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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07025668
Enrollment
36
Registered
2025-06-17
Start date
2025-05-09
Completion date
2025-11-30
Last updated
2025-06-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sports Physical Therapy, Tendinopathy

Keywords

biceps brachii, tendinopathy, tendon cross-sectional area, shoulder pain

Brief 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.

Detailed description

There are different conservative treatment options for biceps brachii long head tendinopathy. However, the exercise approaches that can be applied for biceps brachii tendinopathy are not clear in the literature. This study aims to investigate the effectiveness of exercises that include 12 weeks of eccentric training or combined exercise approaches.

Interventions

OTHEREccentric 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.

OTHERCombined 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.

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.

Sponsors

Hacettepe University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Participants in all three groups performed the given exercises without knowing which group they were included in. Outcome assessments will be performed by an investigator who was blinded to group allocation.

Intervention model description

three groups with a conventional therapy control group

Eligibility

Sex/Gender
ALL
Age
18 Years to 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.

Design outcomes

Primary

MeasureTime frameDescription
Tendon Cross-Sectional AreaBaseline and 12 weeksUltrasound will be used to measure tendon cross-sectional area.

Secondary

MeasureTime frameDescription
Visual Analog Scale (VAS)Baseline and 12 weeksThe patient will be asked to mark the severity of his/her pain at rest, at night, and during general activity on a 10 cm line without numbers, and the point they mark will be measured in millimeters with a ruler. The left end of the line indicates no pain, corresponding to 0 cm, while the pain level increases towards the right end of the line, which is marked at 10 cm.

Countries

Turkey (Türkiye)

Contacts

Primary ContactEbru G SEZİK, Msc
ebrugulozdemiir@gmail.com05532025875

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026