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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04775251
Other study ID # P.T.REC/012/002640
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date February 28, 2021
Est. completion date August 2021

Study information

Verified date February 2021
Source Cairo University
Contact Doha Al-Afifi
Phone 01003169353
Email doha.h.afifi@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It was hypothesized that: There is no statistical significant effects of a scapular vupward rotation exercise (SURE) on scapular alignment in subjects with scapular downward rotation syndrome (SDRS). There is no statistical significant effects a scapular upward rotation exercise (SURE) on mechanosensitivity of the upper limb peripheral nervous system in a depressed scapular alignment subjects. There is no statistical significant effects a scapular upward rotation exercise (SURE) on pressure Pain Threshold in a depressed scapular alignment subjects. There is no statistical significant effects a scapular upward rotation exercise (SURE)on Strenght Duration Curve measurement in a depressed scapular alignment subjects.


Description:

This study was conducted to investigate the effects of scapular upward rotation exercises on strength duration curve and pressure pain threshold (PPT) in subjects with scapular downward rotation syndrome. Thirty subjects with age range of 18 to 30 years with scapular downward rotation were recruited in this study. Thirty subjects of both gender with scapular downward rotation were recruited in this study. All recruited subjects were examined to exclude defined pathological conditions. All subjects were assessed by screening examination for downward rotation of scapula. Pressure pain threshold was measured using pressure algometer. Mechanosensitivity of neural tissue was measured using neurodynamic test. Pain was measured using strength-duration (SD) curve. Treatment program consisted of 3 sessions/week, for 6 weeks. All measurements were taken pre and post the treatment period.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date August 2021
Est. primary completion date May 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - University population were screened for subjects with scapular downward rotation, those who met the following criteria was recruited in this study. The inclusion criteria for subject selection in this study was based on the literature (Caldwell et al., 2007; Ha et al., 2011) which included: 1. The scapula was downwardly rotated by visual appraisal.We examined the root of spine of scapulae (superior angle) and inferior angle of scapulae. If scapulae was downwardly rotated, inferior angle closer to spine than root of spine of scapulae (superior angle). 2. The clavicle appeared to be horizontal or the acromioclavicular joint was lower than the sternoclavicular joint by visual appraisal. 3. The vertebral borders of the scapula was less than 3 inches from the spine by tape measure. Exclusion Criteria: - Subject who has any of the following criteria was excluded from the study: 1. Subjects with cervical spinal fractures. 2. Neck-rotation ROM of <20ยบ. 3. Radiating pain to an upper extremity. 4. Scoliosis. 5. Leg length discrepancy. 6. A history of unresolved cancer. 7. Diabetes Miletus. 8. Polyneuropathy. 9. Myofascial Pain Syndrome. 10. Fibromyalgia.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Upward rotation exercise
Treatment for correction of depressed scapular Alignment by exercise ( Upward Rotation Exercises) for 6 weeks.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary Neural excitability Neural excitability measured by Strenght-duration cruve. Strenght-duration curve for neural excitability is measured before starting the treatment.Strenght-duration is measured after application of 6 weeks treatment program.
Secondary Pressure pain threshold Pressure pain threshold was measured using pressure algometer. All measurements were taken pre and post the treatment period (6 weeks).
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