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Central Sensitization in Chronic Whiplash Patients

Conditions
Chronic Pain
Interventions
Radiation: Spectroscopy
Other: Questionnaires
Procedure: Conditioned Pain Modulation
Registration Number
NCT03005691
Lead Sponsor
University of Castilla-La Mancha
Brief Summary

The purpose of this study is to determine whether the metabolite concentrations within the anterior cingulate cortex and periaqueductal gray matter predict the intensity and interference of neuropathic pain after the development of chronic whiplash syndrome.

Detailed Description

Persistent chronic pain is a common symptom of whiplash leading to reduced quality of life. Little information is available regarding changes in brain processing areas and change in central sensitization to noxious input during the chronic phase of whiplash. Metabolite concentrations in the anterior cingulate cortex and periaqueductal gray matter may be predictors of neuropathic pain and these changes may explain the development of central sensitization in people with chronic whiplash.

Until now, there is not any study that show this approach.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Whiplash syndrome
  • Chronic pain
  • Age between 18 to 65 years
  • 4 months to 2 years after the whiplash syndrome
Exclusion Criteria
  • Neurological disease
  • Claustrophobia

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Non-injuredConditioned Pain ModulationSubjects without whiplash syndrome. The inclusion criteria are defined as a absence of previous or actual symptoms or signs of neck pain.
Whiplash-no PainQuestionnairesSubjects with chronic whiplash syndrome and pain. The inclusion criteria for pain include the ausence of daily pain during the previous 8 weeks. Specifically, pain will be diagnosed based on the pain intensity measured on the 0 to 10 numerical rating scale. The maximun will be 2 points. Subjects will be recruited between the 4 months until 2 years after the whiplash.
Non-injuredSpectroscopySubjects without whiplash syndrome. The inclusion criteria are defined as a absence of previous or actual symptoms or signs of neck pain.
Whiplash-PainConditioned Pain ModulationSubjects with chronic whiplash syndrome and pain. The inclusion criteria for pain include the presence of daily pain during the previous 8 weeks. Specifically, pain will be diagnosed based on the pain intensity measured on the 0 to 10 numerical rating scale. The minimum will be 2 points. Subjects will be recruited between the 4 months until 2 years after the whiplash.
Whiplash-PainSpectroscopySubjects with chronic whiplash syndrome and pain. The inclusion criteria for pain include the presence of daily pain during the previous 8 weeks. Specifically, pain will be diagnosed based on the pain intensity measured on the 0 to 10 numerical rating scale. The minimum will be 2 points. Subjects will be recruited between the 4 months until 2 years after the whiplash.
Whiplash-PainQuestionnairesSubjects with chronic whiplash syndrome and pain. The inclusion criteria for pain include the presence of daily pain during the previous 8 weeks. Specifically, pain will be diagnosed based on the pain intensity measured on the 0 to 10 numerical rating scale. The minimum will be 2 points. Subjects will be recruited between the 4 months until 2 years after the whiplash.
Whiplash-no PainSpectroscopySubjects with chronic whiplash syndrome and pain. The inclusion criteria for pain include the ausence of daily pain during the previous 8 weeks. Specifically, pain will be diagnosed based on the pain intensity measured on the 0 to 10 numerical rating scale. The maximun will be 2 points. Subjects will be recruited between the 4 months until 2 years after the whiplash.
Whiplash-no PainConditioned Pain ModulationSubjects with chronic whiplash syndrome and pain. The inclusion criteria for pain include the ausence of daily pain during the previous 8 weeks. Specifically, pain will be diagnosed based on the pain intensity measured on the 0 to 10 numerical rating scale. The maximun will be 2 points. Subjects will be recruited between the 4 months until 2 years after the whiplash.
Non-injuredQuestionnairesSubjects without whiplash syndrome. The inclusion criteria are defined as a absence of previous or actual symptoms or signs of neck pain.
Primary Outcome Measures
NameTimeMethod
Conditioned Pain ModulationBaseline at 0 min

Conditioned Pain Modulation will be measured by a Pathway system (Medoc Ltd)

Metabolite concentrationsBaseline at 0 min

The metabolite concentrations will be measured by magnetic resonance (spectroscopy)

Brief Pain InventoryBaseline at 0 min

Brief Pain Inventory (BPI), it is used to evaluate the subject's perception of pain severity and its interference.

Neurophatic Pain Symptoms InventoryBaseline at 0 min

Neurophatic Pain Symptoms Inventory (NPSI), it is used to detect paresthesia/dysaesthesia, evoked pain and paroxysmal pain.

Pain Catastrophizing Helplessness SubscaleBaseline at 0 min

Pain Catastrophizing Helplessness Subscale it is used to assess the catastrophizing score

Neck Disability IndexBaseline at 0 min

Neck Disability Index (NDI), it is used to assess the disability after whiplash syndrome

Secondary Outcome Measures
NameTimeMethod
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