RecruitingNot ApplicableNCT06735092

Exercise Therapy and Orthoses in Lateral Elbow Tendinopathy: Comparative Effects

Investigation of the Effects of Different Types of Orthoses Used in Addition to Exercise Therapy in Lateral Elbow Tendinopathy


Sponsor

Istanbul University - Cerrahpasa

Enrollment

45 participants

Start Date

Dec 2, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Inclusion Criteria5

  • Being between the ages of 18 and 65,
  • Having a diagnosis of unilateral lateral elbow tendinopathy,
  • Having at least two of the Thomsen, Maudley's, Mill's, or Cozen's tests positive during clinical examination,
  • Experiencing symptoms for at least 3 months,
  • Not having a systemic or chronic illness that would prevent participation in the treatment program.

Exclusion Criteria5

  • A history of trauma or surgery in the relevant elbow and/or wrist,
  • The presence of orthopedic and/or neurological problems in the cervical spine, shoulder joint, or wrist,
  • Participation in a physiotherapy and rehabilitation program for lateral elbow tendinopathy within the last 6 months,
  • Receiving any injections within the last 6 months,
  • Systemic inflammation.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERExercise-Only Group (Control Group)

Participants in this group will only undergo a standardized exercise protocol. The exercises will be part of a program lasting 6 weeks, conducted 2 days per week. A combined evidence-based exercise program consisting of wrist isometric, concentric, and eccentric exercises will be applied to the individuals in the group. For free-weight exercises, participants will start with weights of 0.5-1 kg, tailored to the individual. Progression will be achieved with 0.5-1 kg increments. For exercises using resistance bands, the increase in resistance will be provided by selecting the next level band color. Participants will be assessed before treatment, at the end of the 6th week, and at the end of the 12th week.

OTHERExercise + Forearm Counterforce Brace Group

Participants in this group will undergo a standardized exercise protocol and will be provided with a counterforce forearm brace in addition to exercise therapy. The exercises will be part of a program lasting 6 weeks, conducted 2 days per week. A combined evidence-based exercise program consisting of wrist isometric, concentric, and eccentric exercises will be applied to the individuals in the group. For free-weight exercises, participants will start with weights of 0.5-1 kg, tailored to the individual. Progression will be achieved with 0.5-1 kg increments. For exercises using resistance bands, the increase in resistance will be provided by selecting the next level band color. Participants will be assessed before treatment, at the end of the 6th week, and at the end of the 12th week.

OTHERExercise + Wrist Brace Group

Participants in this group will undergo a standardized exercise protocol and will be provided with a wrist brace in addition to exercise therapy. The exercises will be part of a program lasting 6 weeks, conducted 2 days per week. A combined evidence-based exercise program consisting of wrist isometric, concentric, and eccentric exercises will be applied to the individuals in the group. For free-weight exercises, participants will start with weights of 0.5-1 kg, tailored to the individual. Progression will be achieved with 0.5-1 kg increments. For exercises using resistance bands, the increase in resistance will be provided by selecting the next level band color. Participants will be assessed before treatment, at the end of the 6th week, and at the end of the 12th week.


Locations(1)

Faculty of Health Sciences, Istanbul University - Cerrahpasa

Istanbul, Buyukcekmece, Turkey (Türkiye)

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06735092


Related Trials