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Status unknownNCT04775251Updated Mar 1, 2021

Scapular Upward Rotation Exercises for Subjects With Deperessed Scapular Alignment

An interventional study of Upward rotation exercise in Scapular Dyskinesis, sponsored by Cairo University. Status unknown. Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-03-01.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Feb 2021), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Not applicable
Ages
18 Years to 30 Years
Sex
All
01

Study 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.

Read the detailed 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.

02

Conditions studied

  • Scapular Dyskinesis

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Keywords

  • Neural tissue mechanosensitivity
  • Depressed Scapular Alignment
  • Scapular upward rotation exercises
03

In context

Dyskinesias

270 studies on the registry are indexed under Dyskinesias; 41 are open to participants now.

This study's planned enrollment of 30 is below the median of 44 across 192 interventional studies indexed under Dyskinesias.

Browse Dyskinesias studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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 \<20º.
    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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    one group

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

    Other: Upward rotation exercise

Interventions

  • OtherUpward rotation exercise

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

06

What researchers measure

Primary outcomes

  1. Neural excitability

    Neural excitability measured by Strenght-duration cruve.

    Time frame: 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

    Pressure pain threshold was measured using pressure algometer.

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

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

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

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 1, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04775251
Lead sponsor
Cairo University
Responsible party
Doha Hamed Moustafa Al-Afifi (Principal investigator, Cairo University) — Principal investigator
First posted
Mar 1, 2021
Start date
Feb 28, 2021 (estimated)
Primary completion
May 30, 2021 (estimated)
Completion
Aug 2021 (estimated)
Last update
Mar 1, 2021

Study contacts

Doha Al-Afifi
Contact
doha.h.afifi@gmail.com
01003169353
Ragiaa Kamel
study chair · Basic Science Department, Faculty of Physical Therapy, Cairo University
Amr Shalaby
study director · Basic Science Department, Faculty of Physical Therapy, Cairo University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Feb 2021. You cannot join it, but the record below documents what was studied.

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