- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06480422
Combined Effects Of Autogenic Drainage and Segmental Breathing Techniques in Chronic Obstructive Pulmonary Disease
Study Overview
Status
Conditions
Intervention / Treatment
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 Contact Backup
- Name: Iqbal Tariq, phd
- Phone Number: 03338236752
- Email: Iqbal.tariq@riphah.edu.pk
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan, 54000
- Recruiting
- Ever Care Hospital
-
Contact:
- Sidra Afzal, PP-DPT
- Phone Number: 03124378540
- Email: sidra.afzal@riphah.edu.pk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age between 40 - 60 years.
- Diagnosed moderate COPD patients according to GOLD criteria.
- FEV / FVC ratio < 70 years
- Stable patients can understand written and oral english,urdu trial information.
Exclusion Criteria:
- Pregnancy, due to the Pressure on pelvic and Abdomen muscles.
- Malignant disease
- Severe (RA)
- Diagnosis of Asthma and major diseases, functionally limiting diseases, life expectancy < 3 months.
- Neurological disorders
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 |
|---|---|
|
Experimental: segmental breathing technique + Autogenic drainage
For Segmental Breathing instruction, the therapist's hand is placed on the chest area to be expanded.
The patient is encouraged to deeply breath and to preferentially "Send Air"to that area of chest where tactile stimulation is being applied by the therapist.
On full expiration moderate compression is applied.
To begin an autogenic drainage sit in a relaxed seated position with neck extended slightly.
Blow patient's nose and huff, cough to clear your upper airways to mucus.
This technique has three phases.
Moving mucus from small airways (Unsticking), Moving mucus from small airways to medium sized airways(Collecting), Moving mucus from medium sized airways to large airways (Evacuation) Take in a deep breath.
Hold the breath for three seconds.
With some gentle force exhale all the air out of your lungs.
Repeat three times.
Do not cough untill after the third breath.
Repeat sessions 3 times in a week for 4 almost weeks.
|
To begin an autogenic drainage sit in a relaxed seated position with neck extended slightly.
Blow patient's nose and huff, cough to clear your upper airways to mucus.
This technique has three phases.
Moving mucus from small airways (Unsticking), Moving mucus from small airways to medium sized airways(Collecting), Moving mucus from medium sized airways to large airways(Evacuation) Take in a deep breath.
Hold the breath for three seconds.
With some gentle force exhale all the air out of your lungs.
Repeat three times.
Do not cough untill after the third breath.
Repeat sessions 3 times in a week for 4 almost weeks.
Repeat the cycle untill you have cleared your lungs as much as possible, 20 and 45 minutes.
Other Names:
To begin an autogenic drainage sit in a relaxed seated position with neck extended slightly.Blow ptient's nose and huff, cough to clear your upper airways to mucus.This technique has three phases. Moving mucus from small airways (Unsticking), Moving mucus from small airways to medium sized airways(Collecting), Moving mucus from medium sized airways to large airways(Evacuation) Take in a deep breath.Hold the breath for three seconds.With some gentle force exhale all the air out of your lungs. Repeat three times.Do not cough untill after the third breath. Repeat sessions 3 times in a week for 4 almost weeks. Repeat the cycle untill you have cleared your lungs as much as possible, which should take between 20 and 45 minutes. |
|
Active Comparator: Autogenic drainage
To begin an autogenic drainage sit in a relaxed seated position with neck extended slightly. Blow ptient's nose and huff, cough to clear your upper airways to mucus.This technique has three phases. Moving mucus from small airways (Unsticking), Moving mucus from small airways to medium sized airways(Collecting), Moving mucus from medium sized airways to large airways(Evacuation) Take in a deep breath.Hold the breath for three seconds.With some gentle force exhale all the air out of your lungs. Repeat three times.Do not cough untill after the third breath. Repeat sessions 3 times in a week for 4 almost weeks. |
To begin an autogenic drainage sit in a relaxed seated position with neck extended slightly.Blow ptient's nose and huff, cough to clear your upper airways to mucus.This technique has three phases. Moving mucus from small airways (Unsticking), Moving mucus from small airways to medium sized airways(Collecting), Moving mucus from medium sized airways to large airways(Evacuation) Take in a deep breath.Hold the breath for three seconds.With some gentle force exhale all the air out of your lungs. Repeat three times.Do not cough untill after the third breath. Repeat sessions 3 times in a week for 4 almost weeks. Repeat the cycle untill you have cleared your lungs as much as possible, which should take between 20 and 45 minutes. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
SPIROMETER
Time Frame: baseline and fourth week
|
The most used pulmonary function test is spirometry.
It assesses the capacity of the lungs to breathe in and out, especially the volume and/or velocity of air that can be expelled.
When evaluating breathing patterns to detect diseases including asthma, pulmonary fibrosis, cystic fibrosis, and COPD, spirometry is useful.
An FEV1/FVC ratio larger than 0.70 with both FEV1 and FVC over 80% of the expected value are considered normal spirometry data.
TLC exceeding 80% of the predicted value is typical in the event that lung volumes are measured.
Diffusion capacity that is more than 75% of the expected value is likewise regarded as typical
|
baseline and fourth week
|
|
PULSE OXIMETER
Time Frame: baseline and fourth week
|
Pulse oximetry operates by shining a light through the skin at two different wavelengths_660 nm(red) and 940nm(infrared)_ and measuring the difference in light absorbance at the two wavelengths to estimate an arterial oxygen saturation
|
baseline and fourth week
|
|
BREATHLESSNESS COUGH SPUTUM SCALE(BCSS)
Time Frame: baseline and fourth week
|
The breathlessness cough sputum scale tool is an effective means for measuring the impact of Pulmonary rehabilitation on improving patient tolerance and self reported symptoms as the result of COPD
|
baseline and fourth week
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sidra Afzal, PP-DPT, Riphah International University
Publications and helpful links
General Publications
- Fink JB. Forced expiratory technique, directed cough, and autogenic drainage. Respir Care. 2007 Sep;52(9):1210-21; discussion 1221-3.
- Ali RA, Obeisat SM, Tarawneh LH. Improving nursing knowledge and care for neonates with respiratory distress in Jordan. Int Nurs Rev. 2019 Sep;66(3):338-345. doi: 10.1111/inr.12510. Epub 2019 Apr 1.
- Zak M, Gauchez H, Boberski M, Stangret A, Kempinska-Podhorodecka A. Effectiveness of Autogenic Drainage in Improving Pulmonary Function in Patients with Cystic Fibrosis. Int J Environ Res Public Health. 2023 Feb 21;20(5):3822. doi: 10.3390/ijerph20053822.
Study record dates
Study Major Dates
Study Start (Actual)
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/23/0381
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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