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Modern Pain Neuroscience Applied to Chronic Pain in Patients With Chronic Whiplash Associated Disorders

Primary Purpose

Whiplash

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Modern pain neuroscience approach
Usual care evidence-based physiotherapy
Sponsored by
Vrije Universiteit Brussel
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Whiplash focused on measuring chronic whiplash associated disorders, central sensitization, electroencephalography, physiotherapy, chronic pain, functionality, quality of life, stress management, randomized controlled trial, modern neuroscience approach, pain neuroscience education, neck school, exercise therapy, pain cognitions

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Experienced a whiplash trauma which is at least 3 months old and causes pain since at least 3 months, with pain experience with a mean pain frequency of 3 or more days per week, and with self-reported moderate to severe pain-related disability, established by a score of 15 or more of a maximum of 50 on the Neck Disability Index
  • Patients classified as WAD II or WAD III on the modified Quebec Task Force Scale
  • Native Dutch speaker
  • Not starting new treatments or medication and continuing their usual care 6 weeks prior to and during study participation (to obtain a steady state)
  • Refraining from non-opioid analgesics in the previous 48h of the assessments
  • Refraining from caffeine, alcohol, and nicotine in the previous 24h of the assessments

Exclusion Criteria:

  • Neuropathic pain
  • Being pregnant or having given birth in the preceding year
  • Chronic fatigue syndrome
  • Fibromyalgia
  • Cardiovascular disorders
  • Epilepsy
  • Endocrinological disorders
  • Rheumatic disorders
  • Psychiatric disorders
  • History of neck surgery
  • Loss of consciousness during/after the whiplash trauma
  • Post-traumatic amnesia

Sites / Locations

  • Sint-jozefkliniek Campus Bornem (AZ Rivierenland)
  • Ghent University
  • Vrije Universiteit Brussel

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Modern pain neuroscience approach

Usual care evidence-based physiotherapy

Arm Description

Modern pain neuroscience approach

Usual care physiotherapy

Outcomes

Primary Outcome Measures

Self-reported functional status or disability
The Dutch version of the Neck Disability Index (questionnaire)

Secondary Outcome Measures

Self-reported functional status or disability
The Dutch version of the Neck Disability Index (questionnaire)
Self-reported health-related quality of life
The Dutch version of the Short Form Health Survey-36 items (questionnaire)
Self-reported pain assessment
A 0-10 Numeric Rating Scale for pain (questionnaire). Patients fill out the Numeric Rating Scale (0 no pain - 10 worst pain imaginable) for their perceived neck pain.
Self-reported central sensitization symptoms
The Dutch version of the Central Sensitization Inventory (questionnaire)
Electrical detection and electrical pain thresholds with a constant current electrical stimulator (DS7A Digitimer)
Determination of the electrical detection and electrical pain threshold with the electrical stimulator will be performed at the sural nerve of the dominant leg and at the median nerve of the dominant arm.
Endogenous pain facilitation assessed by a temporal summation paradigm
Temporal summation of electrical pain will be assessed by delivering 20 electrical stimuli at the intensity of the electrical pain threshold.
Endogenous pain inhibition assessed by a conditioned pain modulation paradigm
Conditioned pain modulation will be tested with electrical stimulation as test stimulus and the cold pressor test (immersion the hand up to the wrist in cold water of 12°C) as conditioning stimulus.
Quantitative Electroencephalography (QEEG) (Sienna digital EEG, EMS Biomedical, Korneuburg, Austria) will be recorded from 32 Sn surface electrodes using an electrode cap (Headcap, Expertise in Medical Solutions Biomedical, Korneuburg, Austria).
During the condition pain modulation paradigm a QEEG will be administered to examine various brain activity parameters.
Self-reported psychological correlates: Pain catastrophizing
The Dutch version of the Pain Catastrophizing Scale (questionnaire)
Self-reported psychological correlates: Illness perceptions
The Dutch version of the illness perception questionnaire-revised (questionnaire)
Self-reported psychological correlates: Post-traumatic stress
The Dutch version of the Impact of Event Scale revised (questionnaire)
Self-reported psychological correlates: Pain-related fear and fear-avoidance behaviour
The Dutch version of the Pain anxiety symptoms scale (PASS-20) (questionnaire)
Socio-economic factors
Self-reported questionnaire and data including health-care expenditure from publicly funded healthcare organizations.

