Effects of Rigid Taping in Acromioclavicular Joint Degeneration
ACJTaping
The Effect of Rigid Taping on Pain and Function in Individuals With Acromioclavicular Joint
1 other identifier
interventional
28
1 country
1
Brief Summary
This study will examine whether rigid taping applied to the acromioclavicular (AC) joint can reduce shoulder pain and improve shoulder function in people with AC joint degeneration. Participants with shoulder pain and a confirmed diagnosis of AC joint degeneration will be randomly assigned to one of two groups: (1) rigid taping plus a standardized exercise program or (2) the same exercise program without taping. The program will last 4 weeks, with weekly supervised visits. Pain, shoulder motion, and shoulder function will be assessed at baseline, after the first session (acute effect), at the end of treatment (Week 4), and at a 3-month follow-up.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jan 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 30, 2025
CompletedStudy Start
First participant enrolled
January 1, 2026
CompletedFirst Posted
Study publicly available on registry
January 12, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 25, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2026
CompletedJanuary 12, 2026
December 1, 2025
3 months
December 30, 2025
December 30, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Pain Intensity
Pain intensity will be assessed at rest and during activity using the Visual Analog Scale (VAS).
Baseline (Week 0), immediately after the first session (acute effect), Week 4 (end of intervention), and Month 3 follow-up
Shoulder Range of Motion
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.
Baseline (Week 0), immediately after the first session (acute effect), Week 2, Week 4 (end of intervention), and Month 3 follow-up
Secondary Outcomes (1)
Shoulder Function
Baseline (Week 0), Week 4 (end of intervention), and Month 3 follow-up
Study Arms (2)
Rigid Taping + Exercise
ACTIVE COMPARATORParticipants will receive rigid acromioclavicular joint taping once weekly for 4 weeks in addition to a standardized shoulder exercise program supervised by a physiotherapist.
Exercise Only
ACTIVE COMPARATORParticipants will receive a standardized shoulder exercise program supervised by a physiotherapist without any taping application.
Interventions
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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hacettepe University, Faculty of Physical Therapy and Rehabilitation, Sports Physiotherapy and Rehabilitation Department
Ankara, Ankara, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor, PhD
Study Record Dates
First Submitted
December 30, 2025
First Posted
January 12, 2026
Study Start
January 1, 2026
Primary Completion
March 25, 2026
Study Completion
April 30, 2026
Last Updated
January 12, 2026
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared because specific data-sharing agreements and governance procedures have not been established.