Actively Recruiting

Phase Not Applicable
Age: 20Years - 65Years
All Genders
NCT07432425

Effects of Different Exercise Protocols on Physical and Cognitive Changes in People With Chronic Neck Pain

Led by Hacettepe University · Updated on 2026-02-25

21

Participants Needed

1

Research Sites

47 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to investigate the effects of different exercise approaches on physical status, cognitive functions, brain structures, and blood biomarkers in individuals with chronic neck pain.

CONDITIONS

Official Title

Effects of Different Exercise Protocols on Physical and Cognitive Changes in People With Chronic Neck Pain

Who Can Participate

Age: 20Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants aged 20 to 65 years
  • Having neck pain for at least 3 months with a pain score of 3 or more on the Numeric Rating Scale
  • Scoring 10 or higher on the Neck Disability Index
  • Scoring 24 or above on the Mini Mental State Examination
  • Being right-handed according to the Edinburgh Handedness Inventory
  • Having completed at least primary school education
Not Eligible

You will not qualify if you...

  • Having neuropsychiatric, neurologic, metabolic, cardiovascular, or inflammatory diseases
  • Participated in a rehabilitation program for neck pain within the last 6 months
  • Having an exercise or sports history of 6 months or more
  • Having brain lesions visible on MRI
  • Having non-removable metal objects or devices incompatible with MRI
  • History of neck or shoulder surgery
  • Being pregnant or having given birth within the last year

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hacettepe University Faculty of Physical Therapy and Rehabilitation

Ankara, Altindag, Turkey (Türkiye)

Actively Recruiting

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Research Team

Z

Zeynep Güven, MsC

CONTACT

S

Songul Atasavun-Uysal, Professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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