search
Back to results

Assessing The Effects of Exercise, Protein, and Electric Stimulation On Intensive Care Unit Patients Outcomes (ExPrEs)

Primary Purpose

Muscle Weakness, Critical Illness, Sarcopenia

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MPR and High Protein Supplement (HPRO) and Neuromuscular Electric Stimulation (NMES)
Sponsored by
University of Maryland, Baltimore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Muscle Weakness focused on measuring Nutritional supplementation, Neuromuscular Electric Stimulation, ICU acquired weakness, Post ICU Syndrome, sarcopenia

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥ 45 years
  • Respiratory insufficiency requiring mechanical ventilation (MV)
  • ICU presentation < 6 days
  • Patient or legally authorized representative able to provide written or witnessed verbal informed consent in English
  • All four limbs intact and mobile
  • Eligible for and able to participate in physical therapy
  • Pre admission Barthel Index >70

Exclusion Criteria:

  • Acute kidney injury with a glomerular filtration rate < 30 ml/min
  • Diagnosis of severe organ dysfunction including end stage liver disease or cirrhosis
  • Diagnosis of active cancer
  • Acute or chronic organ transplant rejection
  • Exceedingly high mechanical ventilator settings (FiO2>60%, PEEP>12) or alternative modes of mechanical ventilation (inverse ratio pressure control, airway pressure release ventilation)
  • Severe functional impairment or physical impairment to rehabilitation
  • On high dose vasopressor agents (> 5mcg of norepinephrine or equivalent)
  • Liver function tests > 2.5 x normal limits (normal reference ranges include AST between 10 and 40 units/L or ALT between 7 and 56 units/L)
  • Chronic dementia or cognitive impairment

Sites / Locations

  • U of Maryland, Baltimore, Professional Schools IRB

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Mobility-based Physical Rehab (MPR)

MPR and Neuromuscular Stimulation and HPRO

Arm Description

ICU control group receiving only mobility based rehabilitation (MPR).

ICU group receiving mobility based rehabilitation and NMES and High protein supplementation.

Outcomes

Primary Outcome Measures

Muscle mass
Muscle mass as measured by lower extremity muscle volume
Global body strength
Muscle group strength as measured by hand held dynamometer and by hand grip strength
Mobility status
Outcome as measured by combined 6 minute walk distance and gait speed
Short Physical Performance Battery
Short Physical Performance battery will be assessed at baseline and at 7 and 14 days.

Secondary Outcome Measures

Time to weaning
As measured by ventilator days
ICU/Hospital length of stay
Days in the ICU, days in the hospital
Discharge disposition
home, nursing home, acute rehabilitation, readmission, death, remains hospitalized
Weaning success
proportion of patient successfully weaned with in a 14 day period, and eventually

Full Information

First Posted
July 21, 2015
Last Updated
February 9, 2023
Sponsor
University of Maryland, Baltimore
search

1. Study Identification

Unique Protocol Identification Number
NCT02509520
Brief Title
Assessing The Effects of Exercise, Protein, and Electric Stimulation On Intensive Care Unit Patients Outcomes
Acronym
ExPrEs
Official Title
Rehabilitation, NMES and High Protein to Reduce Post ICU Syndrome in the Elderly
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
May 1, 2015 (undefined)
Primary Completion Date
December 1, 2023 (Anticipated)
Study Completion Date
January 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Maryland, Baltimore

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Elderly patients who experience a prolonged ICU stay are at high risk for developing post intensive care unit syndrome (PICS), a serious medical condition manifested by loss of muscle mass, weakness, malnutrition and neurocognitive decline. PICS often leads to chronic disability, prolonged mechanical ventilation and the need for costly extended stays in long term care facilities (LTCs). The investigators' preliminary study shows attempts at rehabilitating patients who have already developed PICS are minimally effective, resulting in only modest improvements in functionality. This project will determine the effects of mobility-based physical rehabilitation (MPR) combined with neuromuscular electric stimulation (NMES) and high protein supplementation (HPRO) early in a patients ICU stay on preventing PICS related musculoskeletal and functional deficits, and improving clinical outcomes.
Detailed Description
Older, critically ill patients who survive their ICU stay frequently develop post-ICU syndrome (PICS) - a condition manifested by sarcopenia, weakness, malnutrition and neurocognitive decline - which occurs as a result of a critical illness, prolonged bed rest, catabolism, and polypharmacy. PICS frequently leads to chronic disability, prolonged mechanical ventilation (MV), functional deficits, and the need for extended rehabilitation in long term care facilities (LTCs). As the majority of patients admitted to ICUs are ≥ 65 years old, many of these patients are at high risk for PICS. Since the care of ICU patients is primarily focused on the medical management of the acute critical illness, there are limited resources and strategies available to prevent PICS. Evidence suggests mobility-based physical rehabilitation (MPR) combined with resistive training with neuromuscular electric stimulation (NMES) and high protein diets (HPRO) containing essential amino acids can mitigate the loss of muscle mass and function during bed rest in the elderly. The investigators hypothesize that preventive therapy involving the addition of both NMES and HPRO to MPR early and throughout the ICU and hospital stay can mitigate PICS-associated sarcopenia, malnutrition, and immobility to confer valuable health benefits toward recovery. To test this, the investigators will use a 2x2 factorial design in which older, MV ICU patients will all receive comprehensive ICU care and MPR, then be randomized to one of 4 groups: 1) MPR+NMES, 2) MPR+HPRO, 3) all 3 together, or 4) MPR alone (control), to determine independent and combined effects of the interventions. The Specific Aims are to 1) determine the effects of adding NMES and HPRO interventions to MPR on muscle mass, strength, and mobility function in older, critically ill MV patients while still in the ICU, and 2) determine the effects of adding NMES and HPRO interventions to MPR on the clinical outcomes of time to weaning from MV, ICU/hospital length of stay and discharge disposition of these patients. This proposal capitalizes on the interdisciplinary collaboration among Pulmonary/Critical Care Intensivists, Physical Therapists, Geriatricians, Clinical Nutritionists, Statisticians and Nutrition and Metabolism clinical researchers examining the efficacy of the proposed comprehensive rehabilitation approach. The investigators' primary goal is to attenuate the severity of sarcopenia and functional decline in this older, critically ill population at risk for severe disability. Additionally, by focusing on maintaining skeletal muscle mass, function, and strength, the investigators hope to improve clinical outcomes. The investigators posit this combined therapy will mitigate PICS-associated disability and speed the recovery from critical illness in older, MV ICU patients. This project has high overall impact as the intervention is easily administered by hospital staff and may greatly reduce the physiological and functional declines while hastening recovery during acute ICU hospitalization in older adults.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Muscle Weakness, Critical Illness, Sarcopenia
Keywords
Nutritional supplementation, Neuromuscular Electric Stimulation, ICU acquired weakness, Post ICU Syndrome, sarcopenia

