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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05591729
Other study ID # P.T/012/003992
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 25, 2022
Est. completion date December 1, 2022

Study information

Verified date February 2023
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study will be conducted to investigate the effect of Pilates exercise on spinal curvature and balance in patients with the upper cross syndrome. .


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


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date December 1, 2022
Est. primary completion date December 1, 2022
Accepts healthy volunteers No
Gender All
Age group 17 Years to 22 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Pilates exercises
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.
postural correction exercise
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

Locations

Country Name City State
Egypt Faculty of physical therapy Cairo Giza

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary spinal curvature spinal mouse will be used to assess thoracic spine curvature. Total angle of the thoracic spine is 41-44 degree. up to four weeks
Primary balance balance will be measured by Biodex balance system up to four weeks
Secondary craniovertebral angle craniovertebral angle will be measured by photogrammetric method up to four weeks
Secondary pain intensity pain will be measured by visual analogue scale up to four weeks
Secondary neck function 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
Secondary shoulder posture 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. up to four weeks
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