Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07333417

Effects of Rigid Taping in Acromioclavicular Joint Degeneration

Led by Hacettepe University · Updated on 2026-01-12

28

Participants Needed

1

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Effects of Rigid Taping in Acromioclavicular Joint Degeneration

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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 and to provide written informed consent
Not Eligible

You will not qualify if you...

  • Current or previous diagnosis or 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

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Hacettepe University, Faculty of Physical Therapy and Rehabilitation, Sports Physiotherapy and Rehabilitation Department

Ankara, Ankara, Turkey (Türkiye)

Actively Recruiting

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Research Team

I

Irem Duzgun, PhD, Prof

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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