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

Sponsor
Kanuni Sultan Suleyman Training and Research Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05225571
Collaborator
(none)
200
1
12.3
16.3

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: no intervention

Detailed Description

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.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
200 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
The Relationship of Cervical Sagittal Parameters With Pain and Disability in Cervical Myofascial Pain Syndrome
Actual Study Start Date :
Sep 1, 2021
Anticipated Primary Completion Date :
Jul 10, 2022
Anticipated Study Completion Date :
Sep 10, 2022

Arms and Interventions

Arm Intervention/Treatment
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.

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

Outcome Measures

Primary Outcome Measures

  1. NRS (Numerical rating scale) [1 day]

    The Numeric Rating Scale (NRS) is the simplest and most commonly used numeric scale in which the child rates the pain from 0 (no pain) to 10 (worst pain)

  2. cervical range of motion (degree) [1 day]

    cervical flexion, extension, lateral flexion and rotation angles are actively evaluated.

  3. Bournemouth Neck Questionnaire [1 day]

    Adapted from the Bournemouth Low Back Pain questionnaire developed by Bolton and Humphreys in 2002. The Bournemouth Neck Pain Questionnaire consists of 7 questions in total. Each question scores between 0 and 10. Although the highest score is 70, a high score indicates a high level of disability.

  4. cervical sagittal parameters [1 day]

    Parameters to be checked in cervical lateral radiograph; C0-2 and C2-7 lordosis, T1 slope, c2-7 sagittal vertical axis, TS-CL, servical tilt and cranial tilt.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 64 Years
Sexes Eligible for Study:
All
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kanuni Sultan Suleyman TRH Istanbul Kucukcekmece Turkey 34303

Sponsors and Collaborators

  • Kanuni Sultan Suleyman Training and Research Hospital

Investigators

  • Principal Investigator: Merve Damla Korkmaz, Kanuni Sultan Suleyman Training and Research Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Merve Damla Korkmaz, Principal investigator, Kanuni Sultan Suleyman Training and Research Hospital
ClinicalTrials.gov Identifier:
NCT05225571
Other Study ID Numbers:
  • KAEK/2021.05.146
First Posted:
Feb 4, 2022
Last Update Posted:
Jun 3, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Merve Damla Korkmaz, Principal investigator, Kanuni Sultan Suleyman Training and Research Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 3, 2022