- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05591729
Effect of Pilates on Balance and Spinal Curvature In Upper Crossed Syndrome (UCS)
February 15, 2023 updated by: Mariam omran Grase, Cairo University
The study will be conducted to investigate the effect of Pilates exercise on spinal curvature and balance in patients with the upper cross syndrome. .
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Upper crossed syndrome (UCS) is the most common postural dysfunction in the musculature of the shoulder girdle /cervicothoracic region, which creates joint dysfunction, particularly at the atlanto-occipital joint, cervicothoracic joint C4-C5 segment, glenohumeral joint and T4-T5 segment.
Pilates is designed as a program that will work with other exercise programs to strengthen, rebalance and realign the body.
Pilates trains individuals to identify their own musculoskeletal strengths and weaknesses and equips them with the knowledge to correct and rebalance their entire body mechanics (Worth,2004) thus, the focus is also placed on improving personal body awareness which further decreases the risks of strain or injury that can occur with imbalances.
forty patients with UCS will be allocated randomly into two groups; one experimental group will receive pilates exercise and postural correction twice a week for four weeks, and the control group will receive postural correction exercise along twice a week for four weeks
Study Type
Interventional
Enrollment (Actual)
40
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 Contact
- Name: mariam O gras, lecturer
- Phone Number: 01005541018
- Email: Dr.mariamomran@yahoo.com
Study Locations
-
-
-
Giza, Egypt
- Faculty of physical therapy Cairo
-
-
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
17 years to 22 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- The patient's age ranged from 17 to 22 years
- Body mass index between 20-25 kg/m2
- The participants are diagnosed with upper cross syndrome
- Patients with normal cognitive aspects willing and able to participate in a program safely
Exclusion Criteria:
- The participants have experienced any recent trauma (within 3 months of the initial consultation)
- The participant's primary complaint is that of headaches or facial pain.
- Contra-indications to pilates are found pregnancy, hypertension, osteoporosis, and spinal tumors.
- Participants have any sort of structural abnormality in upper and middle back e.g., Scoliosis, or had a positive Adams test.
- Participants who are taking anti-inflammatory or muscle relaxant medication had to have a three-day "wash out" period before participating in the study
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Pilates exercise
pilates exercise will be received twice a week for four weeks
|
Each Pilates session will last for one hour.
The subjects will be taught the 5 key elements of Pilates (lateral costal breathing, centering which is a neutral position of the lumbar spine with activation of the core muscles, ribcage placement, shoulder blade placement and neutral position of the cervical spine with slight upper cervical flexion at the craniocervical junction).
A pilates exercise program will consist of 11 levels of treatment program.
the patients will receive postural correction exercises, stretches, and exercises to the pectoralis major, elevator scapulae, upper trapezius, serratus anterior, rhomboids, and deep neck flexors.
The stretches included sitting chair stretches, Brugger's, wall angels, and doorway stretches.
The exercises included push-up-plus, head-neck-retraction, and Kibler squeeze
|
Active Comparator: postural correction exercise
postural correction exercises will be received twice a week for four weeks
|
the patients will receive postural correction exercises, stretches, and exercises to the pectoralis major, elevator scapulae, upper trapezius, serratus anterior, rhomboids, and deep neck flexors.
The stretches included sitting chair stretches, Brugger's, wall angels, and doorway stretches.
The exercises included push-up-plus, head-neck-retraction, and Kibler squeeze
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
spinal curvature
Time Frame: up to four weeks
|
spinal mouse will be used to assess thoracic spine curvature.
Total angle of the thoracic spine is 41-44 degree.
|
up to four weeks
|
balance
Time Frame: up to four weeks
|
balance will be measured by Biodex balance system
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up to four weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
craniovertebral angle
Time Frame: up to four weeks
|
craniovertebral angle will be measured by photogrammetric method
|
up to four weeks
|
shoulder posture
Time Frame: up to four weeks
|
The shoulder's rounded position will be measured by tap measurement.
the patients will be in supine and the therapist measure the distance from their shoulder to the plinth using tape measurements.
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up to four weeks
|
pain intensity
Time Frame: up to four weeks
|
pain will be measured by visual analogue scale
|
up to four weeks
|
neck function
Time Frame: up to four weeks
|
neck function will be measured by Arabic neck disability index..
It consisting of 10 items with six choices.
There is no disability for scores from 0 to 4; 5-14 is mild; 15-24 is moderate; 25-34 is severe, and finally more than 34 is a complete disability.
|
up to four weeks
|
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 25, 2022
Primary Completion (Actual)
December 1, 2022
Study Completion (Actual)
December 1, 2022
Study Registration Dates
First Submitted
October 19, 2022
First Submitted That Met QC Criteria
October 19, 2022
First Posted (Actual)
October 24, 2022
Study Record Updates
Last Update Posted (Estimate)
February 16, 2023
Last Update Submitted That Met QC Criteria
February 15, 2023
Last Verified
February 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T/012/003992
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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