Full Information

First Posted
August 1, 2017
Last Updated
November 24, 2022
Sponsor
Vrije Universiteit Brussel
Collaborators
University Hospital, Ghent, University Ghent, Research Foundation Flanders, Universitair Ziekenhuis Brussel
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1. Study Identification

Unique Protocol Identification Number
NCT03239938
Brief Title
Modern Pain Neuroscience Applied to Chronic Pain in Patients With Chronic Whiplash Associated Disorders
Official Title
Contemporary Pain Neuroscience Compared to Usual Care Evidence-based Physiotherapy Applied to Chronic Pain in Patients With Chronic Whiplash Associated Disorders: Can we Decrease Central Sensitization?
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
August 17, 2017 (Actual)
Primary Completion Date
June 13, 2022 (Actual)
Study Completion Date
June 13, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vrije Universiteit Brussel
Collaborators
University Hospital, Ghent, University Ghent, Research Foundation Flanders, Universitair Ziekenhuis Brussel

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Modern pain neuroscience has advanced our understanding of chronic whiplash associated disorders (WAD). Previous studies have shown the importance of central sensitization, characterized by hypersensitivity of the somatosensory system, in explaining poor treatment outcome. Therefore, and to address the need for a better treatment of chronic WAD, we recently proposed a modern neuroscience approach to chronic WAD. Such approach includes two specific parts: therapeutic pain neuroscience education followed by dynamic and functional cognition-targeted exercise therapy and stress management techniques. The primary scientific objective of the study entails examining the effectiveness of a modern neuroscience approach versus usual care evidence-based physiotherapy for reducing dysfunctioning in patients with chronic WAD. The secondary scientific objective of the study entails examining the effectiveness of a modern neuroscience approach versus usual care evidence-based physiotherapy for reducing pain, central sensitization, psychosocial problems, and socio-economic burden in patients with chronic WAD. The trial will randomize 120 patients with chronic WAD, aged between 18 and 65 years, to the experimental (modern pain neuroscience approach including 3 sessions of therapeutic pain neuroscience education followed by 15 sessions of dynamic and functional cognition-targeted exercise therapy and stress management techniques (n = 60)) or the control treatment (usual care physiotherapy including 3 sessions of neck school followed by 15 sessions of graded and active exercise therapy focusing on strength, flexibility, endurance, and ergonomic principles (n= 60)). The primary outcome measure is self-reported functional status. Secondary outcome measures include pain, health-related quality of life, psychological correlates, measures of central sensitization, and socio-economic factors. In addition, quantitative scalp Electroencephalography (EEG) to measure various parameters of brain activation will be performed during a conditioned pain modulation paradigm. Baseline assessment of all outcome measures will be performed. Follow-up assessments will be performed immediately after 16 weeks of therapy (all tests), and 6 months (all tests) and 12 months (only questionnaires) after finishing the therapeutic intervention. To investigate these objectives, a multi-center triple-blind randomized, controlled trial with 1 year follow up will be performed.
Detailed Description
