Effect of TECAR (Transfer of Energy Capacitive and Resistive) Therapy on Chronic Supraspinatus Tendinitis
NCT ID: NCT07316712
Last Updated: 2026-01-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
46 participants
INTERVENTIONAL
2025-12-30
2026-02-28
Brief Summary
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Detailed Description
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The supraspinatus tendon, part of the rotator cuff of the shoulder joint, is particularly affected. Aging is also a common factor leading to supraspinatus tendon injuries. The primary function of the supraspinatus muscle is shoulder abduction, particularly during movements that elevate the arm overhead. During these motions, the supraspinatus tendon repeatedly passes beneath the acromion process of the scapula, which can result in impingement and subsequent inflammation. An unexpected force or trauma may cause a partial or complete tendon rupture if this condition progresses.
Transfer of Energy Capacitive and Resistive (TECAR) offers a unique variety of treatments for chronic and acute pathologies, with contraindications such as pregnancy, pacemakers, and sensitivity to high temperatures. It should be noted that this new technology is a valuable tool in treating various pathologies, particularly when compared with other therapies in terms of the presence and/or absence of specific positive effects. TECAR also has distinct characteristics that are effective even when other treatments fail. This therapy balances the therapist's manual skills and the specialized energy that this technology offers, resulting in increasingly satisfactory outcomes for therapists and patients.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Conventional treatment + TECAR therapy
The experimental group will receive conventional physiotherapy sessions as the active comparator group, in addition to TECAR therapy at the end of each session. Sessions will be received for three weeks (nine sessions, three times per week).
Conventional treatment
All patients in both groups will receive conventional treatment, 3 sessions per week for 3 weeks. The conventional methods for treating supraspinatus tendinitis include shoulder swings, painless range of motion (ROM) exercises, shoulder joint active-assisted exercises, resistance exercises to improve muscle strength, and pain-reducing physiotherapy modalities like ultrasound.
TECAR (Transfer of Energy Capacitive and Resistive) Therapy
Patients in the experimental group only will receive TECAR therapy, 3 sessions per week for 3 weeks. The treatment will start with an automatic capacitive energy transfer for 10 minutes. Next, the capacitive plaque will be replaced by the resistive electrode, and the neutral electrode will be fixed
Conventional treatment
The active comparator group will receive conventional physiotherapy sessions for three weeks (nine sessions, three times per week).
Conventional treatment
All patients in both groups will receive conventional treatment, 3 sessions per week for 3 weeks. The conventional methods for treating supraspinatus tendinitis include shoulder swings, painless range of motion (ROM) exercises, shoulder joint active-assisted exercises, resistance exercises to improve muscle strength, and pain-reducing physiotherapy modalities like ultrasound.
Interventions
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Conventional treatment
All patients in both groups will receive conventional treatment, 3 sessions per week for 3 weeks. The conventional methods for treating supraspinatus tendinitis include shoulder swings, painless range of motion (ROM) exercises, shoulder joint active-assisted exercises, resistance exercises to improve muscle strength, and pain-reducing physiotherapy modalities like ultrasound.
TECAR (Transfer of Energy Capacitive and Resistive) Therapy
Patients in the experimental group only will receive TECAR therapy, 3 sessions per week for 3 weeks. The treatment will start with an automatic capacitive energy transfer for 10 minutes. Next, the capacitive plaque will be replaced by the resistive electrode, and the neutral electrode will be fixed
Eligibility Criteria
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Inclusion Criteria
* All patients will have a body mass index between 18.5 and 29.9 kg/m².
Exclusion Criteria
* Any past shoulder surgical interventions.
* Instability of the shoulder joint due to other reasons, Acromioclavicular Joint Arthritis.
* Non-cooperative subjects.
* Diabetes
* Pregnant or lactating women.
* Serious neuromuscular or cardiovascular diseases.
* Systemic illness and severe COVID-19 cases will be excluded from this study.
* Pacemakers
* Heat Sensitivity
* Metal Implants
30 Years
55 Years
ALL
No
Sponsors
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Cairo University
OTHER
Responsible Party
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Mohamed Gamal Ibrahem Alghamry
Principal Investigator
Principal Investigators
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Hanaa Kenawy Atta, PhD
Role: STUDY_CHAIR
Assistant Professor, Cairo University
Hend Hamdy Mohamed Ahmed, PhD
Role: STUDY_DIRECTOR
Lecturer, Cairo university
Locations
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CAN Center outpatient clinic
Cairo, , Egypt
Countries
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Central Contacts
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Hend Hamdy Mohamed Ahmed, PhD
Role: CONTACT
Facility Contacts
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Other Identifiers
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P.T.REC/012/005900
Identifier Type: -
Identifier Source: org_study_id
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