- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07333417
Effects of Rigid Taping in Acromioclavicular Joint Degeneration (ACJTaping)
The Effect of Rigid Taping on Pain and Function in Individuals With Acromioclavicular Joint
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Shoulder pain is one of the most common musculoskeletal complaints and can affect daily activities, work, and sports participation. Among the potential sources of shoulder pain, the acromioclavicular (AC) joint is a distinct pain generator that can often be identified through a targeted clinical examination. Diagnosis is typically based on a detailed history combined with physical tests designed to provoke AC joint symptoms, such as scarf maneuvers and localized palpation.
The AC joint is a synovial articulation between the distal clavicle and the acromion of the scapula. Although its motion is relatively limited, it plays an important role in load transfer across the shoulder girdle, particularly during arm elevation and overhead activities. AC joint symptoms may arise through different mechanisms, including degenerative changes over time, traumatic events, or inflammatory processes. Degenerative AC joint disease may coexist with other shoulder conditions, and structural changes around the joint can contribute to pain by increasing mechanical stress and altering the subacromial environment. As a result, individuals may experience pain with overhead movements, cross-body motions, lifting, pushing, or during sport-specific tasks.
Management of AC joint degeneration typically begins with conservative care. Common non-surgical strategies include physiotherapy, activity modification, temporary unloading or immobilization when needed, and symptom-directed medical management. Rehabilitation approaches generally focus on optimizing posture, improving scapular control, enhancing periscapular strength and endurance, restoring flexibility of the posterior shoulder structures, and progressively reintroducing functional loading while minimizing symptom provocation.
Taping techniques are frequently used in shoulder rehabilitation as an adjunct to exercise-based care. In clinical practice, rigid and elastic taping methods are applied with the intention of modifying joint alignment and mechanical loading, limiting painful movement patterns, and supporting more efficient scapulothoracic and glenohumeral mechanics during activity. Rigid taping, in particular, is often considered when a more structured mechanical effect is desired. While taping has been investigated in various shoulder pain presentations, existing evidence has largely focused on subacromial pain conditions and scapular kinematics rather than AC joint degeneration specifically. Consequently, there remains uncertainty about whether rigid taping provides additional clinical benefit for individuals whose primary pain source is degenerative change at the AC joint.
Therefore, the purpose of this study is to evaluate the effects of rigid AC joint taping on shoulder pain, pain-free shoulder range of motion, and shoulder function in individuals with shoulder pain associated with AC joint degeneration.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Irem Duzgun, PhD, Prof
- Phone Number: +90 (312) 305 15 74
- Email: iremduzgun@hacettepe.edu.tr
Study Locations
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Ankara
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Ankara, Ankara, Turkey (Türkiye)
- Recruiting
- Hacettepe University, Faculty of Physical Therapy and Rehabilitation, Sports Physiotherapy and Rehabilitation Department
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- A clinical diagnosis of acromioclavicular (AC) joint degeneration confirmed by clinical examination and imaging (X-ray, ultrasound, or MRI).
- Shoulder pain duration of at least 4 weeks.
- Age between 18 and 65 years
- Willingness to refrain from any additional treatments outside the study protocol during the study period (e.g., medication changes, injections, or physiotherapy elsewhere) and to provide written informed consent
Exclusion Criteria:
- Current or previous diagnosis/history of acromioclavicular (AC) joint separation.
- Diagnosis of frozen shoulder (adhesive capsulitis).
- History of acute trauma or fracture involving the shoulder girdle (e.g., clavicle fracture, shoulder dislocation).
- History of shoulder surgery.
- Systemic inflammatory joint disease (e.g., rheumatoid arthritis) or other systemic arthropathies.
- Skin conditions preventing taping (e.g., rash, open wound, or known tape allergy).
- Neuromuscular disease or neurological disorders affecting shoulder function
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Rigid Taping + Exercise
Participants will receive rigid acromioclavicular joint taping once weekly for 4 weeks in addition to a standardized shoulder exercise program supervised by a physiotherapist.
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Rigid taping will be applied to the acromioclavicular joint using a standardized technique aiming to posteriorize the acromion and inferiorize the clavicle.
Taping will be performed once weekly for 4
A standardized shoulder exercise program focusing on soft tissue flexibility, scapular stabilization, and rotator cuff activation will be applied once weekly for 4 weeks.
|
|
Active Comparator: Exercise Only
Participants will receive a standardized shoulder exercise program supervised by a physiotherapist without any taping application.
|
A standardized shoulder exercise program focusing on soft tissue flexibility, scapular stabilization, and rotator cuff activation will be applied once weekly for 4 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Intensity
Time Frame: Baseline (Week 0), immediately after the first session (acute effect), Week 4 (end of intervention), and Month 3 follow-up
|
Pain intensity will be assessed at rest and during activity using the Visual Analog Scale (VAS).
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Baseline (Week 0), immediately after the first session (acute effect), Week 4 (end of intervention), and Month 3 follow-up
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Shoulder Range of Motion
Time Frame: Baseline (Week 0), immediately after the first session (acute effect), Week 2, Week 4 (end of intervention), and Month 3 follow-up
|
Shoulder range of motion (flexion, abduction, internal rotation, and external rotation) will be assessed using a goniometer by recording active range of motion until pain onset, active range of motion despite pain, and passive end-range of motion.
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Baseline (Week 0), immediately after the first session (acute effect), Week 2, Week 4 (end of intervention), and Month 3 follow-up
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Shoulder Function
Time Frame: Baseline (Week 0), Week 4 (end of intervention), and Month 3 follow-up
|
Shoulder function will be evaluated using the American Shoulder and Elbow Surgeons Shoulder Score (ASES), which assesses pain and functional activities of daily living.
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Baseline (Week 0), Week 4 (end of intervention), and Month 3 follow-up
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pain
- Neurologic Manifestations
- Musculoskeletal Diseases
- Joint Diseases
- Arthralgia
- Pathological Conditions, Signs and Symptoms
- Signs and Symptoms
- Shoulder Pain
- Motor Activity
- Movement
- Musculoskeletal Physiological Phenomena
- Musculoskeletal and Neural Physiological Phenomena
- Therapeutics
- Physical Therapy Modalities
- Patient Care
- Exercise Therapy
- Rehabilitation
- Aftercare
- Continuity of Patient Care
- Physical Conditioning, Human
- Exercise
- Resistance Training
Other Study ID Numbers
- ACJTaping
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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