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Clinical Trials/NCT04603963
NCT04603963TerminatedNot Applicable

Efects of Inspiratory Muscle Training in Patients With COVID-19 After Acute Phase. Prospective Study

Elaine Cristina Pereira <elaine.cpereira@einstein.br>1 site in 1 country55 target enrollmentStarted: June 1, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Sponsor
Enrollment
55
Locations
1
Primary Endpoint
impact on functionality

Study Overview

Brief Summary

COVID 19 has become a pandemic and has led to high demand on healthcare systems. It can cause a severe acute respiratory syndrome (SARS CoV-2) which leads to a long hospital stay, developing important functional damage and making hospital discharge difficult. Elderly, obese and people with chronic diseases are more susceptible to contracting the disease, this profile of patients already has a predisposition for respiratory muscle weakness and in this context, after clinical stability, it is still necessary in a hospital environment to approach respiratory and motor physiotherapy. to optimize the recovery of these patients. Objective: Improved breathing, functionality, exercise capacity and muscle strength in non-critical patients. Method: Prospective randomized clinical study where one group received motor and respiratory physiotherapy and the other group performed the same therapy associated with inspiratory muscle training. Results: The findings will be compared before and after the approach and will be presented in graphs and tables. Statistical tests will be used considering a significance level of 5%.

Detailed Description

Prospective clinical study in patients with COVID-19 admitted to a non-critical unit of a tertiary hospital. They were randomized into a group that received motor and respiratory exercises and another group that received the same exercises associated with respiratory muscle training.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Investigator)

Masking Description

Stratified randomization was performed in which the impaired chest tomography (absent, less than 50% or greater than 50%)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •patients diagnosed with COVID-19 through PCR aged over 18 years admitted to non-critical units.

Exclusion Criteria

  • •patients with changes in the level of consciousness and non-transient understanding, exclusive palliative care without prognosis.

Arms & Interventions

group control

No Intervention

alternate exercises: in one day breathing exercises, active or with a load of large muscle groups (according to tolerance) with a maximum limit of 2 kg, sedation out of bed, walking. On another day aerobic exercise with cycle ergometer limited to 30 minutes.

intervention group

Experimental

He received the same intervention as the control group, associating respiratory muscle training 1 time a day with power breathe 3 series of 10 repetitions (started with 30% of the Pimax value) with readjusted load every 7 days.

Intervention: power breathe (Device)

Outcomes

Primary Outcomes

impact on functionality

Time Frame: 14 days

respiratory muscle training appears to impact functionality

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Elaine Cristina Pereira <elaine.cpereira@einstein.br>
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Elaine Cristina Pereira <elaine.cpereira@einstein.br>

physiotherapist

Hospital Israelita Albert Einstein

Study Sites (1)

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