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Chronic Non-Specific Neck Pain and Quality of Life

Investigation of Factors Affecting Quality of Life in Chronic Non-Specific Neck Pain

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06777862
Enrollment
70
Registered
2025-01-16
Start date
2024-12-20
Completion date
2025-07-13
Last updated
2025-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain, Quality of Life

Keywords

chronic neck pain, quality of life, depression, proprioception, muscle strength

Brief summary

The factors affecting the quality of life in individuals with chronic non-specific neck pain are not fully known in the studies conducted to date. The aim of this study was to examine the factors affecting the quality of life of individuals with chronic non-specific neck pain.

Interventions

None listed

Sponsors

Kirsehir Ahi Evran Universitesi
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

No history of radicular pain, trauma or surgery in the cervical region, * Between the ages of 18-65, * Having neck pain for at least 6 months, * Not having received any treatment for neck pain in the last year * Volunteers with chronic non-specific neck pain

Exclusion criteria

* Those with any systemic disease * Those with cervical pathology * Previous surgery in the neck region * Those with neuromuscular disease * Those with rheumatology disease * Infection

Design outcomes

Primary

MeasureTime frameDescription
Pain Level6 weeksVisual Analog Scale (VAS) will be used to assess the severity of the patient's neck pain. The participant is asked to mark the severity of the pain on a 10-centimeter line (0=no pain, 10=very much pain)

Secondary

MeasureTime frameDescription
MUSCLE STRENGTH6 weeksIn order to obtain objective data, maximal isometric muscle strength of the cervical region muscles will be measured with a Lafayette brand portable dynamometer. During the measurements, participants are asked to generate maximum force against the portable dynamometer device throughout the test (3-5 seconds).
Cervical Region Proprioception Sense6 weeksJoint position sense will be evaluated in four directions: left rotation, right rotation, extension and flexion with the Cervical Joint Position Sense Test. A total of ten measurements will be made, the first four for trial purposes. The average of the last six measurements will be taken for each direction.
Depression symptoms6 weeksBeck Depression Inventory (BDI) will be used to assess depression symptoms. The scale consists of 21 items, each of which is scored from 0 to 3. Higher scores indicate the severity of depression (1-10 points = normal, 11-16 points = moderate mood disturbance, 17-20 points = clinical depression, 21-30 points = moderate depression, 31-40 points = severe depression, 41-63 points = severe depression).
RANGE OF MOTION6 weeksClinical goniometer will be used to measure the flexion, extension, lateral flexion and rotation range of motion of the cervical spine.
Sleep Quality6 weeksThe participants' sleep quality will be assessed with the Pittsburgh Sleep Quality Index (PSQI). The scale consists of seven components (subjective sleep quality, time it takes to fall asleep, sleep duration, sleep disorders, use of medication for sleep, habitual efficiency of sleep and daily life dysfunction). Each component is valued between 0-5 points. The total score is 0-21 points (\<5 points = good sleep quality, \>5 points disturbed sleep quality).
Neck Disability Level6 weeksNeck Disability Questionnaire will be used to evaluate disability due to neck pain. The questionnaire consists of 10 questions. The questionnaire evaluates the intensity of pain in the neck region, difficulty in personal care and work, headache, pain level while reading, lifting performance, driving, difficulty level in sleeping and leisure activities. Each question is evaluated with 0-5 points and increasing score is associated with increasing disability. A high total score indicates that the individual's neck disability rate increases. (0-20 points = minimal disability, 21-40 points = moderate disability, 41-60 points = severe disability, 61-80 points = disability, 81-100 points = bedridden
Quality of Life Level6 weeksThe participants' quality of life will be assessed with the Short Form Health Survey -36 Quality of Life Scale. The scale consists of 36 statements and has 8 subheadings (physical function, pain, mental status, physical role limitation, emotional role limitation, vitality, social function and general perception of health). As the total score increases, the quality of life also increases. Scores for these scales are standardized into values ranging from 0 to 100 with 50 representing average health.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026