- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05894304
The Effects of Scapular Muscles Training Using a Suspension System in Patients With Non Spacific Chronic Neck Pain and Scapular Dyskinesia
June 8, 2023 updated by: Nourhan Gamal Khattab, Cairo University
The study aimed to investigate the effect of scapular muscle training using a suspension system in patients with non spacific chronic neck pain with scapular diskinesia
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
52
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
-
-
-
Giza, Egypt
- Cairo University
-
-
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:
- Patients age between 20-35 years.
- Patients with non spacific pain(pain > 3 month).
- pain must have been present for at least the previous 12 weeks.
- Patients with non spacific chronic neck pain with scapular dyskinesia.
- Patient BMI<30.
Exclusion Criteria:
- History of previous neck surgery.
- Recent or old fractures.
- Cognitive impairment and inability to understand the scale.
- Systematic inflammatory disease e.g., rheumatoid arthritis and ankylosing Spondylitis.
- Neck pain with radiculopathy or neuropathy.
- Scapular dyskinesia due to other pathology such as shoulder impingement
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Excercise therapy group
The group that recived scapular muscle training exercises
|
Scapular muscle strength by resistance
|
|
Experimental: Suspension group
The group that recived scapular muscle training using suspension system
|
suspended from the handles of the straps by either their hands or feet while the non-suspended pair of extremities are in contact with the ground leading to muscle activation due to unstable base of support
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Scapular muscle strength
Time Frame: 1week
|
Scapular muscle strength is measured by hand held dynanometer
|
1week
|
|
Scapular position
Time Frame: 1week
|
Scapular position is measured by lateral scapular slide test
|
1week
|
|
Pain intensity
Time Frame: 1week
|
Pain intensity is measured by neumeric pain rating scale the lowest value is 0 means no pain and the highest value is 10 means the worst pain
|
1week
|
|
Function
Time Frame: 1 week
|
Function is measured by neck disability index the total score is 50 as the score is higher the disability is higher
|
1 week
|
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)
October 1, 2022
Primary Completion (Actual)
May 30, 2023
Study Completion (Actual)
May 30, 2023
Study Registration Dates
First Submitted
May 30, 2023
First Submitted That Met QC Criteria
May 30, 2023
First Posted (Actual)
June 8, 2023
Study Record Updates
Last Update Posted (Actual)
June 12, 2023
Last Update Submitted That Met QC Criteria
June 8, 2023
Last Verified
June 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/004031
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
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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