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Targeted Exercise Intervention to Reduce Morbidity and Mortality in Sepsis (TERMS)

Primary Purpose

Severe Sepsis

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Exercise
Sponsored by
Lawson Health Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Severe Sepsis focused on measuring Sepsis, Exercise, Intervention

Eligibility Criteria

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

Inclusion Criteria:

  • Severe sepsis defined as:

    1. 2 of 4 Systemic Inflammatory Response Syndrome criteria,
    2. a confirmed or clinically suspected source of infection and,
    3. two or more organ dysfunction (using standard definitions).

Exclusion Criteria:

  • Greater than 48h since severe sepsis criteria were met
  • inability to perform passive exercise using bedside leg cycle,
  • limitations on life support interventions (No CPR or No defibrillation by themselves are not an exclusion),
  • major limitation in neurologic or physical function prior to onset of severe sepsis (e.g. wheelchair or nursing home dependent),
  • patients receiving neuromuscular blocking drugs or sedation targeted to a MAAS score less than 3,
  • allergies to sulfonamide drugs or iodides due to possibility of an allergic reaction to ICG.

Sites / Locations

  • London Health Sciences Centre

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Exercise

Arm Description

Exercise, passive

Outcomes

Primary Outcome Measures

The proportion of prescribed exercise sessions completed by each participant
proportion of prescribed exercise sessions completed by each participant
The proportion of successfully completed measurements for each patient.
Proportion of measurements completed

Secondary Outcome Measures

Inflammatory mediator levels
Biomarker (TNF, IL-1) levels at end of exercise
MCAv
Middle Cerebral Artery blood flow velocity (measured by Doppler) during exercise
Cardiac function
Global Longitudinal Strain measured by echocardiography during exercise

Full Information

First Posted
August 24, 2017
Last Updated
June 16, 2021
Sponsor
Lawson Health Research Institute
Collaborators
Schulich School of Medicine and Dentistry
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1. Study Identification

Unique Protocol Identification Number
NCT04938531
Brief Title
Targeted Exercise Intervention to Reduce Morbidity and Mortality in Sepsis
Acronym
TERMS
Official Title
Targeted Exercise Intervention to Reduce Morbidity and Mortality in Sepsis
Study Type
Interventional

2. Study Status

Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
February 25, 2015 (Actual)
Primary Completion Date
May 31, 2019 (Actual)
Study Completion Date
May 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lawson Health Research Institute
Collaborators
Schulich School of Medicine and Dentistry

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a single arm, pilot study. Patients in the LHSC adult ICU (Critical Care Trauma Centre) (1200 patients/annum) are screened daily for severe sepsis by the Clinical Research Assistants. Severe sepsis is defined as infection, systemic inflammation and sepsis-induced dysfunction of at least one organ system. Study consent is obtained from the patient or substitute decision maker. Our objective in this pilot study is to determine the feasibility of delivering a regular passive exercise intervention, and collecting relevant outcome data early in the course of severe sepsis in critically ill patients. We hypothesize that early passive exercise in septic patients will reduce inflammation, endothelial cell injury, microvascular hypoperfusion and mortality. Our goal is to provide the evidence from comprehensive analysis of biochemical, physiologic and patient outcomes to develop a definitive multi-centre clinical trial.
Detailed Description
Participants will perform an entry passive exercise test within 48 hours of onset of severe sepsis. Patients then will perform 30-60 min supine passive cycle ergometry exercise 5 days/week. Details of frequency and duration of each training session will be recorded along with measures of heart rate, hemoglobin oxygen saturation and blood pressure. The exercise tests will consist of baseline, 30 minutes of supine passive leg cycle ergometry, and a subsequent 60 minute recovery period. Arterial and venous blood samples obtained during the three protocol phases will be analyzed for metabolic factors (blood gases, oxygen content, pH, lactate, glucose). On day 0, 1, and 7, an additional blood tube is immediately transferred on ice to the Translational Research Centre Biohazard Level 2 Laboratory for processing and aliquoting using a standard operating procedure. Plasma will be stored at -80C and thawed immediately before use in biochemical analyses or in vitro experiments. Analysis will include inflammatory mediator levels, blood vessel permeability in leg muscle and leg muscle perfusion as described below. Additional measures of central and peripheral hemodynamics will include ultrasound-based measures of cardiac stroke volume, carotid blood flow, and carotid artery compliance. Continuous analog measures of the electrocardiogram, central venous pressure, blood pressure, end tidal carbon dioxide and electromyography (quadriceps) will be monitored during the exercise and stored online for subsequent analysis of heart and respiratory rate variability, blood pressure variability and baroreflex sensitivity. We will also record length of ICU stay, in-hospital mortality and hospital health care costs. Length of ICU and hospital stay will be used as surrogates for hospital costs. Physiotherapy time will also be recorded for each patient (time on the intervention and total time with each enrolled patient). Energy requirements will be assessed by metabolic measurements; nitrogen balance and serum prealbumin will be measured to monitor nutritional status. The mechanistic basis of the observed hemodynamics during and following passive leg exercise will be explored using a comprehensive translational model that incorporates 1) venous blood analysis, 2) in vitro human-derived cell culture models, and 3) in vivo skeletal muscle measures of capillary blood flow. This panel will be evaluated on day 0, 7 and 28. Venous Blood Analysis: Patient inflammatory profiles will be determined by assaying stored plasma samples for inflammatory biomarkers and inflammatory-inducing actions. We will measure a previously established list of 20+ inflammatory biomarkers elevated in sepsis, including cytokines, chemokines, matrix metalloproteinases, collagen breakdown products, neurotrophins and stress hormones (cortisol). The innate immune response will also be evaluated. HIF1alpha, a subunit of the transcription factor HIF1, is a key regulator of the innate immune response to inflammation. Exercise results in increased free DNA in the plasma which leads to induced HIF1alpha expression. Thus, HIF1alpha is a potential candidate to orchestrate gene expression changes that initiate adaptations of the innate immune response after exercise. HIF-1alpha, downstream target genes and plasma free DNA levels in blood samples will be measured to determine the effects of exercise on the innate immune response during sepsis. In vitro cell culture: Human plasma will be applied to human-derived endothelial cells representing various vascular beds (e.g. cerebral and dermal microvasculature, and large blood vessels such as aorta and veins) to assess inflammatory potential: measurable targets include reactive oxygen species, nitric oxide, NF-kB, MAP kinases, leukocyte adhesion assays, and permeability. Plasma will also be applied to erythrocytes to determine inflammatory-induced changes in morphology, an assay critical to understanding oxygen carrying capacity. In vivo capillary blood flow: The occurrence of muscle hypoperfusion and increased vascular permeability will be assessed using an in-house-developed near-infrared spectroscopy (NIRS) method that monitors the uptake of a light-absorbing dye in the muscle. The dye, indocyanine green (ICG), has been used clinically for over 30 years and has a high safety record. Muscle perfusion and vascular permeability are determined by using a mathematical model to characterize the dynamics of the ICG distribution in muscle following an intravenous injection. This approach is analogous to contrast-enhanced imaging methods (CT and MRI), but with the advantage that the portability of NIRS enables bedside measurements.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Sepsis
Keywords
Sepsis, Exercise, Intervention

