- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03496376
Effects of Thoracic Kinesio Taping on COPD Patients
Effects of Thoracic Kinesio Taping on Pulmonary Functions, Respiratory Muscle Strength and Functional Capacity in COPD Patients
The purpose of this study was to investigate the effect of kinseio taping on functional capacity, pulmonary functions, respiratory muscle strength, severity of dyspnea, severity of fatigue in Chronic Obstructive Pulmonary Disease (COPD). Assessment of patients was done baseline and 6th week.
Eligible patients for the study randomly allocated to Kinesio Taping Group (KTG), or Control Group (CG). Both groups received three different deep breathing exercises (diaphragmatic, thoracic, and lateral basal), each consisting of three sets of 10 repetitions, with 30 seconds of rest between each set. KTG also received thoracic kinesio taping application.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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İzmir, Turkey, 35340
- Dokuz Eylül Üniversitesi School of Physical Therapy and Rehabilitation
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- aged 40 years and older,
- having stage II-III COPD diagnosis according to GOLD system and BODE Index by chest physician,
- unwilling to participate in any kind of pulmonary rehabilitation program for COPD,
- able to read, write, and understand Turkish; and
- willing and able to attend the study.
Exclusion Criteria:
- being in COPD exacerbation period,
- having neurological or musculoskeletal problems that would affect physical mobility,
- having unstable, severe heart disease(s) (heart failure, unstable hypertension, previous angina pectoris or myocardial infarction, heart valve problems),
- having scar, lesion or incision in the area of kinesio tape application,
- previous use of kinesio tape,
- having skin sensitivity against kinesio tape,
- malignancy,
- having mental and cognitive disorders that would affect cooperation.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Kinesio Taping Group
Kinesio Taping Group received three different deep breathing exercises (diaphragmatic, thoracic, and lateral basal), each consisting of three sets of 10 repetitions, with 30 seconds of rest between each set plus thoracic kinesio taping application.
|
The material used for thoracic kinesio taping application was Kinesio® Tex Gold™ (Kinesio Holding.
Patients were instructed to sit upright on an armless chair with no back support, with knees flexed to 90 degrees, feet on the floor and arms relaxed.
Kinesio tape was applied anteriorly and posteriorly to facilitate respiratory muscles (primarily diaphragm) along the subcostal area.
Additionally, two more kinesio tapes were applied to upper trapezius and scalene muscles' area which lies between neck and acromion at both sides (left and right).
Three different deep breathing exercises (diaphragmatic, thoracic, and lateral basal), each consisting of three sets of 10 repetitions, with 30 seconds of rest between each set.
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Active Comparator: Control Group
Control Group received three different deep breathing exercises (diaphragmatic, thoracic, and lateral basal), each consisting of three sets of 10 repetitions, with 30 seconds of rest between each set.
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Three different deep breathing exercises (diaphragmatic, thoracic, and lateral basal), each consisting of three sets of 10 repetitions, with 30 seconds of rest between each set.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change in functional capacity
Time Frame: Baseline, 6th week
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Six-minute walk test (6MWT) is a valid, reliable and useful test for assessing functional capacity of COPD patients.
This test assesses distance walked over 6 minutes as a sub-maximal test of aerobic capacity/endurance.
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Baseline, 6th week
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change in pulmonary functions
Time Frame: Baseline, 6th week
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Pulmonary function test (PFT) is a generic term used to indicate a battery of studies or maneuvers that may be performed using standardized equipment to measure lung function.
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Baseline, 6th week
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Change in respiratory muscle strength
Time Frame: Baseline, 6th week
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Measurement of respiratory muscle strength is useful in order to detect respiratory muscle weakness and to quantify its severity.
Respiratory muscle strength is assessed by mouth pressures sustained for 1 s during maximaş static manoeuvre against a closed shutter.
|
Baseline, 6th week
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Change in severity of dyspnoea
Time Frame: Baseline, 6th week
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Modified Medical Research Council (mMRC) dyspnea scale is a valid and reliable test for measuring the severity of dyspnea of COPD patients.
This scale ranges from 0 to 4. A higher value represents a worse outcome.
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Baseline, 6th week
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Change in severity of fatigue
Time Frame: Baseline, 6th week
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Modified Borg Scale (MBS) is a useful scale for severity of fatigue.
This scale ranges from 0 to 10.
A higher value represents a worse outcome (0=not at all, 10=maximal).
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Baseline, 6th week
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 1925-GOA
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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