Comparative Effects of BBT and Active Cycle of Breathing Technique on Dyspnea and Quality of Life in COPD
NCT ID: NCT05947253
Last Updated: 2023-07-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
40 participants
INTERVENTIONAL
2023-05-15
2023-12-15
Brief Summary
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Detailed Description
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A randomized clinical trial will be conducted using convenient sampling or randomized sampling technique in population of chronic obstructive pulmonary disease (COPD).Total sample size will be of 40 and two Groups will be made Group A 20 participants received Buyteko breathing technique and Groups B 20 participants received Active cycle of breathing technique. Data will be collected by using Borg's dyspnea scale, St.George Respiratory questionnaire and by pulmonary function testing. Data will be collected from pulmonary ward Jinnah hospital Lahore whole study will take total duration of 10 months and data will be analyzed using latest version of SPSS-25 software.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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BUTYEKO BREATHING TECHNIQUE
First Group A 20 participants received Buyteko breathing technique while will be given 5 days per week
Buyteko breathing technique
group A 20 participants received Buyteko breathing technique 2 session for 3 weeks
active cycle of breathing technique
Group B 20 participants received active cycle of breathing technique and session of 35min will be given 5 days per week
active cycle of breathing technique
Group B 20 participants received active cycle of breathing technique 2 session for 3 weeks
Interventions
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Buyteko breathing technique
group A 20 participants received Buyteko breathing technique 2 session for 3 weeks
active cycle of breathing technique
Group B 20 participants received active cycle of breathing technique 2 session for 3 weeks
Eligibility Criteria
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Inclusion Criteria
* PFT showing irreversible airflow limitation.
* Patients hemodynamically stable.
* Males and females.
* Patients capable of completing IPAQ questionnaire
Exclusion Criteria
* Disabling diseases which prevented participation in the exercise program, such as orthopedic inabilities or peripheral vascular disease.
* Systemic illness.
* Resting O2 saturation \<90% with room air breathing and Patient with viral infection
50 Years
70 Years
ALL
No
Sponsors
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Riphah International University
OTHER
Responsible Party
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Principal Investigators
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Sidra Faisal, MS.CPPT
Role: PRINCIPAL_INVESTIGATOR
Riphah International University
Locations
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Pulmonary ward Jinnah hospital Lahore.
Lahore, Punjab Province, Pakistan
Countries
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Central Contacts
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Facility Contacts
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References
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Vogelmeier CF, Roman-Rodriguez M, Singh D, Han MK, Rodriguez-Roisin R, Ferguson GT. Goals of COPD treatment: Focus on symptoms and exacerbations. Respir Med. 2020 May;166:105938. doi: 10.1016/j.rmed.2020.105938. Epub 2020 Mar 21.
May SM, Li JT. Burden of chronic obstructive pulmonary disease: healthcare costs and beyond. Allergy Asthma Proc. 2015 Jan-Feb;36(1):4-10. doi: 10.2500/aap.2015.36.3812.
Halpin DM, Miravitlles M. Chronic obstructive pulmonary disease: the disease and its burden to society. Proc Am Thorac Soc. 2006 Sep;3(7):619-23. doi: 10.1513/pats.200603-093SS.
Fazleen A, Wilkinson T. Early COPD: current evidence for diagnosis and management. Ther Adv Respir Dis. 2020 Jan-Dec;14:1753466620942128. doi: 10.1177/1753466620942128.
Smith MC, Wrobel JP. Epidemiology and clinical impact of major comorbidities in patients with COPD. Int J Chron Obstruct Pulmon Dis. 2014 Aug 27;9:871-88. doi: 10.2147/COPD.S49621. eCollection 2014.
Lopez AD, Shibuya K, Rao C, Mathers CD, Hansell AL, Held LS, Schmid V, Buist S. Chronic obstructive pulmonary disease: current burden and future projections. Eur Respir J. 2006 Feb;27(2):397-412. doi: 10.1183/09031936.06.00025805. No abstract available.
Other Identifiers
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REC/RCR & AHS/22/0318
Identifier Type: -
Identifier Source: org_study_id
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