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Mobility-based Physical Rehab (MPR)
Arm Type
No Intervention
Arm Description
ICU control group receiving only mobility based rehabilitation (MPR).
Arm Title
MPR and Neuromuscular Stimulation and HPRO
Arm Type
Active Comparator
Arm Description
ICU group receiving mobility based rehabilitation and NMES and High protein supplementation.
Intervention Type
Dietary Supplement
Intervention Name(s)
MPR and High Protein Supplement (HPRO) and Neuromuscular Electric Stimulation (NMES)
Intervention Description
The MPR provides strength and cardiopulmonary endurance training, which consist of exercises to promote function movements. Intensity is based on patient's hemodynamic responses and subjective report using Modified Borg Dyspnea Scale. Intensity, duration, or type of activity will be modified each session to achieve a moderately intense physiologic response. The NMES protocol requires self-adhesive surface electrodes be placed on quadriceps muscles and lower leg bilaterally, twice daily. This protocol is based on prior NMES protocols used to stimulate muscle protein synthesis in older diabetic patients, preserve muscle mass in intensive care patients and increase strength in older adults after knee replacement. The HPRO intervention is based on caloric needs, calculated using validated equations to maintain positive nitrogen balance. Protein will be supplemented as isolated amino acids twice/day to deliver ~15g of essential amino acids per serving, with a goal of 1.6 g/kg/day.
Primary Outcome Measure Information:
Title
Muscle mass
Description
Muscle mass as measured by lower extremity muscle volume
Time Frame
14 days
Title
Global body strength
Description
Muscle group strength as measured by hand held dynamometer and by hand grip strength
Time Frame
14 days
Title
Mobility status
Description
Outcome as measured by combined 6 minute walk distance and gait speed
Time Frame
14 days
Title
Short Physical Performance Battery
Description
Short Physical Performance battery will be assessed at baseline and at 7 and 14 days.
Time Frame
14 days
Secondary Outcome Measure Information:
Title
Time to weaning
Description
As measured by ventilator days
Time Frame
14 days
Title
ICU/Hospital length of stay
Description
Days in the ICU, days in the hospital
Time Frame
14 days
Title
Discharge disposition
Description
home, nursing home, acute rehabilitation, readmission, death, remains hospitalized
Time Frame
30 days
Title
Weaning success
Description
proportion of patient successfully weaned with in a 14 day period, and eventually
Time Frame
14 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 45 years Respiratory insufficiency requiring mechanical ventilation (MV) ICU presentation < 6 days Patient or legally authorized representative able to provide written or witnessed verbal informed consent in English All four limbs intact and mobile Eligible for and able to participate in physical therapy Pre admission Barthel Index >70 Exclusion Criteria: Acute kidney injury with a glomerular filtration rate < 30 ml/min Diagnosis of severe organ dysfunction including end stage liver disease or cirrhosis Diagnosis of active cancer Acute or chronic organ transplant rejection Exceedingly high mechanical ventilator settings (FiO2>60%, PEEP>12) or alternative modes of mechanical ventilation (inverse ratio pressure control, airway pressure release ventilation) Severe functional impairment or physical impairment to rehabilitation On high dose vasopressor agents (> 5mcg of norepinephrine or equivalent) Liver function tests > 2.5 x normal limits (normal reference ranges include AST between 10 and 40 units/L or ALT between 7 and 56 units/L) Chronic dementia or cognitive impairment
Facility Information:
Facility Name
U of Maryland, Baltimore, Professional Schools IRB
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Assessing The Effects of Exercise, Protein, and Electric Stimulation On Intensive Care Unit Patients Outcomes

We'll reach out to this number within 24 hrs