Actively Recruiting
Radial Shock Waves Versus Focal Shock Waves in the Treatment of Lateral Epicondylalgia
Led by University of Alcala · Updated on 2026-06-02
50
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Lateral epicondylalgia (LET), a condition marked by elbow pain, reduced wrist extensor muscle strength, and disability, is the focus of this study. Researchers aim to compare the safety and effectiveness of two types of shockwave therapies—radial shockwave therapy and focal shockwave therapy—in managing the symptoms of LET. The study will measure changes in elbow pain, grip strength, and disability over a six-month period. Participants will be randomly assigned to one of three groups: one receiving radial shock waves, another receiving focal shock waves, and a control group receiving a placebo treatment with very low energy settings. Each participant will undergo three treatment sessions, with one session per week. The radial shock wave group will receive 2000 pulses at 2.5 bars pressure and 8 Hz frequency, while the focal shock wave group will receive 2000 pulses at 0.2 mJ/mm² energy flux density and 4 Hz frequency. The placebo group will receive 20 pulses per session at 0.08 mJ/mm² energy flux density. Throughout the study, researchers will assess participants' elbow pain using a Visual Analog Scale (VAS), grip strength with a handheld dynamometer, and disability through the Patient-Rated Tennis Elbow Evaluation Questionnaire (PRTEE). Additionally, the Global Rating of Change (GROC) will be measured. Follow-up assessments will be conducted for six months to monitor changes from baseline. The study is randomized and triple-blinded to ensure objective evaluation of the treatments.
CONDITIONS
Brief Title
Treatment of Lateral Epicondylalgia With Shock Waves
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pain in the lateral epicondyle lasting more than 3 months
- Pain when performing resisted grip
- Positive Cozen test
- Positive Maudsley test
- Age between 18 and 70 years
You will not qualify if you...
- Pregnancy
- Systemic diseases such as fibromyalgia, diabetes, or arthritis
- Local infection or cancer
- Recent treatments like physiotherapy or corticosteroids
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Three sessions over a few weeks
Participants receive one of three interventions involving shock wave therapy, consisting of three treatment sessions with either radial shock waves, focal shock waves, or a placebo treatment.
3 treatment visits
Duration - 6 months
Participants are monitored to assess pain, grip strength, and functional improvement up to 6 months after treatment.
Periodic visits during 6 months
Trial Site Locations
Total: 1 location
1
Centro Investigación Fisioterapia y Dolor
Alcalá de Henares, Madrid, Spain, 28806
Actively Recruiting
Research Team
Y
Yanira Rodriguez-García, Master
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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