- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06459843
Effects Of of Pursed Lip Breathing and Coordinated Breathing in Adult Patients With COPD
January 10, 2025 updated by: Riphah International University
Combined Effects Of of Pursed Lip Breathing and Coordinated Breathing During Aerobic Exercise on Aerobic Capacity, Dyspnea and Anxiety Level in Adult Patients With COPD
COPD is the chronic lung condition characterized by the damage and enlargement of the air sacs in the lungs, leading to breathing difficulties.
A blockage may develop, which traps air inside your lungs.
The patient shows clinical manifestation of cough, wheezing, chest tightness, shortness of breath.
This research of randomized clinical trial will check the combined effects of pursed lip breathing and coordinated breathing techniques to improve aerobic capacity and dyspnea in patients with COPD by taking sample of 54 patients through convenience sampling and randomly allocating them to two groups A and B out of which A will receive pursed lip breathing with aerobic exercise for 4 times per week for 4 week and duration will be 45-60 min, B will receive coordinated breathing with aerobic exercise for 4 times per week for 4 weeks.
And duration will be 45-60 min.Pre and post training outcomes of aerobic capacity and dyspnea will be measured through Six minute walk test and dyspnea Borg scale, and Saint George respiratory questionnaire.
The data will be analyzed through SPSS 21.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
54
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan, 54000
- Jinnah Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Age range 25 -45 years(5)
- Adult patient diagnosed with (chronic obstructive pulmonary disease) based on clinical and diagnostic criteria.
- Patient willing and able to participate in an pursed lip breathing and coordinated breathing exercise program
- Gender both male and female
Exclusion Criteria:
- Those who cognitive impairment that might affect their ability to comprehend and follow instructions
- Any contraindication to the use of pursed lip breathing or coordinated breathing exercise as determined by the health care provider.
- Individual with severe musculoskeletal limitations or other physical condition that may hinder the ability to perform exercise
- Individual who have experienced the recent exacerbation of COPD symptoms within past three month
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
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: pursed lip breathing techniques
Pursed lip breathing with aerobic exercise for 4 times per week for 4 week and duration will be 45-60 min.
Relax your neck and shoulder muscles.
For the use of PLB exercise, the intervention will be given every day till the patient discharged from hospital.
Patient will perform 5 sets
|
Relax your neck and shoulder muscles.
For the use of PLB exercise, the intervention will be given every day till the patient discharged from hospital.
Patient will perform 5 sets.
In each set, 10 times will be included.
Then, instruct the patient to take deep breath through nose for two counts, and keep mouth closed.
Inhale for 2 seconds.
Now, ask the patient to purse the lips as if the patient was going to gently flicker the flame of candle.
Now the patient will breathe out gently while counting for 4 seconds.
|
|
Active Comparator: coordinated breathing technique
The intervention will be given un every day till the patient discharge from hospital.
Coordinated breathing with aerobic exercise for 4 times per week for 4 weeks.
And duration will be 45-60 min
|
Put one hand on your abdomen.
Make your abdomen push out while you breathe in through your nose.
Suck in your abdominal muscles.
Breathe out using the pursed-lip technique.
You should feel your abdomen go down.
Repeat three times and rest for two minutes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Six minute walk test
Time Frame: baseline and fourth week
|
Patients were instructed to walk back and forth at their own pace in a 35 m corridor.
A physiotherapist supervised the test through the course, telling the patient the remaining exercise time every 2 min
|
baseline and fourth week
|
|
Borg dyspnea scale
Time Frame: baseline and fourth week
|
Dyspnea during the test was evaluated with the modified Borg dyspnea score.
Pulmonary function test, inspiratory capacity, and dyspnea score, together with the walking distance were recorded before and after walking.
Modified Borg scale is valid patient self-report scale for measuring breathlessness after exercise with the scaling from 0 to 10.
|
baseline and fourth week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Sidra Afzal, PP-DPT, Riphah International University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Thurlbeck WM, Muller NL. Emphysema: definition, imaging, and quantification. AJR Am J Roentgenol. 1994 Nov;163(5):1017-25. doi: 10.2214/ajr.163.5.7976869.
- Rodrigues A, Munoz Castro G, Jacome C, Langer D, Parry SM, Burtin C. Current developments and future directions in respiratory physiotherapy. Eur Respir Rev. 2020 Dec 15;29(158):200264. doi: 10.1183/16000617.0264-2020. Print 2020 Dec 31.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 15, 2024
Primary Completion (Actual)
July 15, 2024
Study Completion (Actual)
July 15, 2024
Study Registration Dates
First Submitted
June 11, 2024
First Submitted That Met QC Criteria
June 11, 2024
First Posted (Actual)
June 14, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 10, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR & AHS/23/0366
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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