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Clinical Trials/NCT04771598
NCT04771598
Completed
Not Applicable

EVALUATING THE EFFICIENCY OF BREATHING EXERCISES PERFORMED BY POST-COVID TELEMEDICINE: Randomized Controlled Study

Tokat Gaziosmanpasa University1 site in 1 country52 target enrollmentFebruary 25, 2021
ConditionsCovid19

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Covid19
Sponsor
Tokat Gaziosmanpasa University
Enrollment
52
Locations
1
Primary Endpoint
6 minute walking test
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

As an important non-drug intervention in the treatment of respiratory tract diseases, respiratory rehabilitation training is increasingly accepted in clinical practice. The purpose of pulmonary rehabilitation is not only to improve the physical and mental conditions of the patient, but also to help the patient return to the family and society more quickly.

In light of the widely documented lung injuries associated with COVID-19, concerns are raised regarding the assessment of lung injury in discharged patients. As an important non-drug intervention in the treatment of respiratory diseases, respiratory rehabilitation training is increasingly being accepted in clinical practice The purpose of pulmonary rehabilitation is not only to improve the physical and mental conditions of the patient, but also to help the patient return to the family and society more quickly.

The aim of the study; It is aimed to evaluate the efficiency of breathing exercise in individuals with COVID-19.

Registry
clinicaltrials.gov
Start Date
February 25, 2021
End Date
July 30, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Tokat Gaziosmanpasa University
Responsible Party
Principal Investigator
Principal Investigator

Fatih OKAN

Assist. Prof.

Tokat Gaziosmanpasa University

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or older and who received / will receive treatment with the diagnosis of COVID 19 and completed 2 months after the diagnosis of COVID 19
  • Patients who applied to the Pulmonary Diseases outpatient clinic with complaints of dyspnea
  • FEV1 / FVC \<80%, FVC \<80%, FEV1 \<80%, FEF25-75\> 50% and / or Patients with respiratory distress in daily living activities

Exclusion Criteria

  • FEV 1 \<50%, FEF 25-75 \<50% detected oxygen saturation \<85% at rest,
  • moderately severe heart failure,
  • has a disease that restricts its mobilization,
  • psychiatric illness,
  • advanced stage liver, advanced stage renal failure,
  • Myocardial infarction within 4 months
  • having a history of unstable angina
  • active infectious disease

Outcomes

Primary Outcomes

6 minute walking test

Time Frame: 1 month

6 minute walking test

FEV-1

Time Frame: 1 month

FEV-1

MVV

Time Frame: 1 month

MVV- Maximal Voluntary Ventilation

FVC

Time Frame: 1 month

FVC

FEV1/FVC

Time Frame: 1 month

FEV1/FVC

Secondary Outcomes

  • St. George's Respiratory Questionnaire(1 month)

Study Sites (1)

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