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Effectiveness of Radial Extracorporeal Shock Wave Therapy and Supervised Exercises in Lateral Epicondylitis

Comparison of the Effectiveness of Radial Extracorporeal Shock Wave Therapy and Supervised Exercises in the Treatment of Lateral Epicondylitis: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03834090
Enrollment
41
Registered
2019-02-07
Start date
2015-02-20
Completion date
2016-01-15
Last updated
2019-02-07

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

Conditions

Lateral Epicondylitis

Brief summary

No consensus has yet been built on the treatment of lateral epicondylitis (LE) due to the lack of evidence. Although conflicting results are present, radial extracorporeal shock wave therapy (rESWT) has increasingly been used in the treatment of tendinopathy

Detailed description

ESWT and exercise have beneficial effects on the management of tendinopathies owing to their various mechanisms that showed therapeutic efficacy. Owing to its positive outcomes, extracorporeal shock wave therapy (ESWT) has recently been used in the treatment of musculoskeletal system diseases such as plantar fasciitis, Achilles tendinopathy, calcific rotator cuff tendinopathies, and patellar tendinopathy

Interventions

DEVICErESWT

rESWT was administered once per week for 3 weeks using a ShockMaster 500 device with 1.8 bar pneumatic pressure, 10 Hz frequency, with 2000 pulses.

A program including post-isometric relaxation, and progressive resistance exercise (eccentric wrist extension) on the wrist extensors

Sponsors

Istanbul University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* The diagnosis of LE was made in the clinical examination, and the diagnosis was confirmed with the Southampton Diagnostic Criteria of the presence of epicondyle pain, and epicondyle pain and tenderness on resisted extension of the wrist. * Patients with symptoms lasting longer than 3 months * with average pain in the previous week detected as 3 or above on a 10-cm visual analogue scale (VAS) * who were aged over 18 years

Exclusion criteria

* pain in the proximal part of the affected extremity (e.g. shoulder pain, neck pain) * abnormal neurogenic symptoms (e.g. radicular pain, numbness) on the affected extremity * presence of posterior interosseous nerve entrapment * congenital or acquired upper extremity deformities that might affect grip strength * systemic musculoskeletal system or neurologic disorders * systemic rheumatologic disease or systemic infection * presence of malignancy, coagulation disorders, and anticoagulant use * inserted cardiac pacemaker * history of surgical treatment on the elbow of the affected extremity * pregnancy. * patients who were administered other treatments such as physical therapy or steroid injections in the last 3 months

Design outcomes

Primary

MeasureTime frameDescription
Change Patient-rated Tennis Elbow Evaluation scoreChange from Baseline at 1 month and 3 months after treatment.The Patient-rated Tennis Elbow Evaluation is a specific questionnaire designed for the evaluation of the disease-specific pain and function/disability in LE. The scores were calculated separately and as the total PRTEE score, where 0 represented the best score, and 100 represented the worst score. The PRTEE consists of a pain scale with 5 items questioning pain during rest and specific activities (0 represents 'no pain' and 10 represents 'the highest pain'), and a function/disability scale with 10 items evaluating difficulties experienced during specific and daily activities (0 represents 'no difficulty' and 10 represents 'the highest difficulty)

Secondary

MeasureTime frameDescription
Change Visual Analogue Scale scoreChange from Baseline at 1 month and 3 months after treatment.The self-evaluation of pain severity during rest and activity in the previous week was calculated using a 10-cm VAS scale
Change Roles and Maudsley ScoreChange from Baseline at 1 month and 3 months after treatment.The Roles and Maudsley score was used to evaluate pain and activity limitation as classified in four categories: 1 point = excellent, no pain, complete movement, and complete activity; 2 points = good, discomfort from time to time, complete movement, and complete activity; 3 points = fair, discomfort after long-duration activity; and 4 points = poor, pain that restricts activity.
Change Grip Strength scoreChange from Baseline at 1 month and 3 months after treatment.Grip strength of the affected upper extremity was calculated using a Hydraulic Hand Dynamometer

Outcome results

None listed

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