The Effect of Biomechanical Scapular Mobilization With Movement and Motor Learning
BSMWM
1 other identifier
interventional
38
1 country
1
Brief Summary
the study about new mobilization technique used in shoulder impingement syndrome patient to increase the range of motion of elevation, decrease the pain, and increasing the function level, this technique is based on normal mechanics that occur inside the joint during certain movement.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2021
Shorter than P25 for not_applicable
1 active site
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
January 5, 2021
CompletedFirst Posted
Study publicly available on registry
January 8, 2021
CompletedResults Posted
Study results publicly available
April 14, 2021
CompletedStudy Start
First participant enrolled
May 5, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 22, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
November 14, 2021
CompletedMay 18, 2022
April 1, 2022
6 months
January 5, 2021
January 8, 2021
April 29, 2022
Conditions
Outcome Measures
Primary Outcomes (2)
Visual Analogue Scale
1\. Visual Analogue Scale: was used to evaluate the intensity of pain, which The pain VAS is a continuous scale comprised of a horizontal (HVAS) or vertical (VVAS) line, usually, 10 centimetres in length, anchored by 2 verbal descriptors, one for each symptom extreme. For pain intensity, the scale is most commonly anchored by "no pain" (score of 0) and "pain as bad as it could be" or "worst imaginable pain" (score of 10 centimetres).
3 weeks
Universal Goniometer
Universal goniometer: was used to measure the available range of motion at a joint. where used to measure an available range of motion of abduction and flexion of the shoulder joint.
3 weeks
Study Arms (2)
group A (controlled group)
ACTIVE COMPARATORreceived passive range of motion (PROM)/ active assisted range of motion (AAROM)/ active range of motion (AROM) exercises, strengthen of rotator cuff, biceps, shoulder and scapular muscles, ultrasound (5 min. - 1.5 W/c.m2 - 1 MHZ), electrical stimulation ( interferential bipolar technique for 20 min. on shoulder joint). This treatment was repeated three times per weeks with 24 hours rest for 3 weeks.
group B(Study group)
ACTIVE COMPARATORAll patients in group B received biomechanical scapular mobilization with movement and motor learning and traditional methods.
Interventions
the therapist applied posterior tilt and exteral rotation with upward rotation mobilization to scapula and therapist also warp bilt around GH joint to applied inferior and posterior glid then ask patient to elevate his arm. then we applied motor learning approach by asking patient to elevate his arm with maintaining of external rotation with posterior glid of scapula.
Eligibility Criteria
You may qualify if:
- clinical diagnosis: shoulder impingement syndrome.
- History of shoulder pain when they elevated their arm.
- Limited range of motion due to the pain.
- Pain localized at the painful point at proximal anterolateral shoulder region or medical diagnosis of shoulder impingement syndrome with at least 2 positive impingement tests including Neer, Hawkins, or Jobe test.
You may not qualify if:
- Fibromyalgia.
- Fracture, dislocation, or subluxation of the shoulder.
- history of trauma.
- shoulder surgery.
- numbness or tingling in the upper limb.
- Corticosteroids injection within 1 year.
- systemic illness.
- ligamentous laxity
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Pharos university in Alexandria
Alexandria, Egypt
Related Publications (1)
Surenkok O, Aytar A, Baltaci G. Acute effects of scapular mobilization in shoulder dysfunction: a double-blind randomized placebo-controlled trial. J Sport Rehabil. 2009 Nov;18(4):493-501. doi: 10.1123/jsr.18.4.493.
PMID: 20108851RESULT
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Results Point of Contact
- Title
- P.T Moataz Abdelaal
- Organization
- Pharos university in Alexandria
Study Officials
- STUDY CHAIR
Moataz A. Mohamed, (B.Sc.P.T.)
Pharos University in Alexandria
Publication Agreements
- PI is Sponsor Employee
- Yes
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Demonstrator in Faculty of Physical Therapy, Pharos University, Alexandria, Egypt.
Study Record Dates
First Submitted
January 5, 2021
First Posted
January 8, 2021
Study Start
May 5, 2021
Primary Completion
October 22, 2021
Study Completion
November 14, 2021
Last Updated
May 18, 2022
Results First Posted
April 14, 2021
Record last verified: 2022-04