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Is Chronic Whiplash-associated Pain of Neurogenic Origin?

Primary Purpose

Whiplash Injuries

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Neurolysis
Traditional neck-specific exercise program
Sponsored by
Region Skane
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Whiplash Injuries focused on measuring Neurosurgical Procedures, Nerve Block, Exercise therapy, Physical Therapy Specialty

Eligibility Criteria

20 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • trauma that has caused a whiplash injury
  • at least one year of incapacitating chronic neck pain/headache related to the injury (WAD II-III)
  • typical trigger points in the back of the head or in the neck and significant pain relief with local anesthesia towards the painful areas

Exclusion Criteria:

  • mental illness
  • abuse of drugs/alcohol
  • not understanding or reading the Swedish language
  • previous surgery in the back of the head

Sites / Locations

  • The Department of Neurosurgery, Skåne University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Surgery and exercise

Exercise, Active Comparator

Arm Description

Neurolysis of peripheral nerves in the back of the head and/or neck. Traditional neck-specific exercise program including five individual treatments sessions within 3 months plus home program over 9 months.

Traditional neck-specific exercise program including five individual treatments sessions within 3 months plus home program over 9 months.

Outcomes

Primary Outcome Measures

The Neck Disability Index (NDI)
Questionnaire

Secondary Outcome Measures

The Symptom index
Related symptoms (pain) psychosomatic aspects and any disability due to the neck complaint. Questionnaire.
Self-Efficacy Scale (SES)
Questionnaire
Headache Disability Index (HDI)
Questionnaire
Whiplash Associated Disorders - Disability Index (WAD-DI)
Questionnaire
Zung Self-Rating Depression Scale (Zung)
Questionnaire
Modified Somatic Perception Questionnaire (MSPQ)
Questionnaire
EuroQol questionnaire (EQ-5D)
Questionnaire
EuroQol thermometer (EQ-VAS)
Questionnaire
Cervical range of motion (CROM)
Pain drawing, perceived face and body sensations
The characteristics of the patients sensations/pain are described on two different charts.
Exploratory outcome. Perceived pain on a Numeric Rating Scale (NRS) for 14 specific trigger points in the muscles of the occipital region, neck and shoulder.
The physiotherapist palpates each trigger point, according to a detailed protocol developed for the present study.

Full Information

First Posted
February 15, 2016
Last Updated
April 3, 2020
Sponsor
Region Skane
Collaborators
Lund University
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1. Study Identification

Unique Protocol Identification Number
NCT02692937
Brief Title
Is Chronic Whiplash-associated Pain of Neurogenic Origin?
Official Title
Is Chronic Whiplash-associated Pain of Neurogenic Origin? A Study Protocol of a Randomized Controlled Trial Comparing Neurolysis of Peripheral Nerves With Traditional Neck-specific Exercise
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
March 2017 (Actual)
Study Completion Date
September 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Region Skane
Collaborators
Lund University

