Telerehabilitation Clinical Trial
Official title:
The Effect of Telerehabilitation-Based Breathing Exercise Programs With and Without Instruments on Lung Capacity
It is a prospective randomized controlled trial. In this project, it is aimed to examine the effect of telerehabilitation-based instrumental and noninstrumental respiratory exercise program on lung capacities. For this reason; - Contributing to the literature by comparing the effect of breathing exercises with and without instruments on lung capacities, - It is aimed to be a resource for the effective use of respiratory exercise, which has a high effect on lung capacities, in treatment. In addition, with the data obtained, it is aimed to decide and apply the exercise that is more effective in the treatment of respiratory diseases quickly. Socio-demographic data will be questioned by using the Demographic Data Form; participants, age, gender, height, weight, marital status, smoking and alcohol use, presence of disease, whether they are included in a different exercise program, dyspnea, severe nausea and vomiting. The cases will be randomized into two groups: non-instrumented breathing exercises group and instrumented breathing exercises group. The physical activity status of the individuals participating in the study will be questioned using the International Physical Activity Questionnaire-Short Form (IPAQ-SF) at the beginning and end of the study. Pulmonary Function Test (PFT) will be used to measure the lung capacity of the participants. Instrumented breathing exercises will be performed for 8 weeks, 2 days a week with the telerehabilitation program, 3 days a week as a home program, 5 days a week in total, starting with 1 set of 15 repetitions and the program will progress with progression. Diaphragmatic breathing and thoracic extension exercises will be applied as non-instrumented breathing exercises. For 8 weeks, 2 days a week with telerehabilitation method, 3 days a week as a home program, 5 days a week in total, 1 set of 10 repetitions for each exercise and the program will progress with progression. At the end of 8 weeks, all evaluations of the participants in both groups will be repeated.
Status | Not yet recruiting |
Enrollment | 26 |
Est. completion date | September 29, 2024 |
Est. primary completion date | May 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 30 Years |
Eligibility | Inclusion Criteria: - Female/male young adult between the ages of 18-30 December, - Who volunteered to participate in the study, - Without a known disease - Volunteers who do not have psychological, cognitive and emotional problems Exclusion Criteria: - Cigarette and alcohol users - People with severe cardiopulmonary disorders - People with postural disorders (such as scoliosis,kyphosis...) - Unstable angina, has it been recently, pulmonary embolism - People with obesity/diabetes - Mental or cognitive impairment that will affect mental cooperation - People with severe nausea, vomiting attacks - People with dyspnea - People with orthopedic disorders that will affect exercise performance |
Country | Name | City | State |
---|---|---|---|
Turkey | University of Health Sciences | Istanbul |
Lead Sponsor | Collaborator |
---|---|
Saglik Bilimleri Universitesi |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pulmonary Function Test for FEV1 | Pulmonary function test will be performed with desktop type spirometry. The FEV1 value will be calculated. | At baseline and 8 weeks | |
Primary | Pulmonary Function Test for PEF | Pulmonary function test will be performed with desktop type spirometry. The PEF value will be calculated. | At baseline and 8 weeks | |
Primary | Pulmonary Function Test for FEV1/FVC | Pulmonary function test will be performed with desktop type spirometry. The FEV1/FVC value will be calculated. | At baseline and 8 weeks | |
Primary | Pulmonary Function Test for FVC | Pulmonary function test will be performed with desktop type spirometry. The FVC value will be calculated. | At baseline and 8 weeks | |
Secondary | International Physical Activity Questionnaire-Short Form (IPAQ-SF) | IPAQ-SF is a form designed to measure physical activity among individuals. It includes leisure time physical activities, home and garden activities, work-related physical activities, transportation-related physical activities. Physical activity status will be determined by this questionnaire. | At baseline and 8 weeks |
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