Actively Recruiting
Immediate Effect of Wearable Vibrotactile Stimulation on Pain and Sense in Patients with Lateral Epicondylitis
Led by Medipol University · Updated on 2024-11-05
33
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
Sponsors
M
Medipol University
Lead Sponsor
T
The Scientific and Technological Research Council of Turkey
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to study the immediate effects of vibrotactile stimulation on pain, sensation, and function in people with lateral epicondylitis, a chronic condition affecting the tendons around the elbow. The condition, often called tennis elbow, results in pain and reduced grip strength due to sensory changes rather than tendon damage. The study focuses on comparing wearable vibration technology combined with traditional physiotherapy against physiotherapy alone to understand their impacts on symptoms and upper limb function. Participants will be randomly assigned to one of two groups. Both groups will receive one session of traditional physiotherapy, including wrist stretching exercises, radial head mobilization, and deep friction massage on the affected arm. The intervention group will also wear a vibrotactile device on the affected area for 20 minutes while resting comfortably. Immediate effects will be measured before and after the treatment session. During the study, participants will undergo assessments of pain severity, pressure pain threshold, and joint position sense before and about one hour after treatment. Secondary measures include hand grip sensitivity, grip strength, and a functional assessment after two weeks. The study is double-blinded and randomized, ensuring unbiased evaluation. Participation lasts for the treatment session and includes follow-up assessments to evaluate short-term functional improvements.
CONDITIONS
Brief Title
Effect of Vibrotactile Stimulation in Lateral Epicondylitis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Being between 18 and 65 years of age
- Patients diagnosed with lateral epicondylitis
You will not qualify if you...
- Having had elbow surgery
- Having a history of congenital or acquired orthopedic, neurological, or rheumatological conditions affecting the upper limb
- Having received any conservative treatment for the diagnosis of lateral epicondylitis
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.
Duration - Single session
Participants receive traditional physiotherapy involving passive stretching exercises, radial head mobilization, and deep friction massage on the affected extremity. Those in the intervention group also use a wearable vibrotactile device during the session.
1 visit (in-person)
Duration - 2 weeks
Participants are assessed for functional outcomes approximately 2 weeks after treatment.
1 follow-up visit
Trial Site Locations
Total: 1 location
1
Istanbul Kultur University
Istanbul, Turkey (Türkiye)
Actively Recruiting
Research Team
I
Imge NAS
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here