Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07302282

The Effectiveness of Pain Neuroscience Education for Patients With Carpal Tunnel Syndrome

Led by Karamanoğlu Mehmetbey University · Updated on 2026-01-06

48

Participants Needed

1

Research Sites

33 weeks

Total Duration

On this page

Sponsors

K

Karamanoğlu Mehmetbey University

Lead Sponsor

K

Karaman Training and Research Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to investigate the effects of Pain Neuroscience Education applied in the treatment of mild and moderate carpal tunnel syndrome (CTS). The main question it aims to answer is: Does PNE have a therapeutic effect on carpal tunnel syndrome in clinical and ultrasonographic terms? Researchers will compare whether PNE creates a synergistic effect alongside home based exercise programs and splint application in mild to moderate CTS, and will objectively demonstrate potential benefits such as relief from pain and numbness.

CONDITIONS

Official Title

The Effectiveness of Pain Neuroscience Education for Patients With Carpal Tunnel Syndrome

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Being 18 years of age or older
  • Having a diagnosis of mild or moderate carpal tunnel syndrome confirmed by electrophysiological examination
  • Experiencing pain and numbness in the first three fingers of the hand for at least 3 months
Not Eligible

You will not qualify if you...

  • Presence of severe carpal tunnel syndrome on electrophysiological examination
  • Having uncontrolled diabetes or hypothyroidism
  • Having inflammatory rheumatic diseases such as rheumatoid arthritis
  • Having other neuromuscular diseases affecting the hand or wrist (e.g., polyneuropathy, cervical radiculopathy, brachial plexus damage)
  • History of trauma to the hand or wrist
  • History of neck or wrist surgery
  • Receiving steroid injection in the carpal tunnel within the last 3 months
  • Undergoing physical therapy on the wrist within the last 3 months
  • Wrist deformity preventing splint use
  • Previous participation in psychological management programs for chronic pain
  • Cognitive dysfunction interfering with cooperation in tests

AI-Screening

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Trial Site Locations

Total: 1 location

1

Karaman Training and Research Hospital

Karaman, Karaman, Turkey (Türkiye), 70200

Actively Recruiting

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Research Team

M

Mahmut Talha Susam, MD.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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