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Haemodynamic and Metabolism Response During Early Rehabilitation in Sedated Patients

NCT02920684 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2017-08-02

No results posted yet for this study

Summary

Despite several positive studies, benefits of early rehabilitation on recovery and motor performance improvement need to be demonstrate. A recent study finds that despite early rehabilitation, 1 survivor of 2 (52%) acquired an ICU weakness. The low intensity exercises applied in intensive care is common and most patients stay in bed.

Under these conditions, the optimal choice of the rehabilitation technique for bedridden patient and its intensity should be studied.

The objective of the study is to evaluate the cardiovascular and metabolic response of patients during four interventions: Passive legs mobilization, Passive cycloergometter, Quadriceps neuromuscular electrical stimulation and Functional electrical stimulation.

Conditions

  • Critically Ill Patients Under Mechanical Ventilation
  • Sedated Patients

Interventions

OTHER

Passive legs mobilisation

A physiotherapist performs a passive leg movement

OTHER

Passive cycloergometer

A motorised cycloergometer performs a passive cycling

OTHER

Muscular electrical stimulation

A neuromuscular electrical stimulation device performs a quadriceps located stimulation

OTHER

FES cycling

A motorised cycloergometer performs a passive cycling with quadriceps neuromuscular stimulation

Sponsors & Collaborators

  • University Hospital, Rouen

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-12-31
Primary Completion
2017-08-31
Completion
2017-08-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02920684 on ClinicalTrials.gov