Modern pain neuroscience has advanced our understanding of chronic whiplash associated disorders (WAD). Previous studies have shown the importance of central sensitization, characterized by hypersensitivity of the somatosensory system, in explaining poor treatment outcome. Therefore, and to address the need for a better treatment of chronic WAD, we recently proposed a modern neuroscience approach to chronic WAD. Such approach includes two specific parts: 3 sessions of therapeutic pain neuroscience education followed by 15 sessions of dynamic and functional cognition-targeted exercise therapy and stress management techniques. The main principles of cognition-targeted are the following: All exercises should be performed in a time-contingent ("Perform this exercise 10 times, regardless of the pain") rather than in a symptom-contingent way ("Stop or adjust the exercise when it hurts"). Goal setting is essentially done together with the patient, focussing on functionality. The treating physical therapist should continuously assess and challenge the patients' cognitions and perceptions about the pain and the anticipated outcome of each exercise, to change maladaptive cognitions and perceptions into positive ones. The primary scientific objective of the study entails examining the effectiveness of a modern pain neuroscience approach versus usual care evidence-based physiotherapy for reducing dysfunctioning in patients with chronic WAD. The secondary scientific objective of the study entails examining the effectiveness of a modern neuroscience approach versus usual care evidence-based physiotherapy for reducing pain, central sensitization, psychological problems, and socio-economic burden in patients with chronic WAD. The trial will randomize 120 patients with chronic WAD, aged between 18 and 65 years, to the experimental (modern pain neuroscience approach (n = 60)) or control treatment (usual care evidence-based physiotherapy: 3 sessions of neck school followed by 15 sessions of graded and active exercise therapy focusing on strength, flexibility, endurance, and ergonomic principles (n= 60)). The primary outcome measure is functional status. Secondary outcome measures include pain, health-related quality of life, psychological correlates, socio-economic factors, and measures of central sensitization, including electrical detection and electrical pain thresholds measured with a constant current electrical stimulator, endogenous pain facilitation (temporal summation of electrical pain), endogenous pain inhibition assessed by the conditioned pain modulation paradigm (electrical stimulation as test stimulus and the cold pressor test (immersion of one hand in cold water of 12°C) as conditioning stimulus). In addition, quantitative scalp Electroencephalography (EEG) to measure various parameters of brain activation will be performed during the conditioned pain modulation paradigm. To comply with these scientific objectives, the 120 chronic WAD patients will be subjected to the baseline assessment of all outcome measures. Follow-up assessments will be performed immediately after 16 weeks of therapy (all tests), and 6 months (all tests) and 12 months (only questionnaires) after finishing the therapeutic intervention. To investigate these objectives, a muli-center triple-blind randomized, controlled trial with 1 year follow up will be performed. Appropriate statistical analyses will be performed to evaluate and compare treatment effects. Statistical, as well as clinical significant differences will be defined and the effect size will be determined. Relations between functional status, pain, psychological correlates and central sensitization will be investigated. Furthermore, prediction of pain and functional status by central sensitization and psychological correlates will be performed in chronic WAD patients. Also, factors associated with clinically important changes in the outcome measures will be unraveled. In addition, factors associated with poor outcome following treatment will be assessed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Whiplash
Keywords
chronic whiplash associated disorders, central sensitization, electroencephalography, physiotherapy, chronic pain, functionality, quality of life, stress management, randomized controlled trial, modern neuroscience approach, pain neuroscience education, neck school, exercise therapy, pain cognitions

