NCT04775251

Brief 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.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2021

Shorter than P25 for not_applicable

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 6, 2021

Completed
22 days until next milestone

Study Start

First participant enrolled

February 28, 2021

Completed
1 day until next milestone

First Posted

Study publicly available on registry

March 1, 2021

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 30, 2021

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2021

Completed
Last Updated

March 1, 2021

Status Verified

February 1, 2021

Enrollment Period

3 months

First QC Date

February 6, 2021

Last Update Submit

February 24, 2021

Conditions

Keywords

Neural tissue mechanosensitivityDepressed Scapular AlignmentScapular upward rotation exercises

Outcome Measures

Primary Outcomes (1)

  • 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 Outcomes (1)

  • Pressure pain threshold

    All measurements were taken pre and post the treatment period (6 weeks).

Study Arms (1)

one group

EXPERIMENTAL

The treatment program consisted of upward rotation exercises for 3 sessions/week, for 6 weeks.

Other: Upward rotation exercise

Interventions

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

one group

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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).
  • The clavicle appeared to be horizontal or the acromioclavicular joint was lower than the sternoclavicular joint by visual appraisal.
  • The vertebral borders of the scapula was less than 3 inches from the spine by tape measure.

You may not qualify if:

  • Subject who has any of the following criteria was excluded from the study:
  • Subjects with cervical spinal fractures.
  • Neck-rotation ROM of \<20º.
  • Radiating pain to an upper extremity.
  • Scoliosis.
  • Leg length discrepancy.
  • A history of unresolved cancer.
  • Diabetes Miletus.
  • Polyneuropathy.
  • Myofascial Pain Syndrome.
  • Fibromyalgia.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Ragiaa Kamel

    Basic Science Department, Faculty of Physical Therapy, Cairo University

    STUDY CHAIR
  • Amr Shalaby

    Basic Science Department, Faculty of Physical Therapy, Cairo University

    STUDY DIRECTOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

February 6, 2021

First Posted

March 1, 2021

Study Start

February 28, 2021

Primary Completion

May 30, 2021

Study Completion

August 1, 2021

Last Updated

March 1, 2021

Record last verified: 2021-02

Data Sharing

IPD Sharing
Will share

I commit to share the results of this study within 3-6 months of publicatin.

Time Frame
I commit to share the results of this study within 3-6 months of publication.