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Clinical Trials/NCT05903144
NCT05903144
Completed
Not Applicable

Influence of Manual Diaphragm Release Combined With Conventional Breathing Exercises and Prone Positioning on Pulmonary Functions in Women With COVID-19

Cairo University1 site in 1 country40 target enrollmentJuly 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COVID-19 Pneumonia
Sponsor
Cairo University
Enrollment
40
Locations
1
Primary Endpoint
forced vital capacity FVC
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Manual noninvasive respiratory techniques gained interest to treat respiratory pathologies related to COVID 19. This study designed to determine the combined effect of manual diaphragmatic release technique with the effect of conventional breathing exercises and prone positioning on pulmonary function parameters (FVC, FEV1, PEF, FEV1/FVC, FEF25, FEF50, FEF75, FEF25/75).

Detailed Description

Forty females were randomly assigned to two groups. Group A received manual diaphragm release with conventional breathing exercises and prone positioning. Group B received conventional breathing exercises and prone positioning. Both groups took their prescribed medications. Their ages ranged from 35 to 45 years and with moderate COVID-19 illness. Any cases with mild and severe COVID-19 illness, ICU admission, and chest diseases were excluded. Main measures: pulmonary function parameters (FVC, FEV1, PEF, FEV1/FVC, FEF25, FEF50, FEF75, FEF25/75).

Registry
clinicaltrials.gov
Start Date
July 1, 2022
End Date
May 30, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

mona abd el raouf ghallab

lecturer at faculty of physical therapy

Cairo University

Eligibility Criteria

Inclusion Criteria

  • women with moderate COVID-19 illness diagnosed by a physician.
  • Patients with o2 saturation \>94%Nonsmoker subjects.
  • age ranging from 35-45 years.
  • body mass index from 25 to 34 kg/m2.

Exclusion Criteria

  • Unstable hemodynamic status.
  • Acute respiratory failure requiring intubation and impaired consciousness.
  • Inability to collaborate with prone positioning with refusal.
  • Change of mental status hindering response to instructions.
  • Poorly controlled hypertension (Mean systolic BP \> 140 mmhg and \\or diastolic BP \> 40 mmhg).
  • Patients who take continuous o2 supplementation.
  • Other chest diseases as (COPD-asthma-tuberculosis-cancer).
  • Male patients.

Outcomes

Primary Outcomes

forced vital capacity FVC

Time Frame: pre study and 3 weeks post study for all participants

the amount of air that can be forcibly exhaled from your lungs after taking the deepest breath possible which is a common breathing test to check lung function.

FEV1/FVC

Time Frame: pre study and 3 weeks post study for all participants

FEV1/FVC, also known as FEV1%) can help distinguish obstructive and restrictive lung diseases.

FEV1

Time Frame: pre study and 3 weeks post study for all participants

the maximum amount of air that the subject can forcibly expel during the first second following maximal inhalation

PEF

Time Frame: pre study and 3 weeks post study for all participants

show the amount and rate of air that can be forcefully breathed out of the lungs.

PEF25%

Time Frame: pre study and 3 weeks post study for all participants

Peak expiratory flow at 25% of fvc and the most sensitive measure of airflow in peripheral airways where primary airflow obstruction originates.

PEF50%

Time Frame: pre study and 3 weeks post study for all participants

Peak expiratory flow at 50% ofFVC

PEF 75%

Time Frame: pre study and 3 weeks post study for all participants

Peak expiratory flow at 75% of FVC

PEF 25%/75%

Time Frame: pre study and 3 weeks post study for all participants

Maximum flow rate in the middle 50% of forced expiration.

Study Sites (1)

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