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The trial will randomize 120 patients with chronic WAD, aged between 18 and 65 years, to the experimental (modern neuroscience approach including 3 sessions of therapeutic pain neuroscience education followed by 15 sessions of dynamic and functional cognition-targeted exercise therapy and stress management techniques (n = 60)) or the control treatment (usual care physiotherapy: 3 sessions of neck school followed by 15 sessions of exercise therapy focusing on strength, flexibility, endurance, and ergonomic principles (n= 60)).
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Modern pain neuroscience approach
Arm Type
Experimental
Arm Description
Modern pain neuroscience approach
Arm Title
Usual care evidence-based physiotherapy
Arm Type
Active Comparator
Arm Description
Usual care physiotherapy
Intervention Type
Behavioral
Intervention Name(s)
Modern pain neuroscience approach
Intervention Description
The modern pain neuroscience approach includes 3 sessions (1 group and 2 individual sessions) of therapeutic pain neuroscience education followed by 15 individual sessions of dynamic and functional cognition-targeted exercise therapy and stress management techniques. In addition, participants will be instructed to perform a daily set of home exercises. The exercises will be performed in a time-contingent way. The 18 sessions will be spread over a period of 16 weeks.
Intervention Type
Behavioral
Intervention Name(s)
Usual care evidence-based physiotherapy
Intervention Description
The usual care evidence-based physiotherapy includes 3 sessions (1 group and 2 individual sessions) of neck school followed by 15 individual sessions of graded and active exercise therapy focusing on strength, flexibility, endurance, and ergonomic principles. In addition, participants will be instructed to perform a daily set of home exercises. The exercises will be performed in a symptom-contingent way. The 18 sessions will be spread over a period of 16 weeks.
Primary Outcome Measure Information:
Title
Self-reported functional status or disability
Description
The Dutch version of the Neck Disability Index (questionnaire)
Time Frame
The change between the baseline assessment and the 6 months follow-up assessment (6 months after the end of the therapy)
Secondary Outcome Measure Information:
Title
Self-reported functional status or disability
Description
The Dutch version of the Neck Disability Index (questionnaire)
Time Frame
Baseline assessment, T1 follow-up assessment after 16 weeks of therapy, T3 follow-up assessment 12 months after the end of the therapy.
Title
Self-reported health-related quality of life
Description
The Dutch version of the Short Form Health Survey-36 items (questionnaire)
Time Frame
Baseline assessment, T1 follow-up assessment after 16 weeks of therapy, T2 follow-up assessment 6 months after the end of the therapy, T3 assessment 12 months after the end of the therapy.
Title
Self-reported pain assessment
Description
A 0-10 Numeric Rating Scale for pain (questionnaire). Patients fill out the Numeric Rating Scale (0 no pain - 10 worst pain imaginable) for their perceived neck pain.
Time Frame
Baseline assessment, T1 follow-up assessment after 16 weeks of therapy, T2 follow-up assessment 6 months after the end of the therapy, T3 follow-up assessment 12 months after the end of the therapy.
Title
Self-reported central sensitization symptoms
Description
The Dutch version of the Central Sensitization Inventory (questionnaire)
Time Frame
Baseline assessment, T1 follow-up assessment after 16 weeks of therapy, T2 follow-up assessment 6 months after the end of the therapy, T3 follow-up assessment 12 months after the end of the therapy.
Title
Electrical detection and electrical pain thresholds with a constant current electrical stimulator (DS7A Digitimer)
Description
Determination of the electrical detection and electrical pain threshold with the electrical stimulator will be performed at the sural nerve of the dominant leg and at the median nerve of the dominant arm.
Time Frame
Baseline assessment, T1 follow-up assessment after 16 weeks of therapy, T2 follow-up assessment 6 months after the end of the therapy
Title
Endogenous pain facilitation assessed by a temporal summation paradigm
Description
Temporal summation of electrical pain will be assessed by delivering 20 electrical stimuli at the intensity of the electrical pain threshold.
Time Frame
Baseline assessment, T1 follow-up assessment after 16 weeks of therapy, T2 follow-up assessment 6 months after the end of the therapy
Title
Endogenous pain inhibition assessed by a conditioned pain modulation paradigm
Description
Conditioned pain modulation will be tested with electrical stimulation as test stimulus and the cold pressor test (immersion the hand up to the wrist in cold water of 12°C) as conditioning stimulus.
Time Frame
