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Comparative Effects of Shockwave Therapy and Eccentric Exercises in Patients With Lateral

The goal of this randomized controlled trial is to compare the effects of shockwave therapy and eccentric exercises on pain, functional ability, quality of life, grip strength and range of motion in patients with lateral epicondylitis. Participants will be randomly assigned to either Group A (Shockwave therapy) or Grou

Condition(s)Tennis Elbow
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryThe goal of this randomized controlled trial is to compare the effects of shockwave therapy and eccentric exercises on pain, functional ability, quality of life, grip strength and range of motion in patients with lateral epicondylitis. Participants will be randomly assigned to either Group A (Shockwave therapy) or Group B (Eccentric Exercises) using a computer-generated random number tables method. The intervention will be provided over five weeks, with three sessions per week (total of 15 sessions): Group A (Shockwave therapy): Participants will receive shockwave therapy, for 5 min with energy level 7.0 m J and frequency 6 Hz. Group B (Eccentric Exercises): Participants will receive eccentric exercises, repeating each 10 repetitions 3 sets per session with a 1 min rest between each of the
Who can participateInclusion Criteria: * Patients diagnosed with Lateral epicondylitis * Patients with 20-50 years * Both males and females * Willing to participate and provide informed consent Exclusion Criteria: * Patients with recent trauma (fractures, injury etc.) * Patients with blood clotting disorder (including thrombosis), oral anti-coagulants, and pacemaker, tumors at site of treatment, infected area or skin rupture or abrasion at the site of treatment, pregnancy. * Cervical Radiculopathy or any diseases that mimic or refer pain to elbow. * Patients who received steroid injection within 6 weeks.
Ages20 Years to 50 Years
SexAll
Lead sponsorIbadat International University, Islamabad
LocationsIslamabad, Pakistan
Start date2026-02-02
NCT IDNCT07523893
Official listinghttps://clinicaltrials.gov/study/NCT07523893

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