- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06995989
- Original Trial
Effects of Energy Conservation Techniques With Pursed Lip Breathing on Quality of Life in Bronchiectasis
Combined Effects of Energy Conservation Techniques With Pursed Lip Breathing on Functional Independence and Quality of Life in Bronchiectasis
Bronchiectasis is the abnormal dilatation of the bronchi. Due to airway dilatation patient is unable to clear the mucus and risk of infection is increased. For mucus clearance used many breathing techniques employed along with or without mechanical devices. Many researches have shown the inconsistent results of energy conservation techniques along with breathing exercises among variety of cardiopulmonary disorders. This study will be conducted to determine the combined effects of energy conservation techniques with pursed lip breathing on functional independence and quality of life in patients of bronchiectasis. It will be a randomized clinical trial. Two groups will be taken under the age of 40 to 60 years and data will be collected from pulmonary wards of selected hospitals. Sample size will be 46 keeping the attrition rate 10%.
St. George's Respiratory Questionnaire (SGRQ) will be used to evaluate the quality of life of patients and 6 mint walk test is used to determine functional independence of bronchiectasis patients. After data collection, data will be analyzed using SPSS version 26.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Imran Amjad, PhD
- Phone Number: 03324390125
- Email: imran.amjad@riphah.edu.pk
Study Locations
-
-
Punjab
-
Sargodha, Punjab, Pakistan, 40100
- Sadiq hospital Sargodha, DHQ Sargodha
-
Contact:
- Arjumand Bano, MS-CPPT
- Phone Number: 03059551883
- Email: arjumand.bano@riphah.edu.pk
-
Principal Investigator:
- Faria Iftikhar, MS-CPPT
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Both genders, aged between 40 to 60 years Bronchiectasis
Exclusion Criteria:
Prior history of open-heart surgery
- Prior severe pulmonary/hepatic or renal disease
- Life-threatening arrhythmias (ventricular fibrillation, ventricular tachycardia, atrial fibrillation)
- Pulmonary complications (atelectasis, acute respiratory distress syndrome (ARDS), diaphragmatic injury)
- Congestive heart failure
- Deep venous thrombosis (DVT)
- Any known psychological disease
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: energy conservation techniques along with pursed lip breathing technique
Group A will receive energy conservation techniques with pursed lip breathing with 1 session a day for total 5 days in a week. 1 session will consist of 3 cycles of pursed lip breathing for duration of 10 minutes with a break of 20 minutes in between. ECTs will be trained for 2 weeks. A detailed manual will be developed to ensure the consistency of the training for all subjects. Examples of interventions are training to use ergonomic principles along with pursed lip breathing. The subjects were trained to place their equipment at chest height; they were trained to work at paced speed and in some cases instructed to use technical aids. |
Group A will receive energy conservation techniques with pursed lip breathing with 1 session a day for total 5 days in a week. 1 session will consist of 3 cycles of pursed lip breathing for duration of 10 minutes with a break of 20 minutes in between. ECTs will be trained for 2 weeks. A detailed manual will be developed to ensure the consistency of the training for all subjects. Examples of interventions are training to use ergonomic principles along with pursed lip breathing. The subjects were trained to place their equipment at chest height; they were trained to work at paced speed and in some cases instructed to use technical aids. |
|
Experimental: pursed lip breathing technique
Group B will receive pursed lip breathing
|
pursed lip breathing
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
St. George's Respiratory Questionnaire (SGRQ)
Time Frame: 2 weeks
|
Patients completed on paper the SGRQ, it includes dimensions for SGRQ activity, SGRQ impact, SGRQ symptoms, and SGRQ total.
The scale ranges from 0 (excellent quality of life) to 100 (worst quality of life) for all four dimensions
|
2 weeks
|
|
6 Minutes walk test
Time Frame: 2 weeks
|
The patient is asked to walk as far as possible along a 30-m minimally trafficked corridor for a period of 6 min with the primary outcome measure being the 6-min walk distance (6MWD) measured in meters
|
2 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Arjumand Bano, MS-CPPT, Riphah International University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
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/24/0358
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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