Effect of Critical Patients Mobilization on Respiratory and Peripheral Muscle Strength and Functional Capacity.

NCT ID: NCT02919085

Last Updated: 2021-08-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-12-31

Study Completion Date

2017-12-31

Brief Summary

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To analyze changes on respiratory muscle strength, peripheral and functional capacity of critically ill patients with clinical and surgical etiology, breathing spontaneously and bedridden, within 48 hours of admission to the intensive care unit (ICU) and if there are correlations among these variables. This is an observational study. Respiratory muscle strength will be assessed through the maximum inspiratory pressure (MIP) and maximal expiratory pressure (MEP) and peripheral muscle strength, by the Medical Research Council score (MRC) and hand grip test and functional capacity through the Functional Independence Measure (FIM) and Physical Function ICU Test Score (PFIT-s) in the period between 24h and 48h of hospitalization in the adult ICU. For descriptive purposes, the sample will be stratified according to clinical and surgical characteristics. Correlations will be determined using the Pearson test, with significance level of p \<0.05.

Detailed Description

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Conditions

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Intensive Care Unit Syndrome Muscle Weakness

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Mobilization

Group Type EXPERIMENTAL

Early ambulation

Intervention Type PROCEDURE

Procedure to accelerate the ability of a patient to walk or move about by reducing the time to ambulation. It is characterized by a shorter period of hospitalization or recumbency than is normally practiced.

Interventions

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Early ambulation

Procedure to accelerate the ability of a patient to walk or move about by reducing the time to ambulation. It is characterized by a shorter period of hospitalization or recumbency than is normally practiced.

Intervention Type PROCEDURE

Other Intervention Names

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Early mobilization

Eligibility Criteria

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Inclusion Criteria

* Breathing spontaneously
* Length of stay in ICU greater than 24 hours
* Adherence to study

Exclusion Criteria

* Patients with poor prognosis or palliation;
* Preexisting neuromuscular diseases;
* Immobility or restriction to bed prior to admission;
* Nonunions and amputations;
* Osteomioarticular, cognitive or neurological impairment;
* Non-cooperation;
* Specific contraindications to the application of evaluation methods;
* Hemodynamic or respiratory instability within 48 hours of ICU admission preventing evaluation muscle strength and functional capacity.
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Universidade Federal de Pernambuco

OTHER

Sponsor Role lead

Responsible Party

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Maria Karoline de França Richtrmoc

Master student

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Maria KF Richtrmoc

Role: PRINCIPAL_INVESTIGATOR

Universidade Federal de Pernambuco

Locations

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Real Hospital Português de Beneficência

Recife, Pernambuco, Brazil

Site Status

Countries

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Brazil

References

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Williams TA, Dobb GJ, Finn JC, Webb SA. Long-term survival from intensive care: a review. Intensive Care Med. 2005 Oct;31(10):1306-15. doi: 10.1007/s00134-005-2744-8. Epub 2005 Aug 24.

Reference Type RESULT
PMID: 16132895 (View on PubMed)

Rossi PJ, Edmiston CE Jr. Patient safety in the critical care environment. Surg Clin North Am. 2012 Dec;92(6):1369-86. doi: 10.1016/j.suc.2012.08.007. Epub 2012 Oct 6.

Reference Type RESULT
PMID: 23153874 (View on PubMed)

Neideen T. Monitoring devices in the intensive care unit. Surg Clin North Am. 2012 Dec;92(6):1387-402. doi: 10.1016/j.suc.2012.08.010. Epub 2012 Oct 13.

Reference Type RESULT
PMID: 23153875 (View on PubMed)

Other Identifiers

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01110031483

Identifier Type: -

Identifier Source: org_study_id

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