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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06463288
Other study ID # REC/ 31831 Iqra
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 20, 2023
Est. completion date December 10, 2023

Study information

Verified date June 2024
Source Riphah International University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison of Jacobson Relaxation Technique and Pranayama Technique in patients with COPD


Description:

Chronic obstructive pulmonary disease is a chronic inflammatory lung disease that cause obstructed airflow from the lungs. Symptoms include Breathing difficulty. cough, mucus production and wheezing. Its typically caused by long term exposure to irritating gasses or particulate matter, most often from cigarette smoker. in this study we compare the effect of Jacobson relaxation technique and Pranayama technique on the SOB, Cough, sputum and quality of life in COPD patients. Data were collected from Gulab Devi Chest Hospital, General Hospital, Jinnah Hospital and Mayo Hospital Lahore. Data were collected by the lottery method. Borg dyspnea scale, Spirometry, CASA-Q and Quality of life questionnaire were used before and after the intervention. Treatment was continuous 4 weeks, 3 times in a week for 15 mint. Assessment was done through the tool before and after the treatment.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date December 10, 2023
Est. primary completion date December 1, 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria: - • Patients of Age between 40 and 70. - Both Genders (Male, Female) were included. - Stage 2 patient with COPD with Dyspnea FEV1 <70% and Maximal Expiratory Pressure = 50% (Gold Criteria) were included. - Cognitive Stable patients were included. - Those Patients were included who were clinically stable without exacerbations in the past 01 month. Exclusion Criteria: - • Common Cough - Upper respiratory tract inflammation - Patients who have other co-morbid diseases which prevents them from exercise training, for example, disability due to neurological, orthopedic and acute cardiac causes - Patients who were mentally and physically and sick to join at the hospital or research site for training - Patients who were already participated or completed or in a P.R program in the past one year.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Jacobsons Breathing Technique
Quality of life, cough and sputum analysis, spirometry, and shortness of breath were assessed.
Pranayama Technique
Quality of life, cough and sputum analysis, spirometry, and shortness of breath were assessed.

Locations

Country Name City State
Pakistan Gulab Devi Chest Hospital Lahore Punjab

Sponsors (1)

Lead Sponsor Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

References & Publications (5)

Basoglu OK, Atasever A, Bacakoglu F. The efficacy of incentive spirometry in patients with COPD. Respirology. 2005 Jun;10(3):349-53. doi: 10.1111/j.1440-1843.2005.00716.x. — View Citation

Ozgundondu B, Gok Metin Z. Effects of progressive muscle relaxation combined with music on stress, fatigue, and coping styles among intensive care nurses. Intensive Crit Care Nurs. 2019 Oct;54:54-63. doi: 10.1016/j.iccn.2019.07.007. Epub 2019 Jul 29. — View Citation

Pauwels RA, Buist AS, Ma P, Jenkins CR, Hurd SS; GOLD Scientific Committee. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: National Heart, Lung, and Blood Institute and World Health Organization Global Initiative for Chronic Obstructive Lung Disease (GOLD): executive summary. Respir Care. 2001 Aug;46(8):798-825. No abstract available. — View Citation

Petty TL. The history of COPD. Int J Chron Obstruct Pulmon Dis. 2006;1(1):3-14. doi: 10.2147/copd.2006.1.1.3. — View Citation

Ranjita R, Hankey A, Nagendra HR, Mohanty S. Yoga-based pulmonary rehabilitation for the management of dyspnea in coal miners with chronic obstructive pulmonary disease: A randomized controlled trial. J Ayurveda Integr Med. 2016 Jul-Sep;7(3):158-166. doi: 10.1016/j.jaim.2015.12.001. Epub 2016 Aug 18. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Dyspnea Severity (Borg Scale) The Borg scale measures the severity of dyspnea (shortness of breath).
Scale Details:
Full Title: Borg Rating of Perceived Exertion (RPE) ScaleFull Title: Borg Rating of Perceived Exertion (RPE) Scale Minimum Value: 0 (No breathlessness at all) Maximum Value: 10 (Maximal breathlessness) Interpretation: Higher scores indicate worse outcomes, meaning greater severity of dyspnea.
4 weeks
Primary Cough and Sputum Analysis (CASA-Q) The CASA-Q (Cough and Sputum Assessment Questionnaire) evaluates the severity and impact of cough and sputum production.
Scale Details:
Full Title: Cough and Sputum Assessment Questionnaire (CASA-Q) Minimum Value: 0 (No symptoms) Maximum Value: 100 (Severe symptoms) Interpretation: Higher scores indicate worse outcomes, meaning more severe symptoms of cough and sputum.
4 Weeks
Primary Spirometry (FEV1 and FVC) Spirometry will be used to measure lung function, specifically Forced Expiratory Volume in 1 second (FEV1) and Forced Vital Capacity (FVC).
Scale Details:
Full Title: Spirometry (FEV1 and FVC) Minimum Value: Variable (dependent on patient's lung function) Maximum Value: Variable (dependent on patient's lung function) Interpretation: Higher values typically indicate better lung function.
4 Weeks
Secondary Quality of Life (SF-36 Questionnaire) The SF-36 (Short Form Health Survey) questionnaire assesses the overall quality of life.
Scale Details:
Full Title: SF-36 Health Survey Minimum Value: 0 (Worst possible health state) Maximum Value: 100 (Best possible health state) Interpretation: Higher scores indicate better quality of life.
4 Weeks
Secondary Patient Satisfaction (Patient Satisfaction Questionnaire) The Patient Satisfaction Questionnaire measures the satisfaction of patients with the treatment they received.
Full Title: Patient Satisfaction Questionnaire (PSQ) Minimum Value: 1 (Very dissatisfied) Maximum Value: 5 (Very satisfied) Interpretation: Higher scores indicate greater satisfaction.
4 Weeks
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