NCT07333417

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

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
28

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 30, 2025

Completed
2 days until next milestone

Study Start

First participant enrolled

January 1, 2026

Completed
11 days until next milestone

First Posted

Study publicly available on registry

January 12, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 25, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2026

Completed
Last Updated

January 12, 2026

Status Verified

December 1, 2025

Enrollment Period

3 months

First QC Date

December 30, 2025

Last Update Submit

December 30, 2025

Conditions

Keywords

Shoulder painAcromioclavicular joint degenerationRigid taping

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 COMPARATOR

Participants will receive rigid acromioclavicular joint taping once weekly for 4 weeks in addition to a standardized shoulder exercise program supervised by a physiotherapist.

Other: Rigid TapingOther: Exercise Program

Exercise Only

ACTIVE COMPARATOR

Participants will receive a standardized shoulder exercise program supervised by a physiotherapist without any taping application.

Other: Exercise Program

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

Rigid Taping + Exercise

A standardized shoulder exercise program focusing on soft tissue flexibility, scapular stabilization, and rotator cuff activation will be applied once weekly for 4 weeks.

Exercise OnlyRigid Taping + Exercise

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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)

RECRUITING

MeSH Terms

Conditions

Shoulder Pain

Interventions

Resistance Training

Condition Hierarchy (Ancestors)

ArthralgiaJoint DiseasesMusculoskeletal DiseasesPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Exercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy ModalitiesPhysical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Outcome assessments are planned to be conducted by an assessor blinded to group allocation whenever possible.
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.

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