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise
Arm Type
Experimental
Arm Description
Exercise, passive
Intervention Type
Other
Intervention Name(s)
Exercise
Intervention Description
Participants will perform an entry passive exercise test within 48 hours of onset of severe sepsis. Patients then will perform 30-60 min supine passive cycle ergometry exercise 5 days/week.
Primary Outcome Measure Information:
Title
The proportion of prescribed exercise sessions completed by each participant
Description
proportion of prescribed exercise sessions completed by each participant
Time Frame
28 days
Title
The proportion of successfully completed measurements for each patient.
Description
Proportion of measurements completed
Time Frame
28 days
Secondary Outcome Measure Information:
Title
Inflammatory mediator levels
Description
Biomarker (TNF, IL-1) levels at end of exercise
Time Frame
28 days
Title
MCAv
Description
Middle Cerebral Artery blood flow velocity (measured by Doppler) during exercise
Time Frame
60 minutes
Title
Cardiac function
Description
Global Longitudinal Strain measured by echocardiography during exercise
Time Frame
60 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Severe sepsis defined as: 2 of 4 Systemic Inflammatory Response Syndrome criteria, a confirmed or clinically suspected source of infection and, two or more organ dysfunction (using standard definitions). Exclusion Criteria: Greater than 48h since severe sepsis criteria were met inability to perform passive exercise using bedside leg cycle, limitations on life support interventions (No CPR or No defibrillation by themselves are not an exclusion), major limitation in neurologic or physical function prior to onset of severe sepsis (e.g. wheelchair or nursing home dependent), patients receiving neuromuscular blocking drugs or sedation targeted to a MAAS score less than 3, allergies to sulfonamide drugs or iodides due to possibility of an allergic reaction to ICG.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ian Ball, MD, FRCPC
Organizational Affiliation
London Health Sciences Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
London Health Sciences Centre
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5W9
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
23984731
Citation
Angus DC, van der Poll T. Severe sepsis and septic shock. N Engl J Med. 2013 Aug 29;369(9):840-51. doi: 10.1056/NEJMra1208623. No abstract available. Erratum In: N Engl J Med. 2013 Nov 21;369(21):2069.
Results Reference
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PubMed Identifier
23883525
Citation
Denehy L, Skinner EH, Edbrooke L, Haines K, Warrillow S, Hawthorne G, Gough K, Hoorn SV, Morris ME, Berney S. Exercise rehabilitation for patients with critical illness: a randomized controlled trial with 12 months of follow-up. Crit Care. 2013 Jul 24;17(4):R156. doi: 10.1186/cc12835.
Results Reference
background
PubMed Identifier
22807649
Citation
Adler J, Malone D. Early mobilization in the intensive care unit: a systematic review. Cardiopulm Phys Ther J. 2012 Mar;23(1):5-13.
Results Reference
background
PubMed Identifier
24436844
Citation
Parker A, Sricharoenchai T, Needham DM. Early Rehabilitation in the Intensive Care Unit: Preventing Physical and Mental Health Impairments. Curr Phys Med Rehabil Rep. 2013 Dec;1(4):307-314. doi: 10.1007/s40141-013-0027-9.
Results Reference
background
PubMed Identifier
24508202
Citation
Sricharoenchai T, Parker AM, Zanni JM, Nelliot A, Dinglas VD, Needham DM. Safety of physical therapy interventions in critically ill patients: a single-center prospective evaluation of 1110 intensive care unit admissions. J Crit Care. 2014 Jun;29(3):395-400. doi: 10.1016/j.jcrc.2013.12.012. Epub 2013 Dec 30.
Results Reference
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Targeted Exercise Intervention to Reduce Morbidity and Mortality in Sepsis

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