Locomotor Muscle Oxygenation and Activation During Acute Interval Compared to Constant-load Bed-cycling Exercise
Intensive Care Unit Acquired Weakness, Critical Illness
About this trial
This is an interventional treatment trial for Intensive Care Unit Acquired Weakness focused on measuring ICU acquired muscle weakness, Quadriceps muscle, Near-infrared spectroscopy, Oxygenation, EMG, Early-mobilization, Bed-cycling, Interval exercise, Continuous exercise
Eligibility Criteria
Inclusion Criteria:
- Full cooperatively adult patients indicated by the Adequacy Score of standardized 5 questions (SQ5) = 5/5
- Patients mechanically ventilated for longer than 48 hours during the same ICU admission
- Patients are expected to remain in the ICU for more than an additional 48 hours starting from study enrollment
- Patients able to perform active cycling for > 10 consecutive minutes
Exclusion Criteria:
- Pre-existing functional limitations
- Low limb injuries or conditions that would preclude in-bed cycling such as a body habitus unable to fit the bike
- Extreme obesity (body mass index >35 kg/m2)
- Neurologically unstable
- Acute surgery
- Palliative goals of care
- Temperature > 40 °C
- An anticipated fatal outcome
- Evidence of coronary ischaemia, for example, chest pain or electrocardiogram changes
- Resting heart rate <40 or >120 beats per minute
- Mean arterial pressure <60 or >120 mmHg
- Peripheral capillary oxygen saturation < 90%
- Wounds, trauma or surgery of leg precluding cycle ergometry
- Wounds, trauma or surgery of pelvis precluding cycle ergometry
- Wounds, trauma or surgery of lumbar spine precluding cycle ergometry
- Coagulation disorder (international normalised ratio > 1.8, or platelets < 50,000 mcL)
- Intracranial pressure >20 mm Hg
- Femoral access other than femoral central line
- Acute deep vein thrombosis
- Pulmonary embolism
- >20 mcg/min of noradrenaline
- inotropic or vasopressor support comparable to a dose of noradrenaline >20mcg/min
- Fraction of inspired oxygen > 55%
- Arterial partial pressure of oxygen (PaO2) <65 torr (<8.66 kPa)
- Positive end-expiratory pressure > 10 cmH2O
- Respiratory rate > 30 breaths per minutes with adequate ventilatory support
- Minute ventilation >150 mL/kg body weight
Sites / Locations
- University Hospital LeuvenRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Arm 1 (First constant-load then interval bed-cycling protocol)
Arm 2 (First interval then constant-load bed-cycling protocol)
During Day 1, patients will be familiarized with the constant-load and interval bed-cycling exercise against no resistance. Patients will be also randomized in the two arms of the study before the determination of the appropriate exercise intensities to be subsequently use during the constant-load and interval bed-cycling protocols on Day 2 and Day 3. Exercise intensities will be determined so that the volume of training during the two protocols will be equal. During Day 2, patients randomized to arm 1 will perform the constant-load bed-cycling protocol. During Day 3, patients who executed the constant-load bed-cycling protocol on Day 1 (arm 1) will perform the interval bed-cycling protocol.
During Day 1, patients will be familiarized with the constant-load and interval bed-cycling exercise against no resistance. Patients will be also randomized in the two arms of the study before the determination of the appropriate exercise intensities to be subsequently use during the constant-load and interval bed-cycling protocols on Day 2 and Day 3. Exercise intensities will be determined so that the volume of training during the two protocols will be equal. During Day 2, patients randomized to arm 2 will perform the interval bed-cycling protocol. On Day 3 they will perform the constant-load bed-cycling protocol.