Central Sensitization in Chronic Whiplash Patients
- Conditions
- Chronic Pain
- Interventions
- Radiation: SpectroscopyOther: QuestionnairesProcedure: 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
- Whiplash syndrome
- Chronic pain
- Age between 18 to 65 years
- 4 months to 2 years after the whiplash syndrome
- Neurological disease
- Claustrophobia
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Non-injured Conditioned Pain Modulation Subjects without whiplash syndrome. The inclusion criteria are defined as a absence of previous or actual symptoms or signs of neck pain. Whiplash-no Pain Questionnaires Subjects 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-injured Spectroscopy Subjects without whiplash syndrome. The inclusion criteria are defined as a absence of previous or actual symptoms or signs of neck pain. Whiplash-Pain Conditioned Pain Modulation Subjects 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-Pain Spectroscopy Subjects 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-Pain Questionnaires Subjects 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 Pain Spectroscopy Subjects 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 Pain Conditioned Pain Modulation Subjects 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-injured Questionnaires Subjects without whiplash syndrome. The inclusion criteria are defined as a absence of previous or actual symptoms or signs of neck pain.
- Primary Outcome Measures
Name Time Method Conditioned Pain Modulation Baseline at 0 min Conditioned Pain Modulation will be measured by a Pathway system (Medoc Ltd)
Metabolite concentrations Baseline at 0 min The metabolite concentrations will be measured by magnetic resonance (spectroscopy)
Brief Pain Inventory Baseline 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 Inventory Baseline at 0 min Neurophatic Pain Symptoms Inventory (NPSI), it is used to detect paresthesia/dysaesthesia, evoked pain and paroxysmal pain.
Pain Catastrophizing Helplessness Subscale Baseline at 0 min Pain Catastrophizing Helplessness Subscale it is used to assess the catastrophizing score
Neck Disability Index Baseline at 0 min Neck Disability Index (NDI), it is used to assess the disability after whiplash syndrome
- Secondary Outcome Measures
Name Time Method