Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
ID07025668

Effects of Different Exercise Approaches on Tendon Cross-sectional Area and Pain in Biceps Brachii Long Head Tendinopathy

Led by Hacettepe University · Updated on 2025-06-17

36

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate different exercise approaches for biceps brachii long head tendinopathy, a condition causing shoulder pain. The study focuses on how these exercises affect tendon size and pain levels. It compares the effects of eccentric training versus combined exercise methods over a 12-week period to find the best approach for managing this tendinopathy. Participants are randomly assigned to one of three groups. One group performs eccentric strengthening exercises for the biceps brachii along with periscapular muscle strengthening and stretching. Another group receives combined progressive isometric, isotonic, and plyometric strengthening exercises in addition to the same baseline exercises. The control group performs only periscapular strengthening and biceps brachii stretching without specific biceps strengthening. All exercises are done daily for 12 weeks, with weekly clinic visits for exercise monitoring. During the study, researchers measure the tendon cross-sectional area and shoulder pain using a visual analog scale at the start and after 12 weeks. Participants will be evaluated weekly to ensure adherence and proper exercise performance. The study's total duration includes the 12-week exercise period, with assessments focused on tendon changes and pain improvement to understand the impact of each exercise approach.

CONDITIONS

Brief Title

The Effectiveness of Different Exercise Approaches in Biceps Brachii Long Head Tendinopathy

Who Can Participate

Age: 18Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Having shoulder pain lasting 3 months or more
  • Diagnosed by a physician with secondary biceps long head tendinopathy along with shoulder rotator cuff tendinopathy, rotator cuff stage 1-2 tear, or subacromial impingement
  • Pain level during activity greater than 3 on the visual analog scale
  • Provided written consent after being informed about the study
Not Eligible

You will not qualify if you...

  • Acute shoulder injury
  • History of shoulder or cervical surgery
  • Limitation of passive range of motion
  • Local corticosteroid injection within the last 12 months
  • Inability to comply with the exercise program

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 12 weeks

Participants perform daily exercises according to their assigned group: eccentric exercises, combined isometric/isotonic/plyometric exercises, or periscapular strengthening and biceps stretching only. They attend weekly clinic visits for exercise checks.

Weekly visits for exercise checks

Trial Site Locations

Total: 1 location

1

Hacettepe University Faculty of Physical Therapy and Rehabilitation

Ankara, Turkey (Türkiye)

Actively Recruiting

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Research Team

E

Ebru G SEZİK, Msc

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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