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Study on the application of mobilization in the first 48 hours of hospitalization in comparison to the mobilization associated with muscle stimulation with electrical impulses in patients hospitalized in the ICU

Randomized trial about the application of an early mobilization protocol in comparison with early mobilization associated with neuromuscular electrical stimulation in critically ill patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3w3kmg
Enrollment
Unknown
Registered
2019-04-08
Start date
2018-05-07
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Disuse hipotrophy

Interventions

- Early Mobilization Participants: 21 Intervention: daily, from the time of randomization to discharge from the ICU. Protocol: It consists of 6 phases according to the level of consciousness and motor
Other
Z50.1
E02.331

Sponsors

Universidade de São Paulo
Lead Sponsor
Faculdade de Medicina de Ribeirão Preto
Collaborator

Eligibility

Age
18 Years to 120 Years

Inclusion criteria

Inclusion criteria: Patients admitted to the ICU for less than 48 hours; older than 18 years; both sexes; signature of the Free and Informed Consent Form is mandatory; exclusion criteria

Exclusion criteria

Exclusion criteria: Inability to walk without assistance before the acute illness that led to ICU admission; Previous neuromuscular disease that may delay or stop the ventilatory weaning (such as severe myasthenia, amyotrophic lateral sclerosis); Hip fracture, unstable cervical or pathological fracture (patient with block mobilization)

Design outcomes

Primary

MeasureTime frame
Functionality, at ICU discharge, verified by the 7 points variation, by the FSS-ICU scale—

Secondary

MeasureTime frame
Length of stay in the ICU by counting days of ICU stay;Functionality, at ICU discharge, verified by the PFIT scale;Ventilatory weaning time defined by the number of days in mechanical ventilation;Incidence of pneumonia defined by the number of patients presenting with pneumonia during the course of the study;Incidence of deep venous thrombosis (DVT) defined by the number of patients who had DVT during the study;Incidence of delirium defined by daily CAM-ICU scale;Hospital costs assessed by the hospital beds control sector;Quality of life assessed by the EQ-5D scale;Functionality, at CTI discharge, verified by the ICU mobility scale (IMS);Muscle strength, on CTI discharge, verified by the MRC scale—

Countries

Brazil

Contacts

Public ContactMarcos Borges

Faculdade de Medicina de Ribeirão Preto

marcosborges@fmrp.usp.br+55(16)981165608

Outcome results

None listed

Source: REBEC (via WHO ICTRP)