Skip to main content
Clinical Trials/NCT04771598
NCT04771598CompletedNot Applicable

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

Tokat Gaziosmanpasa University1 site in 1 country52 target enrollmentStarted: February 25, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
52
Locations
1
Primary Endpoint
6 minute walking test

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

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

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)

Investigators

Sponsor
Tokat Gaziosmanpasa University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Fatih OKAN

Assist. Prof.

Tokat Gaziosmanpasa University

Study Sites (1)

Loading locations...

Similar Trials