test.
Time Frame
It is the change from baseline until discharge. Baseline is the time in the ICU, approximately 1-3 months post burn. Discharge is within 3 weeks of the discharge date from the burn ICU. Study duration is at most 5 months depending on the patients burn.]
Title
change in distance walked over 6 minutes
Description
6 min walk test measures distance will be recorded in feet.
Time Frame
It is the change from baseline until discharge. Baseline is the time in the ICU, approximately 1-3 months post burn. Discharge is within 3 weeks of the discharge date from the burn ICU. Study duration is at most 5 months depending on the patients burn.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male and female subjects ≥7 to 60 years of age >30% TBSA burned, as estimated by the physician in charge No evidence of organ failure Exclusion Criteria: Active Tuberculosis- based on clinical symptoms and/or abnormal chest x-ray in the upper lobe. Electrical burns Mental retardation or autism or any other mental disorder that makes it impossible to participate in an exercise program Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Oscar Suman
Organizational Affiliation
University of Texas Medical Branch/Shriners Hospital for Children
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California-Davis/Shriners Hospitals for Children-Sacramento
City
Davis
State/Province
California
ZIP/Postal Code
95616
Country
United States
Facility Name
University of Texas Southwestern Medical Center
City
Dallas
State/Province
Texas
ZIP/Postal Code
75390
Country
United States
Facility Name
University of Texas Medical Branch/Shriners Hospitals for Children-Galveston (lead site)
City
Galveston
State/Province
Texas
ZIP/Postal Code
77550
Country
United States
Facility Name
United States Army Institute of Surgical Research
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78234
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
ONLY de-identified data will be deposited with main site (UTMB). Subsequently, if data is shared among all sites, it will be always in de-identified manner and stripped of all information that could identify the participant.
IPD Sharing Time Frame
Data will become available once study is completed and 7 years after that date, according to the IRB standards.
IPD Sharing Access Criteria
Once study personnel has completed CITI training and add to the study, will they have access to the data.
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Effect of In-Patient Exercise Training on Length of Hospitalization in Burned Patients

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