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Bed Rest and Muscle Strength in ICU: Interest in the Early Association of NEMS With Cyclo-ergometer Mobilization

Bed Rest and Muscle Strength in Resuscitation Patients: Interest in the Early Association of NEMS With Cyclo-ergometer Mobilization

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03987997
Acronym
AFMPR
Enrollment
55
Registered
2019-06-17
Start date
2018-08-09
Completion date
2021-12-26
Last updated
2019-06-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Weakness, Muscle

Keywords

Intensive Care Units, Critical Illness, Rehabilitation, Muscle atrophy, Muscle weakness, Cyclo-ergometer, Electrical muscle stimulation

Brief summary

Muscles atrophy and weakness are common in intensive care units, their origin is multifactorial. Passive then active mobilization with cyclo-ergometer have shown to improve functional abilities and limit muscle weakness among intensive care unit patients. Electrical muscle stimulation should limit the atrophy and muscle weakness in intensive care unit associated with early mobilization. This study aims to compare the association early cyclo-ergometer mobilization with electrical muscle stimulation versus cyclo-ergometer mobilization only to prevent muscle atrophy and weakness in intensive care unit.

Interventions

DEVICEEarly association of electrical muscle stimulation with cyclo-ergometer

Early electrical muscle stimulation in patients usually mobilized with cyclo-ergometer in ICU.

Sponsors

Direction Centrale du Service de Santé des Armées
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

Only one leg receives the electrical muscle stimulation, the leg which receives the electrical stimulation is randomized. An outcome assessor assess the outcome blindly.

Intervention model description

Leg with electrical muscle stimulation and cycling versus leg with cycling only

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patient affiliated to a social security scheme * Patient hospitalized in intensive care unit for medical or surgical reasons, under assisted ventilation (invasive, non-invasive ventilation or oxygen-therapy at high speed via the Optiflow(r) system delivering a flow between 30 and 60 L.min and a FiO2 between 30 and 100%) * State of the patient deemed stable buy the doctor responsible for the care and allowing the action of the physiotherapist (acts on medical prescription) * Age more than 18 years old (major patient) and less than 75 years old * Duration of mechanical ventilation (invasive or not) less than or equal to 72 hours at the beginning of the inclusion * Predicable duration of stay greater than or equal to 3 days

Exclusion criteria

* Impossibility to know the consent of the patient, his legal representative or the person of trust * Patient under safeguard of justice, tutorship or curatorship * Legionnaire not rectified * Cardiac stimulator or defibrillator * Cardiorespiratory state clinically not compatible withe early mobilization * Neurological problems: intracranial pressure \> 20 mmHg, presence of ICU acquired neuropathy, pre-existing diagnosis of neuromuscular disease (MS, ALS...), acute stroke, epilepsy * Orthopedic problems: even partial amputation of a lower limb, unstable fracture, suspicion of fracture, non-fixed spinal cord injury, use of a technique that does not allow to comply with postoperative surgical instructions (range of motion, discharge...), untreated deep vein thrombosis, traumatic sequelae to the origin of disabling manifest muscle weakness of a lower limb at admission * Dermatological problems: severe lesions or complex dressing in the lower limbs * Morphological criteria : size \< 1.5m, BMI \> 35 * Confirmed psychiatric illness or severe agitation * Abdominal surgery without protection by compression belt (medical prescription), or too fragile (medical opinion) * Pregnant or lactating women (postpartum is not an exclusion criterion) * Patients over 75 years old * Hemiplegia / sequential hemiparesis * Impossibility to practice electrostimulation on at least one lower limb (manifest muscle weakness of a lower limb at admission (e. g. related to a traumatic sequelae)

Design outcomes

Primary

MeasureTime frameDescription
Change of muscle mass of quadriceps assessed with ultrasonographyat day 0, then every 7 days (+/- 2 days) until ICU discharge (at least 6 months)Muscle mass of quadriceps assessed by ultrasonography. The member who receives the cyclo-ergometer mobilization alone serves as a control for the member who receives the mobilization by cyclo-ergometer and electrical muscle stimulation

Secondary

MeasureTime frameDescription
Change of muscle strength of lower limb assessed by dynamometryat day 0, then every 7 days (+/- 2 days) until ICU discharge (at least 6 months)Muscle strength of lower limb assessed by dynamometry. The member who receives the cyclo-ergometer mobilization alone serves as a control for the member who receives the mobilization by cyclo-ergometer and electrical muscle stimulation
Change of pedalling symmetry right/leftat day 0, then every 7 days (+/- 2 days) until ICU discharge (at least 6 months)Assessed with the cyclo-ergometer associated pic torque
Change of power variation of lower limbat day 0, then every 7 days (+/- 2 days) until ICU discharge (at least 6 months)Power variation of lower limb assessed with cyclo-ergometer
Change of work variation of lower limbEvery cyclo-ergometer session, 5 days on 7 (at least 6 months)Work variation of lower limb assessed with cyclo-ergometer

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026