- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06479902
Effects of Core Stability Combined With Diaphragmatic Strengthening Exercises Among Asthmatic Patients
June 26, 2024 updated by: Foundation University Islamabad
This is a quasi intervention study evaluating the effects of core stabilization exercises and diaphragmatic strengthening on thoracic kyphosis angle, diaphragmatic excursion, chest expansion, lung functioning (FEV1/FVC ratio) and quality of life, in individuals with mild intermittent or mild persistent asthma.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study evaluated the effects of core stabilization exercises and diaphragmatic strengthening on thoracic kyphosis angle, diaphragmatic excursion, chest expansion, lung functioning (FEV1/FVC ratio), and quality of life in individuals with mild intermittent or mild persistent asthma.
Thirty-seven participants from Fauji Foundation Hospital Rawalpindi underwent assessments before and after an 18-session treatment regimen over three weeks.
The measures included diaphragmatic excursion, thoracic kyphotic angle, chest expansion, spirometry, and asthma quality of life questionnaire.
Statistical analysis was performed using SPSS version 21
Study Type
Interventional
Enrollment (Actual)
41
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
-
Rawalpindi, Punjab, Pakistan, 46000
- Foundation University College of Physical Therapy
-
-
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
No
Description
Inclusion Criteria:
- Age group: 18-34 years old
- Both males and females
- Individuals diagnosed with well controlled mild intermittent asthma or mild persistent asthma, at least six months prior based on referral from pulmonologist.
- Individuals who have weak core muscles
- Participating to the study in a voluntary basis
Exclusion Criteria:
- Level 3 and above asthmatics or status asthmaticus
- Any congenital deformities of chest wall
- Demonstrated neuromuscular or neurological deficit/disease of chest wall.
- Cardiopulmonary diseases including coronary artery disease, heart failure NYHA classification, valvular heart disease, cardiomyopathy, arrythmias, interstitial lung disease, COPD, pulmonary embolism, pulmonary hypertension, cancers, etc.
- Any recent cardiothoracic or abdominal surgery or sternotomy
- Recent history of the blunt chest wall or abdominal trauma
- Unstable hemodynamic parameters (arterial pressure >140mmhg systolic and >90mmhg for diastolic
- Pregnancy
- Previous or parallel participation in interventional programs
- Any psychiatric illnesses
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: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Core stabilization and Diaphragmatic Exercise Group
The intervention consisted of 18 sessions over three weeks, following the FITT protocol.
Each session included a warm-up (5 minutes), core stability exercises (15 minutes), diaphragmatic strengthening exercises (10 minutes), and cool-down (5 minutes), with rest intervals.
Exercises progressed in difficulty on stable surfaces, tailored to each participant's tolerance.
Warm-up exercises included activities like hopping and knee circles, while core stability exercises featured moves such as planks and side planks.
Diaphragmatic exercises included diaphragmatic breathing in various positions.
|
Core stability exercises featured moves such as planks and side planks.
. Diaphragmatic exercises included diaphragmatic breathing in various positions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Thoracic Kyphosis Angle
Time Frame: 18 days
|
Measured with Inclinometer
|
18 days
|
|
Diaphragmatic Excursion
Time Frame: 18 days
|
Measured using Tape method
|
18 days
|
|
Chest Expansion
Time Frame: 18 days
|
Measured using Tape method
|
18 days
|
|
FEV1/FVC ratio
Time Frame: 18 days
|
Measured using Spirometer
|
18 days
|
|
Quality of Life of patient
Time Frame: 18 days
|
Asthma Quality of Life Questionnaire with Standardized Activities.
It is a 32-item Likert-type scale that measures the impact of asthma on daily activities, with scores ranging from 1 (severe impairment) to 7 (no impairment).
|
18 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
July 15, 2023
Primary Completion (Actual)
April 18, 2024
Study Completion (Actual)
May 24, 2024
Study Registration Dates
First Submitted
June 7, 2024
First Submitted That Met QC Criteria
June 26, 2024
First Posted (Actual)
June 28, 2024
Study Record Updates
Last Update Posted (Actual)
June 28, 2024
Last Update Submitted That Met QC Criteria
June 26, 2024
Last Verified
June 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FUI/CTR/2024/14
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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