Actively Recruiting

Phase Not Applicable
Age: 20Years - 65Years
All Genders
ID07432425

Effects of Different Exercise Protocols on Physical Status, Cognitive Functions, Brain Structure, and Blood Biomarkers in People With Chronic Neck Pain

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

21

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to explore how different types of exercises affect physical health, cognitive functions, brain structure, and blood markers in adults with chronic neck pain. Chronic neck pain often comes with physical and cognitive challenges, but the exact brain and biochemical reasons are not fully understood. The study focuses on improving these issues by using exercise programs known to support both physical and cognitive well-being. Participants will be randomly assigned to one of three groups: aerobic exercise, strengthening exercise, or posture and stretching exercises as a control. Each group will complete 36 individual exercise sessions over 12 weeks, exercising three times per week. Aerobic training involves cycling at varying intensities and durations, while strengthening exercises include specific neck and upper body resistance training. The control group will perform posture and stretching exercises. During the study, participants will undergo detailed assessments before and after the exercise program, including tests of attention, memory, language, and executive function, as well as brain imaging to observe structural and blood flow changes. Physical evaluations will measure pain levels, neck disability, muscle strength, function, and sleep quality. Blood samples will be collected to analyze various biochemical markers. Muscle strength and functional capacity will also be checked at week six to adjust exercise intensity. Pain intensity will be tracked at baseline, week six, and week twelve, with all data helping researchers understand how different exercises impact people with chronic neck pain.

CONDITIONS

Brief 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
  • Neck pain lasting at least 3 months with a pain score of 3 or more on the Numeric Rating Scale
  • Neck Disability Index score of 10 or higher
  • Mini Mental State Examination score of 24 or above
  • Right-handed according to Edinburgh Handedness Inventory
  • At least primary school education completed
Not Eligible

You will not qualify if you...

  • Presence of neuropsychiatric, neurologic, metabolic, cardiovascular, or inflammatory diseases
  • Participation in a rehabilitation program for neck pain during the past 6 months
  • Exercise or sports activity history of 6 months or more
  • Brain parenchymal lesion detected on MRI
  • Presence of non-removable materials like metal, pacemaker, or hearing aid unsuitable for MRI
  • History of neck or shoulder surgery
  • Pregnancy 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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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 12 weeks

Participants receive one of three exercise programs: aerobic exercise, strengthening exercise, or posture and stretching exercise as a control. Exercise sessions occur 3 days a week for 12 weeks, totaling 36 individual sessions.

3 sessions per week for 12 weeks

Follow-up

Duration - Assessment at 6th week within treatment period

Participants have assessments of muscle strength and functional capacities at the end of the 6th week to monitor progress during the exercise program.

1 mid-exercise assessment visit

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

S

Songul Atasavun-Uysal, Professor

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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