Ireland
--:--IST
Recruiting Not applicable

TECAR With Chronic Shoulder Impingement Syndrome

NCT07919249 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-11-04
Last updated
2026-11-09

Condition(s) studied

Shoulder Impingement Syndrome

Investigational drug(s) / intervention(s)

TECAR therapyPassive TECAR therapyconventional exerciseConventional exercise:

TECAR therapy: TECAR therapy: Received for 8 sessions during the intervention period. Each session consisted of 20 minutes: 10 minutes in capacitive mode at 100 W, followed by 10 minutes in resistive mode at 200 W. The device was operated at a pulsed frequency,

Passive TECAR therapy: sham treatment by TECAR device for 20 min without producing any waves.

conventional exercise: The program included three stretching exercises to address soft tissue restriction. It specifically targeted the upper trapezius, pectoralis minor, and posterior shoulder capsule. Each stretch was held for 30 seconds and repeated three times, with 30 seconds between repetitions Following the stretching exercises, participants completed a progressive strengthening program targeting the rotator cuff muscles and scapular stabilization. Participants performed strengthening exercises using color-coded elastic resistance bands, with 3 sets of 10 repetitions and 1 minute of rest between sets. Rotator cuff strengthening consisted of shoulder flexion, Abduction, External rotation, and Internal Rotation exercises. Scapular stabilization exercises included serratus anterior, middle trapezius, and lower trapezius muscle strengthening)

Conventional exercise:: The program included three stretching exercises to address soft tissue restriction. It specifically targeted the upper trapezius, pectoralis minor, and posterior shoulder capsule. Each stretch was held for 30 seconds and repeated three times, with 30 seconds between repetitions Following the stretching exercises, participants completed a progressive strengthening program targeting the rotator cuff muscles and scapular stabilization. Participants performed strengthening exercises using color-coded elastic resistance bands, with 3 sets of 10 repetitions and 1 minute of rest between sets. Rotator cuff strengthening consisted of shoulder flexion, Abduction, External rotation, and Internal Rotation exercises. Scapular stabilization exercises included serratus anterior, middle trapezius, and lower trapezius muscle strengthening)

Study summary

The study aimed to investigate the adjunctive effects of TECAR therapy in combination with conventional exercises compared with placebo TECAR combined with the same exercise program on pain intensity, shoulder function, range of motion, and muscle strength in individuals with subacromial syndrome.

Eligibility

Sex
ALL
Min age
30 Years
Max age
55 Years
Healthy volunteers
No
Inclusion Criteria: * Referred by an orthopedic physician with a clinical diagnosis (confirmed by imaging examination-magnetic resonance imaging or ultrasound) of Tendinopathy of any muscle of the Rotator cuff and pain in the shoulders for at least 3 months * Participants ranged in age from 30 to 55 years old * Numerical pain rating scale (NPRS)≥4: * Four of the following should be present in the included patients: Neer impingement test, Hawkins' test, Pain was replicated in the supraspinatus empty-can test, a painful arc of movement from 70° to 120°, and pain at the greater tuberosity of the humerus * BMI range 18.5- 29. 9 Kg/m². Exclusion Criteria: * Patients who have a full-thickness rotator cuff tear. * History of shoulder or rotator cuff surgery or fracture, glenohumeral joint dislocation, rheumatoid arthritis (affected side). * Pharmacological medical treatment that may interfere with the measurements; history of corticosteroid injections in the last three months. * Patients who received rehabilitation therapy in the last 3 months. * Patients who have symptoms of numbness or tingling in the upper extremity. * A history of the following: onset of symptoms due to traumatic injury. * Patients who have cognitive or psychiatric disorders or pregnancy. * Patients who have a positive Drop arm sign. * Patients who have cervical radiculopathy.

Primary outcome measure(s)

  • Numerical pain Rating scale: — 6 weeks
    The NPRS was used to assess the patient's shoulder pain intensity. Patients rated their current pain level on an 11-point scale from 0 (no pain) to 10 (worst pain imaginable). Ask participants to mark the point on the pain intensity scale
  • Shoulder function using the Shoulder Pain and Disability Index Questionnaire (SPADI): — 6 weeks
    The SPADI test consists of 13 items divided into two domains: the pain domain (5 items) and the disability domain (8 items). Each item is assigned a value from 0 to 10 on the NRS; the score ranges from 0 (no difficulty) to 10 (unable to perform). All the responses' ratings will be added and divided by the number of questions in that subscale. The total SPADI score will be calculated as the average of the 2 subscales

Trial sites (1)

FacilityCityRegionStatus
outpatient orthopedic clinics of the Faculty of Physical Therapy, Cairo University. Cairo Egypt Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07919249 on ClinicalTrials.gov ↗ ← All trials in Egypt