Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06735092

Exercise Therapy and Orthoses in Lateral Elbow Tendinopathy: Comparative Effects

Led by Istanbul University - Cerrahpasa · Updated on 2024-12-16

45

Participants Needed

1

Research Sites

45 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study is to address the inconsistencies in the literature by investigating the effects of a forearm counterforce brace and a wrist splint, used in addition to exercise therapy, on pain, functionality, and grip strength in individuals diagnosed with lateral elbow tendinopathy, compared to those receiving exercise therapy alone.The findings aim to provide valuable insights into clinical practice by highlighting the roles of both orthosis use and exercise in the treatment of lateral elbow tendinopathy.

CONDITIONS

Official Title

Exercise Therapy and Orthoses in Lateral Elbow Tendinopathy: Comparative Effects

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Be between 18 and 65 years old
  • Have a diagnosis of unilateral lateral elbow tendinopathy
  • Have at least two positive tests among Thomsen, Maudley's, Mill's, or Cozen's during clinical exam
  • Have symptoms lasting at least 3 months
  • Not have any systemic or chronic illness that would prevent participation in the treatment program
Not Eligible

You will not qualify if you...

  • History of trauma or surgery in the affected elbow and/or wrist
  • Have orthopedic or neurological problems in the cervical spine, shoulder joint, or wrist
  • Participated in physiotherapy or rehabilitation for lateral elbow tendinopathy within the last 6 months
  • Received any injections in the affected area within the last 6 months
  • Have systemic inflammation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Faculty of Health Sciences, Istanbul University - Cerrahpasa

Istanbul, Buyukcekmece, Turkey (Türkiye), 34500

Actively Recruiting

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Research Team

B

Büşra Kültür, MSc (c)

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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