NCT04701814

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

87
On Track

Trial Health Score

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

Enrollment
38

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started May 2021

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 5, 2021

Completed
3 days until next milestone

First Posted

Study publicly available on registry

January 8, 2021

Completed
3 months until next milestone

Results Posted

Study results publicly available

April 14, 2021

Completed
21 days until next milestone

Study Start

First participant enrolled

May 5, 2021

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 22, 2021

Completed
23 days until next milestone

Study Completion

Last participant's last visit for all outcomes

November 14, 2021

Completed
Last Updated

May 18, 2022

Status Verified

April 1, 2022

Enrollment Period

6 months

First QC Date

January 5, 2021

Results QC Date

January 8, 2021

Last Update Submit

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 COMPARATOR

received 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.

Other: biomechanical scapular mobilization with movement and motor learning

group B(Study group)

ACTIVE COMPARATOR

All patients in group B received biomechanical scapular mobilization with movement and motor learning and traditional methods.

Other: biomechanical scapular mobilization with movement and motor learning

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.

group A (controlled group)group B(Study group)

Eligibility Criteria

Age25 Years - 50 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Location

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.

MeSH Terms

Conditions

Shoulder Impingement Syndrome

Interventions

Movement

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal DiseasesShoulder InjuriesWounds and Injuries

Intervention Hierarchy (Ancestors)

Physiological PhenomenaMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Results Point of Contact

Title
P.T Moataz Abdelaal
Organization
Pharos university in Alexandria

Study Officials

  • Moataz A. Mohamed, (B.Sc.P.T.)

    Pharos University in Alexandria

    STUDY CHAIR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Patients were divided randomly in two equal groups (A and B): Group A (controlled group): They were received traditional physical therapy program including: passive range of motion (PROM)/ active assisted range of motion (AAROM)/ active range of motion (AROM), 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). Group B (study group): they have received the same physical therapy program as in group A, in addition to Biomechanical scapular mobilization with movement and motor learning.
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

Locations