- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04773860
Muscle Energy Techniques in COPD Patients
Muscle Energy Techniques in Chronic Obstructive Disease Patients: Effects on Pulmonary Function and Activities of Daily Living
Patients diagnosed with COPD as a result of hyperinflation adapt to the increased workload through shortening and overactivation of other muscles because of their dual function as muscles of the upper limb and neck motion which makes them limited in function and decreases the range of motion in these joints. Another resultant effect of these changes is the shortness of breath taking place following the inability of patients to perform daily activities.
Current research is focusing on the use of Muscle Energy Techniques (METs) for such circumstances. Therefore, this study aims to evaluate whether METs result in an improvement in rib cage mobility which could potentially lead to improvements in pulmonary function and activities of daily of living (ADLs) in a group of patients diagnosed with COPD. If positive results are obtained, such an intervention might provide a possible addition to the evidence-based interventions already available for COPD patients. The result of this intervention may provide physiotherapists with further techniques for use in such patients; ones which will be of benefit to the patients and their quality of life and also to the health services.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Patients diagnosed with COPD as a result of hyperinflation adapt to the increased workload through shortening and overactivation of other muscles because of their dual function as muscles of the upper limb and neck motion which makes them limited in function and decreases the range of motion in these joints. Another resultant effect of these changes is the shortness of breath taking place following the inability of patients to perform daily activities.
Current research is focusing on the use of Muscle Energy Techniques (METs) for such circumstances. Therefore, this study aims to evaluate whether METs result in an improvement in rib cage mobility which could potentially lead to improvements in pulmonary function and activities of daily of living (ADLs) in a group of patients diagnosed with COPD. If positive results are obtained, such an intervention might provide a possible addition to the evidence-based interventions already available for COPD patients. The result of this intervention may provide physiotherapists with further techniques for use in such patients; ones which will be of benefit to the patients and their quality of life and also to the health services.
A randomised controlled trial (RCT) shall be carried out on an approximate sample of 110 patients diagnosed with COPD. Participants shall be randomly assigned to an intervention and a control group. The intervention group shall be receiving a 4 week programme of Muscle Energy Techniques whereas the control group shall continue with their prescribed medications and any conventional physiotherapy sessions suggested for these patients.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Kimberley Sevasta, BSc
- Phone Number: 356 79980164
- Email: sevastakimberley@gmail.com
Study Contact Backup
- Name: Anabel Sciriha, PhD
- Phone Number: 356 99423327
- Email: anabel.sciriha@um.edu.mt
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- The patient has to have been diagnosed as suffering from COPD by a medical consultant,
- Be medically stable with no exacerbations within the past 2 months and,
- Be between the age range of 40 to 79 years of age.
Exclusion Criteria:
- Rheumatoid arthritis,
- Musculoskeletal or neuromuscular pathology and,
- Cognitive disability that could affect comprehension or execution of the intervention protocol or outcome measurements
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: Experimental
The experimental group shall be receiving a 4 week programme of Muscle Energy Techniques on the following accessory muscles; Sternocleidomastoid, Pectoralis Minor, Trapezius, Scalene muscles and Latissimus Dorsi
|
A 4 week intervention will be carried out consisting of Muscle Energy Techniques on the accessory muscle of respiration.
That is, Pectoralis Minor, Sternocleidomastoid, Upper trapezius, Scalene muscles and Latissimus Dorsi
|
No Intervention: Control group
The control group will be taking their prescribed medication and continue with any conventional physiotherapy recommended for the individual.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Lung function test
Time Frame: Week 0, Week 4 and Week 8
|
Spirometry
|
Week 0, Week 4 and Week 8
|
Change in Chest expansion
Time Frame: Week 0, Week 4 and Week 8
|
Chest expansion using a tape measure
|
Week 0, Week 4 and Week 8
|
Change in 6 Minute Walk Test
Time Frame: Week 0, Week 4 and Week 8
|
An endurance test over a 6 minute time frame using a 30m course
|
Week 0, Week 4 and Week 8
|
Change in Manchester Related Activities of Daily Living Questionnaire
Time Frame: Week 0, Week 4 and Week 8
|
MR-ADL is a reliable physical disability scale.
It is a self-completed scale and usually takes around 10 minutes to complete.
It assesses functional ability in 4 different domains, that is in the kitchen, mobility, domestic tasks and leisure activities
|
Week 0, Week 4 and Week 8
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
- 333797
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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