Kinesiophobia in Chronic Neck Pain

NCT ID: NCT06849999

Last Updated: 2025-02-27

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Total Enrollment: 57 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2025-02-15
• Study Completion Date: 2025-05-15

Brief Summary

In this study, the effect of kinesiophobia on pain, disability, and quality of life in individuals with chronic neck pain will be evaluated. Neck pain is a common musculoskeletal disorder that can become chronic in some individuals. Kinesiophobia may lead to a reduction in physical activity due to fear of movement and re-injury, thereby increasing pain and disability. In this cross-sectional study, 57 participants will be assessed using the Visual Analog Scale (VAS), Tampa Scale for Kinesiophobia (TSK), Neck Disability Index (NDI), and the SF-36 Quality of Life Scale. Participants will be selected from individuals aged 18-59 who have experienced neck pain for at least 3 months, and those with a history of neurological disorders, spinal surgery, or pain treatment in the last 3 months will be excluded. This research aims to determine the effects of kinesiophobia on chronic neck pain, thereby contributing to the development of more effective treatment strategies. Written informed consent will be obtained from all participants.

Conditions

Neck Pain; Kinesiophobia

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: CROSS_SECTIONAL

Eligibility Criteria

Inclusion Criteria

• Adults aged 18 to 59
• Patients of both genders experiencing neck pain for at least 3 months

Exclusion Criteria

• Patients with neurological deficits
• Patients with any neurological disorder
• Patients with a history of spinal fractures, spinal tumors, or spinal infections
• Patients with a history of spinal surgery
• Patients with any congenital spinal anomaly
• Patients with vestibular disorders
• Patients taking antidepressant and antihypertensive medications
• Patients unwilling to participate in the study
• Patients who have received any pain treatment in the last 3 months
• Patients who have engaged in any strenuous physical activity within the 24 hours prior to the assessment

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 59 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Fatih Sultan Mehmet Training and Research Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

pmr specialist

Role: PRINCIPAL_INVESTIGATOR

Liv hospital vadistanbul

Locations

Liv hospital Vadistanbul

Istanbul, Istanbul, Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

FSM PRH boyun

Identifier Type: -

Identifier Source: org_study_id