Kinesiophobia in Chronic Neck Pain

Active, not recruiting

• Conditions: Neck Pain; Kinesiophobia

• Registration Number: NCT06849999
• Lead Sponsor: Fatih Sultan Mehmet Training and Research Hospital

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.

Detailed Description

Not available

Study Timeline

• Status Verified: 2025-02
• Study Start: 2025-02-15
• Study First Submitted: 2025-02-24
• Study First Submitted QC: 2025-02-24
• Last Update Submitted: 2025-02-24
• Study First Posted: 2025-02-27
• Last Update Posted: 2025-02-27
• Primary Completion: 2025-05-15
• Study Completion: 2025-05-15

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 57

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
tampa kinesiophobia scale	1 day
sf 36	1 day	Quality of Life

Trial Locations

Locations (1)

Liv hospital Vadistanbul; 🇹🇷 Istanbul, Turkey