EARTH-ICU: Early Physical Therapy in Patients With Sepsis

Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain (Other)
Overall Status
Terminated
CT.gov ID
NCT01787045
Collaborator
(none)
29
1
2
33
0.9

Study Details

Study Description

Brief Summary

It is clearly shown that patients in the Intensive care Unit (ICU) with severe sepsis or multi organic failure are very susceptible to develop neuromuscular complications. That can be attributed to a hyper catabolic state, general inflammation and immobilization. This can leads a significant muscle wasting, polyneuropathy and/or myopathy. These alterations have been defined with the term Intensive Care Acquired Weakness (ICUAW) and can leads important functional squeals and impaired quality of life for months, years and in some cases irreversibly.

To overcome these complications, early activation by physiotherapy becomes an important tool. This type of treatment has been show to be feasible, safe and improves the functional capacity of patients. In addition to a reduction in the duration of ICU and hospital stay and improved quality of life for patients.

The objective of this study is to demonstrate that the early and active physical activity in patients with severe sepsis can limit the loss of muscle mass and complications related to this type of damage.

Procedures: Patients or relatives will be asked to participate in the study. If a positive response is done, patients will be randomized in an intervention or control group.

A baseline evaluation will be performed during the first day of study admission. That includes a physical exploration, electrophysiological studies, skeletal muscle histological/biochemical evaluations and monitoring of blood biomarkers and others clinical outcomes will be registered.

Intervention will be divided in a morning and afternoon times, patient will be positioned in chair or bed and mobilized by physiotherapist. As usual, all patients will be attaining manual mobilization for 20 minutes twice a day. Only for intervention group, additional cycle-ergometer exercise will be performed for 30 minutes at better performance achieved and tolerated for patient. All vitals parameters will be strictly controlled before, during and after intervention.

The same baseline evaluation will be repeated after day 7 and clinical outcomes will be registered until ICU discharge.

Condition or Disease Intervention/Treatment Phase
  • Other: Early and Active Physical Therapy
  • Other: Passive Range of Motion
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
29 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Basic Science
Official Title:
Effect of Early Physical Activity on Skeletal Muscle Signaling Pathways Controlling Protein Turnover in Patients With Sepsis.
Study Start Date :
Feb 1, 2013
Actual Primary Completion Date :
Jun 1, 2015
Actual Study Completion Date :
Nov 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Group

Early and Active Physical Therapy will be performed by physiotherapist twice a day. During first week patients will be positioned in chair or bed and performed cycle-ergometer exercise during 30 min. Our physiotherapy protocol will be continued until Intensive Care Unit (ICU) discharge.

Other: Early and Active Physical Therapy
Cycle-ergometer exercise will be performed in the more active manner tolerated by patient. Potency attained will be registered during 30 min of exercise. Our physiotherapy protocol includes also others exercises like ambulation with assistance, cycle-ergometer for arms and legs, etc.
Other Names:
  • Early Physical Rehabilitation
  • Early Physical Training
  • Early Physiotherapy
  • Early Mobilization
  • Very Early Mobilisation
  • Early Exercise
  • Early Activity
  • Early Mobility Therapy
  • Other: Passive Range of Motion
    Passive mobilization will be performed in all limbs as 10 repetitions of every range of motions. Extension position will be maintained for some seconds to attaint muscular elongation in every muscular group.
    Other Names:
  • Passive Range of Motion (PROM)
  • Passive Mobilization
  • Articular mobilization
  • Routinary Passive Range of Motion
  • Usual manual mobilization
  • Other: Control Group

    Routinary Passive Range of Motion will be performed by physiotherapist 20 min and twice a day until ICU discharge.

    Other: Passive Range of Motion
    Passive mobilization will be performed in all limbs as 10 repetitions of every range of motions. Extension position will be maintained for some seconds to attaint muscular elongation in every muscular group.
    Other Names:
  • Passive Range of Motion (PROM)
  • Passive Mobilization
  • Articular mobilization
  • Routinary Passive Range of Motion
  • Usual manual mobilization
  • Outcome Measures

    Primary Outcome Measures

    1. Change in activation of skeletal muscle synthetic and catabolic pathways. [Within the first 7 days (plus or minus 1 days)]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 85 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Hemodynamically stable patients.

    • Admitted to ICU for sepsis or MOF (multiple organ failure) or who developing during their ICU stay within the first 24 hours of the ICU admission.

    • With an expected ICU stay of at least 7 days.

    Exclusion Criteria:
    • Patients without approved consent.

    • Patients with a known neuromuscular disorder before ICU admission.

    • Moribund patients.

    • Severe metabolic/hemodynamic instability despite pharmacological support.

    • Having conditions that impair evaluation techniques or intervention methods.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Cliniques universitaires Saint-Luc- Université Catholique de Louvain (StLuc) Brussels Belgium 1200

    Sponsors and Collaborators

    • Cliniques universitaires Saint-Luc- Université Catholique de Louvain

    Investigators

    • Study Chair: Pierre-François Laterre, Professor, Cliniques universitaires Saint-Luc- Université Catholique de Louvain (StLuc)

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Cliniques universitaires Saint-Luc- Université Catholique de Louvain
    ClinicalTrials.gov Identifier:
    NCT01787045
    Other Study ID Numbers:
    • EarlyPTProtocol1
    First Posted:
    Feb 8, 2013
    Last Update Posted:
    Nov 17, 2015
    Last Verified:
    Nov 1, 2015
    Keywords provided by Cliniques universitaires Saint-Luc- Université Catholique de Louvain
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 17, 2015