- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04938531
Targeted Exercise Intervention to Reduce Morbidity and Mortality in Sepsis (TERMS)
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.
Study Overview
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.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ontario
-
London, Ontario, Canada, N6A 5W9
- London Health Sciences Centre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Exercise
Exercise, passive
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The proportion of prescribed exercise sessions completed by each participant
Time Frame: 28 days
|
proportion of prescribed exercise sessions completed by each participant
|
28 days
|
The proportion of successfully completed measurements for each patient.
Time Frame: 28 days
|
Proportion of measurements completed
|
28 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Inflammatory mediator levels
Time Frame: 28 days
|
Biomarker (TNF, IL-1) levels at end of exercise
|
28 days
|
MCAv
Time Frame: 60 minutes
|
Middle Cerebral Artery blood flow velocity (measured by Doppler) during exercise
|
60 minutes
|
Cardiac function
Time Frame: 60 minutes
|
Global Longitudinal Strain measured by echocardiography during exercise
|
60 minutes
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Ian Ball, MD, FRCPC, London Health Sciences Centre
Publications and helpful links
General Publications
- 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.
- Adler J, Malone D. Early mobilization in the intensive care unit: a systematic review. Cardiopulm Phys Ther J. 2012 Mar;23(1):5-13.
- 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.
- 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.
- 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.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 105319
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Severe Sepsis
-
Indonesia UniversityCompletedSevere Sepsis With Septic Shock | Severe Sepsis Without Septic ShockIndonesia
-
Beckman Coulter, Inc.Biomedical Advanced Research and Development AuthorityRecruitingSevere Sepsis | Severe Sepsis Without Septic ShockUnited States
-
Rennes University HospitalUnknownSevere Sepsis or Septic Shock
-
Beckman Coulter, Inc.CompletedSepsis | Severe Sepsis | Severe InfectionFrance, Spain
-
Yonsei UniversityCompletedSevere Sepsis or Septic ShockKorea, Republic of
-
University of RostockCompletedSevere Sepsis and Septic ShockGermany
-
Centre Hospitalier Universitaire de NiceUnknownComparison of Sensitivity Between Presepsine and Lactate for the Diagnosis of Severe Sepsis. (PREDI)Severe Sepsis and Septic ShockFrance
-
University Hospital, Strasbourg, FranceUnknownSevere Sepsis and Septic ShockFrance
-
Peking Union Medical College HospitalUnknownLactate | Severe Sepsis With Septic Shock
-
University of UtahNational Institutes of Health (NIH)CompletedSevere Sepsis With Septic Shock
Clinical Trials on Exercise
-
University of Kansas Medical CenterRecruiting
-
National Institute of Neurological Disorders and...TerminatedTraumatic Brain InjuryUnited States
-
Toronto Rehabilitation InstituteCompletedAcute Myeloid LeukemiaCanada
-
University of Texas, El PasoRecruitingKnee Osteoarthritis | Knee Pain Chronic | Central Pain SyndromeUnited States
-
Sahmyook UniversityRecruitingChronic Nonspecific Neck PainKorea, Republic of
-
University of AlbertaWomen and Children's Health Research Institute, CanadaRecruitingType 1 Diabetes | Post-menopauseCanada
-
Uskudar UniversityCompleted
-
Yuksek Ihtisas UniversityCompletedDementia | Frailty | Cognitive Function | Reaction Time | Aerobic Exercise | Balance ExerciseTurkey
-
National Taiwan Normal UniversityCompletedAging | Cognitive DeclineTaiwan
-
Wayne State UniversityUnknown