Chronic Obstructive Pulmonary Disease Clinical Trial
— COPDOfficial title:
Effects of Thoracic Kinesiotaping on Pulmonary Function and Functional Capacity of COPD Patients
Verified date | February 2023 |
Source | Riphah International University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is designed to determine the effects of diaphragmatic kinesiotaping (KT) facilitation technique on pulmonary function, functional capacity and forward head posture of chronic obstructive lung diseases (COPD) patients. The application of KT as an adjunct to conventional protocol in COPD patients if proven effective can enhance the symptom control in COPD patients for improving lung function, posture reducing the perception of dyspnea as well as improving functional capacity.
Status | Completed |
Enrollment | 46 |
Est. completion date | December 28, 2022 |
Est. primary completion date | December 15, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 30 Years to 70 Years |
Eligibility | Inclusion Criteria: - Diagnosed patients of COPD falling in stage I-III according to The Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria. - GOLD 1 -mild: Forced Expiratory Volume in 1 sec (FEV1) =80%, GOLD 2 - moderate: 50% = FEV1 <80% predicted and GOLD 3 - severe: 30% = FEV1 <50% predicted - Age between 40-70 years. - Both genders - Volunteering to participate in study Exclusion Criteria: - COPD exacerbation within last 4 weeks - Allergic reaction to the taping material, - Patients with recent chest wall trauma, surgery, deformity having scar, lesion, or incision in area of KT application. - Uncontrolled arterial hypertension and diabetes mellitus. - Patients with neurological, musculoskeletal, cardiac, pulmonary disease with physical impairment and history of psychiatric illness |
Country | Name | City | State |
---|---|---|---|
Pakistan | Pak Medical Center Hospital | Peshawar | Khyber Pukhtunkhwa |
Lead Sponsor | Collaborator |
---|---|
Riphah International University |
Pakistan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Peak expiratory flow rate (PEFR) Peak expiratory flow rate (PEFR) | Peak expiratory flow rate (PEFR) Peak expiratory flow rate (PEFR) measured through digital spirometer. Peak Expiratory Flow Rate (PEFR) measured through digital spirometer. Three zones of measurement are commonly used to interpret peak flow rates. Normal value of PEFR is (80-100%). Green zone indicates 80 to 100 percent of the usual or normal peak flow reading, yellow zone indicates 50 to 79 percent of the usual or normal peak flow readings, and red zone indicates less than 50 percent of the usual or normal peak flow readings.
Changes in PEFR from baseline to 5th and after 15th day of intervention will be assessed. |
15 days | |
Primary | Forced vital capacity (FVC) | Forced vital capacity (FVC) measured through digital spirometer. If the value of FVC is within 80% of the reference value, the results are considered normal.
Changes in FVC from baseline to 5th and after 15th day of intervention will be assessed. |
15 days | |
Primary | Forced expiratory volume in 1sec (FEV1) | Forced expiratory volume in 1sec (FEV1) measured through digital spirometer. If the value of FEV1 is within 80% of the reference value, the results are considered normal.
Changes in FEV1 from baseline to 5th and after 15th day of intervention will be assessed. |
15 days | |
Primary | FVC/FEV1 | FVC/FEV1 measured through digital spirometer. The normal value for the FEV1/FVC ratio is 70% (and 65% in persons older than age 65).
Changes in FVC/FEV1 from baseline to 5th and after 15th day of intervention will be assessed. |
15 days | |
Primary | Six-minute walk test (6MWT) | The six-minute walk test (6MWT) is a submaximal exercise test for assessing physical functional capacity in patients with COPD.
It is a test that measures how far a person can walk in 6 minutes. Changes in 6MWT from baseline to 5th and after 15th day of intervention will be assessed. |
15 days | |
Primary | Modified Medical Research Council Dyspnea Scale (mMRC) | The mMRC dyspnea score is a 5-point (0-4) scale based on the severity of dyspnea.
0, no breathlessness except on strenuous exercise and and 4, too breathless to leave the house, or breathless when dressing or undressing. Changes in mMRC scale from baseline to 5th and after 15th day of intervention will be assessed. |
15 days | |
Secondary | Craniovertebral angle (CVA) | CVA is measured by taking 2 lateral photographs of the subject in a relaxed seated position without a back support. Spinous process of C7 and the tragus of ear are marked with a body marker. A horizontal line is drawn passing through C7 making a right angle with the vertical. Then, the angle between the line connecting C7 spinous process with the tragus of the ear and the horizontal line, is measured using goniometer.
Craniovertebral angle of less than 50 degrees while standing is commonly considered forward head posture. It will be assessed from baseline to 5th day and after 15th day of intervention. |
15 days |
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