RecruitingNCT06413667

Assessment of the Alignment of the Atlas and Surrounding Tissues in Chronic Whiplash Associated Disorder


Sponsor

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Enrollment

90 participants

Start Date

Apr 8, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

Whiplash is an injury caused by the rapid forward and backward movement of the neck, leading to injuries in bones or soft tissues, along with various symptoms. Recent studies indicate that muscles affected by whiplash may show increased fat buildup and reduced muscle volume. However, these changes in muscle do not completely account for the pain and other symptoms reported. Besides soft tissues, whiplash can also injure bone structures, including the cervical spine. Until now, studies focused mainly on fractures of the cervical spine, often overlooking the position and alignment of the atlas and dens (C1 and C2). The aim of this study is to evaluate the position and alignment of the Atlas in chronic whiplash-associated disorder (grades 1 or 2) and compare it to patients with tension headache and healthy controls. Additionally, it will explore how these factors relate to pain intensity, neck movement limitations, daily activities, overall improvement, and quality of life.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Inclusion Criteria16

  • Control participants In order to be eligible to participate in this study, a participant must meet the following criteria:
  • Healthy individuals
  • Ability to follow test instructions
  • Aged between 18 - 75 years
  • Chronic Whiplash Associated Disorder
  • In order to be eligible to participate in this study, a participant must meet the following criteria:
  • Healthy individuals
  • Ability to follow test instructions
  • WAD 1 or 2 Diagnosis
  • Aged between 18 - 75 years
  • Tension headache
  • In order to be eligible to participate in this study, a participant must meet the following criteria:
  • Healthy individuals
  • Ability to follow test instructions
  • Diagnosis Tension headache
  • Aged between 18 -75 years

Exclusion Criteria5

  • Inability to provide informed consent
  • Have a history of claustrophobia
  • Patient/ participant is not eligible to follow instructions
  • Contra-indication for MRI (e.g., pacemaker, claustrophobia)
  • Being under investigation for non-diagnosed disease at the time of investigation

Interested in this trial?

Get notified about updates and connect with the research team.


Locations(1)

Amsterdam UMC

Amsterdam, Netherlands

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06413667