Comparative Effects of Shockwave Therapy and Eccentric Exercises in Patients With Lateral Epicondylitis
1 other identifier
interventional
50
1 country
1
Brief Summary
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 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 them. Outcomes will be assessed at baseline, week 0 and week 5 to evaluate which exercise program is more effective in reducing symptoms and improving functional outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 2, 2026
CompletedFirst Submitted
Initial submission to the registry
April 5, 2026
CompletedFirst Posted
Study publicly available on registry
April 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 16, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 30, 2026
April 13, 2026
April 1, 2026
4 months
April 5, 2026
April 5, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
Pain Intensity
Pain intensity will be measured by Visual Analogue Scale
Assessment will be done at baseline and on Week 5
Functional Ability
Functional ability will be measured by Patient-Related Tennis Elbow Evaluation
Assessment will be done at baseline and on Week 5
Quality of Life of Patients
Quality of Life will be measured by SF-36 short form
Assessment will be done at baseline and on Week 5
Grip Strength
Grip Strength will be measured by Dynamometer
Assessment will be done at baseline and on Week 5
Range of Motion
Range of Motion will be measured by Goniometer.
Assessment will be done at baseline and on Week 5
Study Arms (2)
Shock Wave Therapy
EXPERIMENTALParticipants will receive shockwave therapy, for 5 min with energy level 7.0 m J and frequency 6 Hz.
Eccentric exercises
EXPERIMENTALParticipants will receive eccentric exercises, repeating each exercise 10 repetitions 3 sets per session with a 1 min rest between each of them
Interventions
Participants will receive shockwave therapy, for 5 min with energy level 7.0 m J and frequency 6 Hz.
Participants will receive eccentric exercises, repeating each 10 repetitions 3 sets per session with a 1 min rest between each of them
Eligibility Criteria
You may qualify if:
- Patients diagnosed with Lateral epicondylitis
- Patients with 20-50 years
- Both males and females
- Willing to participate and provide informed consent
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of Allied Health & Biological Sciences
Islamabad, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Muhammad Nazim Farooq, PhD-PT
Ibadat International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Masking Details
- Participants will be informed that both interventions are effective physiotherapy treatments for lateral epicondylitis but will not be told which group they belonged to. The outcome assessor will remain blinded to group allocation throughout data collection at baseline and week 5. To maintain blinding, participants will be instructed not to disclose their exercise details during assessment, and all data will be recorded using coded identifiers (Group A or B).
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 5, 2026
First Posted
April 13, 2026
Study Start
February 2, 2026
Primary Completion (Estimated)
June 16, 2026
Study Completion (Estimated)
June 30, 2026
Last Updated
April 13, 2026
Record last verified: 2026-04