NCT06789991

Brief Summary

this study aims to assess the gluteus maximus muscle electromyographic activity and the latissimus dorsi muscle electromyographic activity in patients with shoulder impingement syndrome , to improve the assessment procedure and the rehabilitation program for treating patients with shoulder impingement syndrome more effectively. .

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Study Start

First participant enrolled

January 1, 2025

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

January 16, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

January 23, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2025

Completed
Last Updated

January 23, 2025

Status Verified

January 1, 2025

Enrollment Period

3 months

First QC Date

January 16, 2025

Last Update Submit

January 22, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • • electromyographic activity of posterior oblique sling muscles (gluteus maximus and latissimus dorsi)

    EMG has been widely used for many decades, its use is proven and widely accepted by clinicians and the scientific community and it is considered the gold standard method for the measurement of muscle activity.

    through study completion, an average of 4 months

Secondary Outcomes (3)

  • shoulder active range of motion

    through study completion, an average of 4 months

  • shoulder function and disability level

    through study completion, an average of 4 months

  • shoulder pain

    through study completion, an average of 4 months

Study Arms (2)

Group A (control group)

controls

Device: electromyography

Group B (experimental group)

cases

Device: electromyography

Interventions

electromyographic activity of posterior oblique sling muscles will be measured

Group A (control group)Group B (experimental group)

Eligibility Criteria

Age25 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

All patients will be referred by an orthopedic surgeon who will diagnose SIS based on clinical and radiological examination.

You may qualify if:

  • Both male and female patients with shoulder impingement syndrome.
  • patients complain from unilateral shoulder pain with chronic conditions of SIS ≥ 3 months.
  • Patient age from 25 to 40 years.
  • Patients with Positive impingement tests.
  • Patients with painful arc of movement (60°- 120°)

You may not qualify if:

  • Patients with Numbness or tingling of upper extremity.
  • Patients with Shoulder fracture or previous shoulder surgery, and Acromioclavicular or shoulder dislocation.
  • Patients with Any traumatic injury to the lower limb in the previous 6 months.
  • Any spine surgery within the last 2 years.
  • Patients with history of lower back pain in past 12 months .
  • Patients with history of lower extremity dysfunctions in the past 12 months .
  • Participants who had taken any drugs (e.g. statins and spasmed), which have effects on the skeletal muscles.
  • Open wounds, rashes, psoriasis, skin irritations, or skin conditions of any kind in the region of electrode placement
  • Participants with a Body Mass Index (BMI) ≥ 30

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cairo University

Cairo, Giza Governorate, 12613, Egypt

Location

MeSH Terms

Conditions

Shoulder Impingement Syndrome

Interventions

Electromyography

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal DiseasesShoulder InjuriesWounds and Injuries

Intervention Hierarchy (Ancestors)

ElectrodiagnosisDiagnostic Techniques and ProceduresDiagnosisMyography

Study Officials

  • Soheir S Rizk, PhD

    Cairo University

    STUDY CHAIR
  • Aya A Khalil, PhD

    Cairo University

    STUDY DIRECTOR

Central Study Contacts

nada M emara, BSc

CONTACT

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principle investigator

Study Record Dates

First Submitted

January 16, 2025

First Posted

January 23, 2025

Study Start

January 1, 2025

Primary Completion

April 1, 2025

Study Completion

April 1, 2025

Last Updated

January 23, 2025

Record last verified: 2025-01

Data Sharing

IPD Sharing
Will not share

Locations