The Effectiveness Pulmonary Telerehabilitation and Cognitive Telerehabilitation in COPD Patients
- Conditions
- Severe Chronic Obstructive Pulmonary DiseaseDyspneaFunctional CapacityQuality of LifePulmonary DiseaseMuscle WeaknessRespiratory DiseaseFatigueMuscle StrengthMotor Imagery
- Interventions
- Other: Supervised Pulmonary TelerehabilitationOther: Cognitive Telerehabilitation
- Registration Number
- NCT05222295
- Lead Sponsor
- Saglik Bilimleri Universitesi
- 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 methods, in patients with severe stage COPD who have difficulty exercising heavily. The effects of pulmonary and cognitive rehabilitation on dyspnea, muscle strength, functional capacity, quality of life, anxiety and depression levels in this patient group will be examined.
The number of studies in the literature in which the pulmonary rehabilitation program was applied as telerehabilitation is insufficient. Considering that this patient group is not motivated and has difficulty in exercising, motor imagery and movement observation methods from cognitive rehabilitation methods may be alternative methods for these patients. Although these methods have been very popular in recent years in terms of researching and demonstrating their effectiveness in various patient groups in the literature, no study has been found in which the effects of these methods have been applied in pulmonary disease groups. This study aims to contribute to the serious gap in the literature on the application of pulmonary telerehabilitation and its effectiveness, and to be an original study by investigating the effectiveness of motor imagery and action observation, which are popular rehabilitation methods of recent years, in COPD patients in the pulmonary disease group for the first time.
- 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 created by the researchers. The patients' dyspnea status will be evaluated with the Modified Medical Research Council Dyspnea Scale, and their exercise capacity will be evaluated with the 6-minute walk test (6 MWT). Modified Borg Scale will be used to determine dyspnea and leg fatigue before and after 6MWT, and a digital sphygmomanometer will be used to measure blood pressure. Before, during and after the test, saturation and heart rate will be determined by finger pulse oximetry. Blood lactate levels will be determined with a portable lactate meter. An electronic hand dynamometer will be used to measure peripheral muscle strength. Activities of daily living will be assessed with the London Chest Activity of Daily Living Scale. Quality of life will be determined by The Saint George Respiratory Questionnaire, and anxiety and depression status will be determined by the Hospital Anxiety and Depression Scale. Muscle activities will be analyzed using a surface electromyographic (EMG) measuring device. The mental imagery abilities of the patients will be evaluated with the Kinesthetic and Visual Imagery Questionnaire-20 and the mental chronometry method.
Evaluations will be made by the responsible physiotherapist at the hospital before the program, at the end of the 4th week and at the end of the 8th week of the program. The permissions for the use of the questionnaires to be used were obtained from the authors, who made the validity and reliability in Turkish, via e-mail. Ethical approval of the study was obtained from the Ethics Committee of Istanbul Yedikule Chest Diseases and Thoracic Surgery Training and Research Hospital.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 26
- 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
- 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.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Supervised Pulmonary Telerehabilitation Group Supervised Pulmonary Telerehabilitation Three times a week for 8 weeks, a supervised and standardized pulmonary rehabilitation program will be applied in the form of telerehabilitation with simultaneous video conference method, accompanied by a specialist physiotherapist, while the patients are at home. Cognitive Telerehabilitation Group Cognitive Telerehabilitation Motor imagery + action observation methods will be applied. In therapy, a video recording of each exercise in the supervised telerehabilitation group will be sent to the patients by the physiotherapist in accordance with the number of repetitions. At the end of the session, the cognitive telerehabilitation group will be asked to actively do the breathing exercises and active breathing techniques cycle in the supervised telerehabilitation group as well as to imagine with the instructions in the video recording, and commands will be given accordingly.
- Primary Outcome Measures
Name Time Method Perception of dyspnea Change from baseline dyspnea level at 8 weeks The patients' dyspnea status will be evaluated with the Modified Medical Research Council Dyspnea Scale (mMRC Dyspnea Scale). he severity of dyspnea is rated on a scale of 0 to 4. "0" means no dyspnea perception, "4" means severe dyspnea perception.
Peripheral muscle strength Change from baseline peripheral muscle strength at 8 weeks An electronic hand dynamometer will be used to measure peripheral muscle strength.
The exercise capacity Change from baseline functional capacity at 8 weeks The exercise capacity will be evaluate by the 6 minute walking test (6MWT).The test was conducted in a 30-meter corridor in line with American Thoracic Society (ATS) guidelines.
- Secondary Outcome Measures
Name Time Method Respiratory muscle activity Change from baseline accessory respiratory muscle activity at 8 weeks Main and accessory respiratory muscle activity will be analyzed using an electromyographic (EMG) measuring device.
Kinesthetic and Visual Imagery Questionnaire-20 Change from baseline imagery abilities level at 8 weeks Patients' mental imagery abilities will be assessed with the Kinesthetic and Visual Imagery Questionnaire-20. With the questionnaire, the intensity level of the imagery is recorded on a 5-point Likert scale (Visual imagery; 5= As clear as the original, 4: Quite clear, 3= Medium sharp, 2= Blurred, 1= No image) (Kinesthetic imagery; 5= As intense as if you were doing the movement) , 4 = Fairly intense, 3 = Moderately intense, 2 = Slightly intense, 1 = no sensation).
Mental chronometry method Change from baseline imagery abilities between real time and imagery time level at 8 weeks Patients' mental imagery abilities will be assessed with mental chronometry method.
Blood Lactate Measurement Change from baseline blood lactate level at 8 weeks Measurement will be made from the middle finger with a portable blood lactate meter.
the London Chest Activity of Daily Living Scale Change from baseline activities of daily living at 8 weeks Activities of daily living (ADL) will be assessed with the London Chest Activity of Daily Living Scale. Each item is scored from 0 to 5, and higher scores indicate greater difficulty in performing the ADL.
The Saint George Respiratory Questionnaire (SGRQ) Change from baseline quality of life at 8 weeks Quality of life will be determined by The Saint George Respiratory Questionnaire. Scores range from 0-100. A score of zero indicates normal and a score of 100 indicates maximum disability. In the SGRQ questionnaire, four units of treatment-related change are considered significant.
the Hospital Anxiety and Depression Scale Change from baseline anxiety and depression status at 8 weeks Anxiety and depression status will be determined by the Hospital Anxiety and Depression Scale. The items in the scale are evaluated with a 4-point Likert scale and are based on a scoring system between 0-3. According to the scoring, 0-1 is considered as non-patient, 2 as borderline patients, and 2-3 as severely ill.
Trial Locations
- Locations (1)
Yedikule Chest Disease Hospital
🇹🇷Istanbul, Zeytinburnu, Turkey