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CompletedNCT02692937Updated Apr 7, 2020

Is Chronic Whiplash-associated Pain of Neurogenic Origin?

An interventional study of Neurolysis and Traditional neck-specific exercise program in Whiplash Injuries, sponsored by Region Skane. Completed at 1 site in Sweden. Open to participants aged 20 Years to 60 Years. Per ClinicalTrials.gov, last updated 2020-04-07.

Sponsored by Region Skane · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
20 Years to 60 Years
Sex
All
01

Study 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).

Read the 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).

02

Conditions studied

  • Whiplash Injuries

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Keywords

  • Neurosurgical Procedures
  • Nerve Block
  • Exercise therapy
  • Physical Therapy Specialty
03

In context

Whiplash Injuries

68 studies on the registry are indexed under Whiplash Injuries; 8 are open to participants now.

This study's enrollment of 60 is below the median of 68 across 49 interventional studies indexed under Whiplash Injuries.

Browse Whiplash Injuries studies →

Lead sponsor

Region Skane is the lead sponsor of 372 studies on the registry; 113 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

Exclusion Criteria:

  • mental illness
  • abuse of drugs/alcohol
  • not understanding or reading the Swedish language
  • previous surgery in the back of the head
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    Surgery and exercise

    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.

    Procedure: Neurolysis · Other: Traditional neck-specific exercise program

  • Active comparator
    Exercise, Active Comparator

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

    Other: Traditional neck-specific exercise program

Interventions

  • ProcedureNeurolysis
  • OtherTraditional neck-specific exercise program
06

What researchers measure

Primary outcomes

  1. The Neck Disability Index (NDI)

    Questionnaire

    Time frame: 24 months

Secondary outcomes

  1. The Symptom index

    Related symptoms (pain) psychosomatic aspects and any disability due to the neck complaint. Questionnaire.

    Time frame: 24 months

  2. Self-Efficacy Scale (SES)

    Questionnaire

    Time frame: 24 months

  3. Headache Disability Index (HDI)

    Questionnaire

    Time frame: 24 months

  4. Whiplash Associated Disorders - Disability Index (WAD-DI)

    Questionnaire

    Time frame: 24 months

  5. Zung Self-Rating Depression Scale (Zung)

    Questionnaire

    Time frame: 24 months

  6. Modified Somatic Perception Questionnaire (MSPQ)

    Questionnaire

    Time frame: 24 months

  7. EuroQol questionnaire (EQ-5D)

    Questionnaire

    Time frame: 24 months

  8. EuroQol thermometer (EQ-VAS)

    Questionnaire

    Time frame: 24 months

  9. Cervical range of motion (CROM)

    Time frame: 12 months

  10. Pain drawing, perceived face and body sensations

    The characteristics of the patients sensations/pain are described on two different charts.

    Time frame: 12 months

  11. 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.

    Time frame: 12 months

07

Study locations

1 site
  • The Department of Neurosurgery, Skåne University Hospital
    Lund, Skåne 22185, Sweden
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 7, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02692937
Lead sponsor
Region Skane
Collaborators
Lund University
Responsible party
Sponsor
First posted
Feb 26, 2016
Start date
Jan 2011
Primary completion
Mar 2017
Completion
Sep 2017
Last update
Apr 7, 2020

Study contacts

Leif Anderberg, MD, PhD
principal investigator · The Department of Neurosurgery, Skåne University Hospital
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2020. You cannot join it, but the record below documents what was studied.

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