Baseline assessment, T1 follow-up assessment after 16 weeks of therapy, T2 follow-up assessment 6 months after the end of the therapy
Title
Quantitative Electroencephalography (QEEG) (Sienna digital EEG, EMS Biomedical, Korneuburg, Austria) will be recorded from 32 Sn surface electrodes using an electrode cap (Headcap, Expertise in Medical Solutions Biomedical, Korneuburg, Austria).
Description
During the condition pain modulation paradigm a QEEG will be administered to examine various brain activity parameters.
Time Frame
Baseline assessment, T1 follow-up assessment after 16 weeks of therapy, T2 follow-up assessment 6 months after the end of the therapy
Title
Self-reported psychological correlates: Pain catastrophizing
Description
The Dutch version of the Pain Catastrophizing Scale (questionnaire)
Time Frame
Baseline assessment, T1 follow-up assessment after 16 weeks of therapy, T2 follow-up assessment 6 months after the end of the therapy, T3 follow-up assessment 12 months after the end of the therapy.
Title
Self-reported psychological correlates: Illness perceptions
Description
The Dutch version of the illness perception questionnaire-revised (questionnaire)
Time Frame
Baseline assessment, T1 follow-up assessment after 16 weeks of therapy, T2 follow-up assessment 6 months after the end of the therapy, T3 follow-up assessment 12 months after the end of the therapy.
Title
Self-reported psychological correlates: Post-traumatic stress
Description
The Dutch version of the Impact of Event Scale revised (questionnaire)
Time Frame
Baseline assessment, T1 follow-up assessment after 16 weeks of therapy, T2 follow-up assessment 6 months after the end of the therapy, T3 follow-up assessment 12 months after the end of the therapy.
Title
Self-reported psychological correlates: Pain-related fear and fear-avoidance behaviour
Description
The Dutch version of the Pain anxiety symptoms scale (PASS-20) (questionnaire)
Time Frame
Baseline assessment, T1 follow-up assessment after 16 weeks of therapy, T2 follow-up assessment 6 months after the end of the therapy, T3 follow-up assessment 12 months after the end of the therapy.
Title
Socio-economic factors
Description
Self-reported questionnaire and data including health-care expenditure from publicly funded healthcare organizations.
Time Frame
Baseline assessment, T2 follow-up assessment 6 months after the end of the therapy, T3 follow-up assessment 12 months after the end of the therapy, 1 year before enrollment in the study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Experienced a whiplash trauma which is at least 3 months old and causes pain since at least 3 months, with pain experience with a mean pain frequency of 3 or more days per week, and with self-reported moderate to severe pain-related disability, established by a score of 15 or more of a maximum of 50 on the Neck Disability Index Patients classified as WAD II or WAD III on the modified Quebec Task Force Scale Native Dutch speaker Not starting new treatments or medication and continuing their usual care 6 weeks prior to and during study participation (to obtain a steady state) Refraining from non-opioid analgesics in the previous 48h of the assessments Refraining from caffeine, alcohol, and nicotine in the previous 24h of the assessments Exclusion Criteria: Neuropathic pain Being pregnant or having given birth in the preceding year Chronic fatigue syndrome Fibromyalgia Cardiovascular disorders Epilepsy Endocrinological disorders Rheumatic disorders Psychiatric disorders History of neck surgery Loss of consciousness during/after the whiplash trauma Post-traumatic amnesia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Iris Coppieters, PhD
Organizational Affiliation
Vrije Universiteit Brussel
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Jo Nijs, PhD
Organizational Affiliation
Vrije Universiteit Brussel
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sint-jozefkliniek Campus Bornem (AZ Rivierenland)
City
Bornem
State/Province
Antwerpen
ZIP/Postal Code
2880
Country
Belgium
Facility Name
Ghent University
City
Ghent
State/Province
Oost-Vlaanderen
ZIP/Postal Code
9000
Country
Belgium
Facility Name
Vrije Universiteit Brussel
City
Brussels
ZIP/Postal Code
1000
Country
Belgium

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
24703832
Citation
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PubMed Identifier
23008191
Citation
Van Oosterwijck J, Nijs J, Meeus M, Paul L. Evidence for central sensitization in chronic whiplash: a systematic literature review. Eur J Pain. 2013 Mar;17(3):299-312. doi: 10.1002/j.1532-2149.2012.00193.x. Epub 2012 Sep 25.
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Citation
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Modern Pain Neuroscience Applied to Chronic Pain in Patients With Chronic Whiplash Associated Disorders

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