Status:
COMPLETED
The Effectiveness Pulmonary Telerehabilitation and Cognitive Telerehabilitation in COPD Patients
Lead Sponsor:
Saglik Bilimleri Universitesi
Conditions:
Severe Chronic Obstructive Pulmonary Disease
Dyspnea
Eligibility:
All Genders
40-80 years
Phase:
NA
Brief Summary
The aim of our study is to compare the effectiveness of the supervized pulmonary telerehabilitation program and the cognitive telerehabilitation method, which includes pulmonary telerehabilitation met...
Detailed Description
The demographic information of the participants who accepted to participate in the study by reading and signing the voluntary consent form will be questioned with the demographic data form to be creat...
Eligibility Criteria
Inclusion
- Volunteering to participate in the study
- Being diagnosed with C and D group COPD according to GOLD (Global iniative for chronic Obstructive Lung Disease) staging
- Not using an assistive device
- Using the same drugs for the last 4 weeks
- Permission to participate in the exercise for the patient from the responsible physician
- Getting a score of 24 or higher in the Standardized Mini Mental State Examination (MMDM)
- Absence of additional comorbid diseases of the orthopedic, neurological, cardiac system
- Having a score of 30 or higher on each of the Kinesthetic and Visual Imagery Questionnaire -20 (KGIA-20) visual imagery score and kinesthetic imagery score
Exclusion
- Refusing to participate in the study
- Presence of respiratory system disease other than COPD
- Contraindication for moderate-intensity exercise (eg, unstable heart disease or stage 2 hypertension)
- Being an active smoker
- Patients who have had an acute exacerbation of COPD in the last 4 weeks
- Patients who have used oral corticosteroid drugs in the last 4 weeks
- Internet, computer, etc. patients who do not have technological equipment
- Patients who had a COPD exacerbation during the study protocol
- Participants who cannot understand verbal instructions and are visually impaired
- Having participated in another clinical trial within the last 30 days and currently that could affect the results of the trial.
Key Trial Info
Start Date :
January 31 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 24 2023
Estimated Enrollment :
26 Patients enrolled
Trial Details
Trial ID
NCT05222295
Start Date
January 31 2022
End Date
February 24 2023
Last Update
April 11 2023
Active Locations (1)
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1
Yedikule Chest Disease Hospital
Istanbul, Zeytinburnu, Turkey (Türkiye), 34200