The Effects of Different Physiotherapy Approaches in Stable COPD Patients.

COPD Clinical Trial

Official title:

The Effects of Kinesio Taping, Rigid Taping, Thoracic Mobilization and Core Stabilization Approaches on Respiratory Muscle Morphology, Respiratory Muscle Strength, Exercise Capacity and Quality of Life in Stable COPD Patients.

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05335304
• Other study ID #: physiotherapy approaches
• Status: Not yet recruiting
• Phase: N/A
• Start date: April 18, 2022
• Est. completion date: May 15, 2023

Study information

• Verified date: April 2022
• Source: Mugla Sitki Koçman University
• Contact: Emine Korkmaz
• Phone: 5077476873
• Email: eminekorkmazfzt[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In our study, the effects of Kinesio Taping (KT), Rigid Taping (RT), Thoracic Mobilization (TM) and Core Stabilization (KS) approaches on respiratory muscle morphology, respiratory muscle strength, exercise capacity and quality of life will be examined in stable COPD patients. Study is designed as prospective, single-blinded, randomized-controlled study.

Description:

The study is planned to compare the effects of different physiotherapy approaches on respiratory muscle morphology, respiratory muscle strength, exercise capacity and quality of life in stable COPD patients over 18 years of age.The study is carried out on 65 patients who applied to Muğla Training and Research Hospital with COPD patients. The patients are divided into 5 groups by randomization method. First group, Kinesio Taping group, inhibitory effect on upper trapezius and scalene muscles, facilitator effect on diaphragm and intercostal muscles will be applied. The second group, Rigid Taping group, inhibitory effect on upper trapezius and scalene muscles, facilitator effect on diaphragm and intercostal muscles will be applied. The third group,Thoracic Mobilization group, Modified Active-Passive Thoracic mobilization will be performed according to the patients' conditions. Thoracic Mobilization techniques will be used to improve thoracic mobility in the upper, middle or lower parts of the chest. The fourth group,In Core Stabilization group, five different trunk stabilization exercises will be performed. Fifth group is the control group and no taping was done. A standard treatment program is applied for the individuals in the whole group. Evaluations is made before and after treatment (3 and 6 weeks). Evaluation parameters is respiratory muscle morphology, respiratory muscle strength, exercise capacity and quality of life. The respiratory muscle morphology is measured by the radiologist, and all other measurements and treatments were performed by the physiotherapist. Pulmonary function test will be measured using spirometry, respiratory muscle strength using mouth pressure device, functional exercise capacity using 6-minute walk test, quality of life using Leicester Cough Questionnaire, dyspnea using Modified Medical Research Council Dyspnea Scale and, symptoms using COPD Assessment Tests. The data obtain from the research will be analyzed using the SPSS program. Statistical significance level will be accepted as p<0.05. In the statistical difference analysis between groups, one-way ANOVA test will be used for parametric data and Kruskal- Wallis test will be used for non-parametric data.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 65
• Est. completion date: May 15, 2023
• Est. primary completion date: March 15, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. People with stable COPD,

2. Patients with spirometric measurements of GOLD 2-3 according to the new GOLD classification and A, B according to symptoms and exacerbations

3. To be 18 years or older,

4. No acute exacerbation in the last 3 weeks,

5. Alterations in medical treatment and not using any antibiotics in last 3 weeks,

6. Not being included in the pulmonary rehabilitation program in the last 6 months,

7. Volunteering to participate in study

Exclusion Criteria:

1. Orthopedic and neuromuscular disorders,

2. Advanced heart failure,

3. Aortic stenosis, deep vein thrombosis, pacemaker,

4. Patients with acute exacerbation of symptoms in the previous three weeks,

5. Those with weak cognitive function will be excluded from the study.

6. Patients who are unable to cooperate will also be considered ineligible.

7. Irritation, infection, allergic reaction, scarred burn or open wound around application area.

Related Conditions & MeSH terms

• COPD

Intervention

Other:
• intervention group 1
Kinesio taping The intervention of this experimental study is therapeutic taping (kinesio tape) on the respiratory muscles of the participants.
• intervention group 2
Rigid taping The intervention of this experimental study is therapeutic taping (rigid tape) on the respiratory muscles of the participants.
• intervention group 3
Thoracic Mobilization The intervention of this experimental study is active-passive Thoracic mobilization techniques on the on the upper, middle or lower parts of the chest of the participants
• intervention group 4
Core Stabilization The intervention of this experimental study is Core Stabilization exercises to the trunk muscles of the participants.
• Pulmonary Rehabilitation
Pulmonary Rehabilitation respiratory rehabilitation, stretching exercises, posture correction exercises

