The Relationship of Cervical Sagittal Parameters With Pain and Disability in Cervical Myofascial Pain Syndrome

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

133 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-09-01

Study Completion Date

2022-10-10

Brief Summary

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Participants between the ages of 18-64 who were diagnosed with cervical myofascial pain syndrome will be included in the study. cervical sagittal parameters, numerical pain rating scale, Bournemouth neck questionnaire and cervical range of motion will be measured and evaluated.

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Detailed Description

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It is an observational, cross-sectional study. Participants between the ages of 18-64 who were diagnosed with cervical myofascial pain syndrome, who applied to the Physical Medicine and Rehabilitation Clinic of Kanuni Sultan Süleyman Training and Research Hospital with neck pain for more than 3 months will be included. The pain level of the participants will be evaluated with the numerical pain rating scale, the cervical range of motion and the disability level with the Bournemouth neck questionnaire. C0-2 cervical lordosis angle, C2-C7 cervical lordosis angle, cervical sagittal vertical axis (cSVA), T1 slop, T1 slop - cervical lordosis angle (TS-CL), cervical tilt, thoracic inlet angle (TIA) and Cranial tilt measurement will be performed by using Surgimap software program. The relationship between the level of pain and disability, and cervical sagittal parameters will be evaluated.

Conditions

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Myofascial Pain Syndrome Neck Pain Neck Disorder

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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cervical myofascial pain syndrome

The participants who diagnosed as cervical myofascial pain syndrome aged 18-64 years. The pain must last at least 3 months.

no intervention

Intervention Type OTHER

there is no any intervention in this study. it is an observational and cross-sectional study.

Interventions

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no intervention

there is no any intervention in this study. it is an observational and cross-sectional study.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age at 18-64 years
* Neck pain due to myofascial pain syndrome for more than 3 months
* Presence of lateral cervical radiograph taken in neutral position in the last 3 months
* Visible lower border of T1 vertebra on lateral radiographs
* Absence of other spinal pathologies such as underlying scoliosis, cervical disc herniation, spondylolysis, spondylolisthesis

Exclusion Criteria

* Presence of an organic pathology that will cause neck pain
* Inability to see the lower border of the T1 vertebra on lateral cervical radiographs and the radiographs not taken in neutral position

Minimum Eligible Age

18 Years

Maximum Eligible Age

64 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No