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to compare the effects of neurolysis with the effects of a exercise program on pain and other symptoms in individuals with chronic whiplash (WAD II-III).
Detailed Description
People with whiplash associated disorders (WAD) grade II-III have chronic severe pain and symptoms and reduced quality of life. The origin of the symptoms is still unknown, and there are to date no available guidelines for treatment of this condition. The lack of effective treatment leads to high costs for the patients, and to society, due to considerable medical care and work loss. After providing a written consent, the patients will be randomized to either surgical treatment with neurolysis of peripheral nerve/s in the back of the head and/or neck plus physiotherapy or to physiotherapy (care-as-usual) only. Both groups will be treated with the same traditional neck-specific exercise program for 12 months. All participants will be evaluated with patient-reported outcomes and clinical examination at baseline, and at 6, 12 and 24 months after inclusion. The main outcome will be change in NDI from baseline to the 2-year follow-up. A preliminary sample-size calculation shows that 27 patients are needed for each treatment arm to detect a clinically important change of 10 points in NDI, with a between-group standard deviation of 13 point (statistical power of 80 % and a 5% significance level). To account for a 20% drop-out rate, 32 patients will be included per arm. Because this is the first RCT on neurolysis vs care-as-usual treatment, a second sample-size calculation including empirical data will performed by an independent statistician, without breaking the code, when 30 patients in each group have been included. Secondary outcomes include VAS (average pain including pain in the head, neck and face), symptom index, self-efficacy, HDI, WAD-DI, psychosomatic aspects, quality of life and clinical examination. Data will be performed with parametric, or non-parametric statistics, as appropriate, in IBM SPSS Statistics version 22 for Mac (IBM Corp., Armonk, NY, USA). Analysis will be performed according to both intention-to-treat and per protocol. To account for missing data, the previous group means value will be considered to remain form the last occasion and used as carry forward. For continuous data, differences in mean change (baseline vs follow-up) will be compared between groups and adjusted in relation to baseline values. For categorical data, differences in median change (baseline vs follow-up) will be compared between groups and adjusted in relation to baseline values. Effect sizes will be calculated for all measures. This Randomized Controlled Study is approved and funded by the National Board of Health and Welfare in Sweden (project no 6168/2007).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Whiplash Injuries
Keywords
Neurosurgical Procedures, Nerve Block, Exercise therapy, Physical Therapy Specialty

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Surgery and exercise
Arm Type
Experimental
Arm Description
Neurolysis of peripheral nerves in the back of the head and/or neck. Traditional neck-specific exercise program including five individual treatments sessions within 3 months plus home program over 9 months.
Arm Title
Exercise, Active Comparator
Arm Type
Active Comparator
Arm Description
Traditional neck-specific exercise program including five individual treatments sessions within 3 months plus home program over 9 months.
Intervention Type
Procedure
Intervention Name(s)
Neurolysis
Intervention Type
Other
Intervention Name(s)
Traditional neck-specific exercise program
Primary Outcome Measure Information:
Title
The Neck Disability Index (NDI)
Description
Questionnaire
Time Frame
24 months
Secondary Outcome Measure Information:
Title
The Symptom index
Description
Related symptoms (pain) psychosomatic aspects and any disability due to the neck complaint. Questionnaire.
Time Frame
24 months
Title
Self-Efficacy Scale (SES)
Description
Questionnaire
Time Frame
24 months
Title
Headache Disability Index (HDI)
Description
Questionnaire
Time Frame
24 months
Title
Whiplash Associated Disorders - Disability Index (WAD-DI)
Description
Questionnaire
Time Frame
24 months
Title
Zung Self-Rating Depression Scale (Zung)
Description
Questionnaire
Time Frame
24 months
Title
Modified Somatic Perception Questionnaire (MSPQ)
Description
Questionnaire
Time Frame
24 months
Title
EuroQol questionnaire (EQ-5D)
Description
Questionnaire
Time Frame
24 months
Title
EuroQol thermometer (EQ-VAS)
Description
Questionnaire
Time Frame
24 months
Title
Cervical range of motion (CROM)
Time Frame
12 months
Title
Pain drawing, perceived face and body sensations
Description
The characteristics of the patients sensations/pain are described on two different charts.
Time Frame
12 months
Title
Exploratory outcome. Perceived pain on a Numeric Rating Scale (NRS) for 14 specific trigger points in the muscles of the occipital region, neck and shoulder.
Description
The physiotherapist palpates each trigger point, according to a detailed protocol developed for the present study.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: trauma that has caused a whiplash injury at least one year of incapacitating chronic neck pain/headache related to the injury (WAD II-III) typical trigger points in the back of the head or in the neck and significant pain relief with local anesthesia towards the painful areas Exclusion Criteria: mental illness abuse of drugs/alcohol not understanding or reading the Swedish language previous surgery in the back of the head
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leif Anderberg, MD, PhD
Organizational Affiliation
The Department of Neurosurgery, Skåne University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Department of Neurosurgery, Skåne University Hospital
City
Lund
State/Province
Skåne
ZIP/Postal Code
22185
Country
Sweden

12. IPD Sharing Statement

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