Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
ID06674668

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

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Being between 18 and 65 years of age
  • Patients diagnosed with lateral epicondylitis
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

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)

Follow-up

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

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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

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