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Effect of Transfer Energy Capacitive Resistive Therapy on Shoulder Pain and Function in Shoulder Impingement Syndrome

Effect of Transfer Energy Capacitive Resistive Therapy on Shoulder Pain and Function in Shoulder Impingement Syndrome

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06595641
Enrollment
30
Registered
2024-09-19
Start date
2024-10-01
Completion date
2025-03-01
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Impingement Syndrome, Shoulder

Keywords

Strengthening Exercises, Shoulder Impingement Syndrome, Transfer energy capacitive and resistive

Brief summary

This study investigates the efficacy of combining Transfer Energy Capacitive and Resistive (TECAR) therapy with standard strengthening exercises in treating Shoulder Impingement Syndrome (SIS). A double-blinded randomized controlled trial will compare outcomes between patients receiving only strengthening exercises and those receiving both TECAR therapy and exercises. Key outcomes include improvements in pain, muscle strength, joint position sense, and shoulder function. The study aims to determine if TECAR therapy enhances treatment benefits beyond those achieved with exercises alone.

Detailed description

Background: Shoulder Impingement Syndrome (SIS) is a prevalent musculoskeletal condition characterized by pain and functional impairment due to the compression of rotator cuff tendons beneath the coracoacromial arch. Despite the effectiveness of conservative treatments such as strengthening exercises, there is emerging interest in additional modalities, including Transfer Energy Capacitive and Resistive (TECAR) therapy. TECAR therapy utilizes high-frequency electromagnetic waves to provide deep thermal energy, potentially enhancing tissue repair and pain relief. Objective: This study aims to evaluate the effectiveness of combining TECAR therapy with a standard strengthening exercise regimen compared to strengthening exercises alone in patients with SIS. Methods: A double-blinded randomized controlled trial will be conducted with 30 participants diagnosed with Neer's Stage I SIS. Participants will be randomly assigned to either a control group receiving only strengthening exercises or an experimental group receiving both TECAR therapy and strengthening exercises. The study will assess pain, shoulder muscle strength, joint position sense, and shoulder function using a range of validated instruments including the Visual Analogue Scale (VAS), Hand-Held Dynamometer (HHD), Digital Inclinometer, and the Shoulder Pain and Disability Index (SPADI).

Interventions

DEVICETransfer Energy Capacitive Resistive Therapy

It's a physical treatment modality commonly used to treat musculoskeletal pain. It normally uses a longwave radiofrequency of \ 0.5 MHz. The system consists of a neutral plate and two different electrodes that can transfer energy in two modalities: capacitive and resistive

Each session includes five exercises, each performed for three sets of 10 repetitions: Shoulder Retraction - Strengthens muscles between shoulder blades. Shoulder Scaption - Improves stability and range of motion. Shoulder External Rotation from Side Lying - Targets rotator cuff muscles. Shoulder Protraction - Enhances shoulder blade function. Shoulder Extension - Strengthens posterior shoulder muscles

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

Double-blinded randomized controlled trial

Eligibility

Sex/Gender
ALL
Age
25 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Both gender age from 25-40 with a clinical diagnosis of Neer's stage II SIS and body mass index (18.5-29.9) * Shoulder pain for at least three months * Painful arc of movement during flexion or abduction * Positive Neer's or kennedy- hawkins test or empty can test * Pain on resisted external rotation, abduction

Exclusion criteria

* Symptoms of cervical radiculopathy. * Diagnosed inflammatory disorder. * Neurological disorder. * Widespread pain condition. * Evidence of complete rotator cuff tear (positive drop arm test). * Previous surgery to the affected shoulder. * Noncompliance patient. * Pacemaker.

Design outcomes

Primary

MeasureTime frameDescription
Visual Analog Scale3 weekswhich rates pain intensity from 0 (no pain) to 10 (worst possible pain)

Secondary

MeasureTime frameDescription
Manual Muscle Test System (MMT)3 weekswill be used to obtain normative strength values for both external and internal shoulder rotators .
Joint Position Sense of the Shoulder joint3 weeksAll participants will be submitted to the evaluation of the JPS at 30° and 120° of shoulder forward flexion, using a digital inclinometer
shoulder Function Using the Arabic SPADI Questionnaire3 weeksThe Arabic SPADI is recommended for the evaluation of Arabic-speaking patients with shoulder dysfunction . To answer the questions, patients will be asked to place a mark on a 10 cm visual analogue scale for each question. Verbal anchors for the pain dimension are 'no pain at all' and 'worst pain imaginable', and those for the functional activities are 'no difficulty' and 'so difficult, it required help'. The scores from both dimensions are averaged to derive a total score

Contacts

Primary ContactMostafa Mohamed Abdelkhalek, B.Sc
drmostafamohamedgalal@gmail.com929-435-8403
Backup Contactahmed mohamed khalil, PhD
ahmedazizkhalil90@gmail.com929-435-8403

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026