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Mugla Sitki Koçman University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Respiratory muscle morphology	Respiratory muscle morphology measurement will be made by the radiologist with the US imaging method. It will be applied to the diaphragm, intercostal muscles, upper trapezius and scalene muscles.	Change in muscle thickness at 6 week
Primary	Respiratory muscle strength	Maximum inspiratory pressure (Pimax) and maximum expiratory pressure (PEmax) will be evaluated using an electronic pressure transducer.Measurements will be made according to the guidelines of the American Thoracic Society/European Respiratory Society.; Pimax at residual volume and PEmax from Total lung capacity, Maximal inspiratory pressure will be determined by placing a nose clip instructed to exhale to residual volume followed by maximum inspiration.; To assess maximal expiratory pressure, the patient is instructed to inhale until total lung capacity is reached, followed by a forced exhalation. Three evaluations will be recorded and the best value will be used.	Change in MIP and MEP at 6 week
Primary	6-minute walk test	It will be held in a 30 m barrier-free corridor. The measurement will be made according to the guidelines of the American Thoracic Society. The 6MWT will be repeated 2 times and the result will be given as a percentage of the predicted values. Patients will rest for 30 minutes between tests and the maximum distance will be recorded.	Change in distance at 6 week
Primary	Leicester Cough Questionnaire	It consists of 19 items in 3 subcategories (physical, psychological, social) assessing the quality of life associated with chronic cough. Each question is evaluated using a 7-point Likert-type scoring system. The total score is obtained by summing the 3 sub-category scores. High scores are indicative of good quality of life.	Change in quality of life at 6 week
Secondary	Modified Borg Scale	It is a scale used to evaluate the severity of dyspnea on exertion and the severity of dyspnea at rest. It consists of ten items describing the severity of dyspnea according to their degrees. 0 scales as no dyspnea, 10 as very severe dyspnea	Change in dyspnea at 6 week
Secondary	COPD Assessment Test (CAT)	It was developed to measure the health status and to evaluate the disease effect and severity in COPD. The CAT consists of eight questions, covering problems such as shortness of breath, cough, sputum production, as well as symptoms such as fatigue and sleep problems. Perfect health: 0 points (minimum), worst health: 40 points. (max score)	Change in healty status at 6 week
Secondary	Static and dynamic lung volumes Pulmonary Function Tests	In order to evaluate pulmonary functions, FVC, FEV1, FEV1/FVC, Peak flow rate (PEF), 25-75% (FEF 25-75%) flow rate of forced expiratory volume will be taken in sitting position according to ATS/ERS criteria. Pulmonary function test parameters will be expressed as a percentage of actual values and expected values.	Change in lung volumes at 6 week.
Secondary	Modified Medical Research Council	The dyspnea scale will be used to evaluate the severity of dyspnea during activities of daily living. It will be graded from 0 (absence of dyspnea during strenuous exercise) to 4 (dyspnea during daily activities). The dyspnea perception scale will be questioned to what extent the patients have perceived dyspnea in daily activities in the last week.	Change in perception of dyspnea at 6 week
Secondary	COPD and Asthma Fatigue Scale	The original scale consists of 12 items and a Likert-type scale (1=never, 2=rarely, 3=sometimes, 4=often, 5=very often) is used for responses. Scoring of the scale is in a five-point Likert type and a total value between 12 and 60 points is obtained.	Change in fatigue score at 6 week
Secondary	Posture analysis	"Posture Screen Mobile" mobile application will be used via smart phone to evaluate static posture.	Change in posture at 6 week
Secondary	Chest anterior-posterior diameter measurement	Rib cage measurements Anterior and posterior diameter will be measured using a caliper.	Change in chest diameter at 6 week