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Clinical Trials in Turkey / NCT07025668
Recruiting Not applicable

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

NCT07025668 · tracked via the Priya Life Science Turkey tracker
Sponsor
Hacettepe University
Phase
Not applicable
Started
2025-05-09
Last updated
2025-06-17

Condition(s) studied

Sports Physical TherapyTendinopathy

Investigational drug(s) / intervention(s)

Eccentric ExerciseCombined ExerciseControl Group Exercise

Eccentric Exercise: In the eccentric exercise group, in addition to strengthening exercises for the periscapular muscles and stretching exercises for the biceps brachii muscle, eccentric strengthening exercises for the biceps brachii muscle will be given. Participants will do the exercises in the groups they were randomized to every day for 12 weeks. They will be called to the clinic once a week for exercise checks.

Combined Exercise: In the combined exercise group, in addition to strengthening exercises for the periscapular muscles and stretching exercises for the biceps brachii muscle, progressive isometric, isotonic and plyometric strengthening training will be given to the biceps brachii muscle. Participants will do the exercises in the groups they were randomized to every day for 12 weeks. They will be called to the clinic once a week for exercise checks.

Control Group Exercise: In the control group, strengthening exercises for the periscapular muscles and stretching exercises for the biceps brachii muscle will be given. Strengthening exercises for the biceps brachii muscle will not be given in this group. Participants will do the exercises in the groups they were randomized to every day for 12 weeks. They will be called to the clinic once a week for exercise checks.

Study summary

This study was planned to analyze the changes in tendon cross-sectional area and shoulder pain with different exercise approaches applied in biceps brachii long head tendinopathy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
50 Years
Healthy volunteers
No
Inclusion Criteria: * Having shoulder pain lasting 3 months or more * Without a history of surgery, having a diagnosis of shoulder rotator cuff tendinopathy, rotator cuff stage 1-2 tear or subacromial impingement, and having been diagnosed with secondary biceps long head tendinopathy by a physician * Pain level during activity \> 3 according to the visual analog scale * Patients who have been informed about the study and have given written consent to participate in the study will be included in the study. Exclusion Criteria: * Acute shoulder injury * History of shoulder and cervical surgery * Limitation of passive range of motion * History of local corticosteroid injection within the last 12 months * Patients who cannot comply with the exercise program will be excluded from the study.

Primary outcome measure(s)

  • Tendon Cross-Sectional Area — Baseline and 12 weeks
    Ultrasound will be used to measure tendon cross-sectional area.

Trial sites (1)

FacilityCityRegionStatus
Hacettepe University Faculty of Physical Therapy and Rehabilitation Ankara Turkey (Türkiye) Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07025668 on ClinicalTrials.gov ↗ ← All trials in Turkey