Evaluating the effect of Tecar therapy in patients with shoulder impingement syndrome

Not Applicable

Recruiting

• Conditions: Impingement syndrome of shoulder.; Impingement syndrome of shoulder; M75.4

• Registration Number: IRCT20190618043931N4
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 January 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Diagnosis of shoulder impingement syndrome by physical medicine and rehabilitation specialist with physical examination
Age 20-70 years
Duration of pain more than one month
Visual analog scale more than 3

Exclusion Criteria

Patients who have a history of shoulder surgery.
Patients who have undergone rehabilitation treatments in the last 3 months due to shoulder pain.
Existence of neurological disease, infectious disease, cognitive disorder, malignancy
Low patient compliance
The presence of a pacemaker
Existence of heart and kidney disease

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: before treatment, immediately after last session, 3 months after treatment. Method of measurement: Visual Analogue Scale questionnaire.;Shoulder joint abduction range of motion. Timepoint: before treatment, immediately after last session, 3 months after treatment. Method of measurement: Goniometer.;The degree of shoulder disability. Timepoint: before treatment, immediately after last session, 3 months after treatment. Method of measurement: The Disabilities of the Arm, Shoulder and Hand Score questionnaire.