Status:

COMPLETED

Influence of Radial Extracorpeal Shock Wave in Hemiplegic Shoulder Patients

Lead Sponsor:

Delta University for Science and Technology

Conditions:

Hemiplegia

Spastic

Eligibility:

All Genders

30-60 years

Phase:

NA

Brief Summary

The purposes of this study are to examine sonographic structural changes pre and post the radial extracorporeal shock wave intervention in hemiplegic shoulder pain, and to assess the relationships bet...

Detailed Description

Painful shoulder is a common complication following hemiplegic stroke. This pain may interfere with functional improvement, the patient's quality of life, and it may impede the process of rehabilitati...

Eligibility Criteria

Inclusion

  • 1\. Patient's age ranges from 40 to 60 years. 2. Spasticity of upper limb ranges from mild to moderate (grade 1+: 2) according to modified aschworth scale (MAS).
  • 3\. Patients with sufficient cognitive abilities that enables them to understand and follow instructions (Mini-Mental Scale \>24).
  • 4\. Patient who understand the study process and signed the informed consent form.
  • 5\. Patient with stroke more than 3 months ago. 8. Patient with shoulder pain and limited range of motion (ROM) or loss of motion in the proximal arm on the hemiplegic side.

Exclusion

  • The following patients will be excluded from the study:
  • Patients who cannot express their own pain intensity.
  • Patients with a history of trauma or surgery to the shoulder on the affected side.
  • Patients with history of oral NSAIDs 3 days before this study or take warfarin medication with an international normalized ratio above 4.0.
  • Patients with a history of shoulder pain before the stroke.
  • 6\. Patients who have received a previous shoulder intra-articular injection or other interventions on the affected shoulder within one month before rESWT.
  • 7\. Patients with cardiac pacemaker. 8. Patients who have osteoporosis. 9. Patients with psychological problems.

Key Trial Info

Start Date :

June 1 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 1 2021

Estimated Enrollment :

30 Patients enrolled

Trial Details

Trial ID

NCT04859673

Start Date

June 1 2021

End Date

September 1 2021

Last Update

February 16 2023

Active Locations (1)

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Cairo university

Cairo, Egypt