- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05922293
Combined Effects of Blow Bottle Technique and Percussion Technique in COPD Patients
Combined Effects of Blow Bottle Technique and Percussion Technique in Patients With Chronic Obstructive Pulmonary Disease
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Chronic obstructive pulmonary disease (COPD) is characterized by nonreversible airway obstruction. A diagnosis of COPD is determined by clinical assessment of airflow limitation and symptoms such as cough and wheeze; however, the detrimental effect of COPD symptoms on a patient's quality of life (QoL) is often underestimated. Rehabilitation exercise can lessen the possibility of the progressive exacerbation of the patient's condition, exerting an active role in improving their lung function and the quality of the patients' life. Therefore, a lung function exercise bottle is designed, which is capable of adjusting the pressure according to the patient's needs. The exercise bottle is composed of three components, including bottle body, threaded round cap and air blow pipe. Furthermore, manual chest percussion is the rhythmic clapping on the chest wall with relaxed wrist and cupped hand, creating an energy wave that is transmitted to the airways. It is applied with a frequency of approximately 3-6 Hz. To reduce any adverse consequences, the technique should be performed for about 30 seconds and simultaneously with no more than three or four lower thoracic expansion exercises.
It will be a randomized control trial. Participants will be recruited according to inclusion criteria and will be allocated into 2 groups using convenience sampling technique. Group 1 will be treated with percussion technique for 30 min and group 2 with blow bottle technique combined with percussion technique for 30 min at DHQ Teaching Hospital Gujranwala. Intervention will be carried out for total 4 weeks of duration with 3 sessions per week. Outcome measures such as dyspnea, breathlessness, sputum and cough, O2 and pulse rate, expiratory flow rate will be measured by tools as mMRC, BCSS, peak flow meter respectively. Assessment will be done before and after intervention and result will be analyzed using statistical package for social sciences SPSS 20.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Punjab
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Gujranwala., Punjab, Pakistan, 54560
- DHQ Teaching Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Mild-to-Moderate COPD (according to GOLD criteria)
- Both gender (male and female)
- Aged between 35 and 80 years
Exclusion Criteria:
- Clinically unstable
- cardiovascular impairment,
- musculoskeletal dysfunction
- neurological disease
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 |
|---|---|
|
Active Comparator: Blow Bottle technique
Blowing with a straw into a water bottle is a good exercise to improve breathing capacity.
The user, who has poor pulmonary function, always has his "blow bottle" handy
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When you blow through a tube into water in a bottle, the pressure in the airways increases.
This opens up the passageways between bronchioles, allowing air to flow behind the mucus and push it into the larger airways.
This way, it will be easy to remove the mucus by coughing or huffing.
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Experimental: percussion
Percussion technique should be performed for about 30 seconds and simultaneously with no more than three or four lower thoracic expansion exercises
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When you blow through a tube into water in a bottle, the pressure in the airways increases.
This opens up the passageways between bronchioles, allowing air to flow behind the mucus and push it into the larger airways.
This way, it will be easy to remove the mucus by coughing or huffing.
Percussion technique should be performed for about 30 seconds and simultaneously with no more than three or four lower thoracic expansion exercises.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dyspnea (Modified Medical Research council)
Time Frame: fourth week
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The mMRC grade is a five-point scale based on the degree of dyspnea a patient.
The use of this scale to evaluate symptoms is encouraged by current standards
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fourth week
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Breathlessness, cough and sputum scale (BCSS)
Time Frame: fourth week
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In order to give a rapid and simple means of assessing the severity of respiratory symptoms frequent in COPD patients, the Breathlessness, Cough, and Sputum Scale (BCSS) was created.
The BCSS is based on a three-item questionnaire that evaluates the patient's sputum production, coughing, and breathlessness
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fourth week
|
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Expiratory flow rate (peak flow meter)
Time Frame: fourth week
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A peak flow rate should be used to capture the highest flow rates.
The patient must record the highest reading out of a possible three.
The best at the moment is this.
A typical chart has dates with AM and PM times, a left margin, and a scale that ranges from 0 litres per minute at the bottom to 600 litres per minute at the top
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fourth week
|
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O2 n pulse rate by Oximeter
Time Frame: fourth week
|
A pulse oximeter measures the amount of oxygen that is carried by your blood.
Typically, a little clip is attached to the tip of your finger.
(On sometimes, the toe or earlobe are used.)
A light beam is projected through the skin using the gadget.
By measuring the proportion of your blood that is carrying oxygen, it calculates your oxygen level.
Your oxygen saturation, often known as SpO2, is displayed on the screen
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fourth week
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sidra Afzal, PP-DPT, Riphah International University
Publications and helpful links
General Publications
- Jones PW, Watz H, Wouters EF, Cazzola M. COPD: the patient perspective. Int J Chron Obstruct Pulmon Dis. 2016 Feb 19;11 Spec Iss(Spec Iss):13-20. doi: 10.2147/COPD.S85977. eCollection 2016.
- Raherison C, Girodet PO. Epidemiology of COPD. Eur Respir Rev. 2009 Dec;18(114):213-21. doi: 10.1183/09059180.00003609.
- Liu H, Zhang X, Zhang Y. [Design and application of a pulmonary function exercise bottle]. Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2019 Feb;31(2):236-237. doi: 10.3760/cma.j.issn.2095-4352.2019.02.023. Chinese.
- Celli BR. Update on the management of COPD. Chest. 2008 Jun;133(6):1451-1462. doi: 10.1378/chest.07-2061. Erratum In: Chest. 2008 Oct;134(4):892.
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 (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR&AHS/23/0320
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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