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Completed

NCT Number: NCT02692937

Is Chronic Whiplash-associated Pain of Neurogenic Origin?

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).

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Key information

Age range

20 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Department of Neurosurgery, Skåne University Hospital

Lund, Skåne County, 22185, Sweden

About this study

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).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Neurolysis

Procedure

Traditional neck-specific exercise program

Other

Primary outcomes

  1. The Neck Disability Index (NDI)

    Time frame: 24 months

    Questionnaire

Secondary outcomes

  1. The Symptom index

    Time frame: 24 months

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

  2. Self-Efficacy Scale (SES)

    Time frame: 24 months

    Questionnaire

  3. Headache Disability Index (HDI)

    Time frame: 24 months

    Questionnaire

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

    Time frame: 24 months

    Questionnaire

  5. Zung Self-Rating Depression Scale (Zung)

    Time frame: 24 months

    Questionnaire

  6. Modified Somatic Perception Questionnaire (MSPQ)

    Time frame: 24 months

    Questionnaire

  7. EuroQol questionnaire (EQ-5D)

    Time frame: 24 months

    Questionnaire

  8. EuroQol thermometer (EQ-VAS)

    Time frame: 24 months

    Questionnaire

  9. Cervical range of motion (CROM)

    Time frame: 12 months

  10. Pain drawing, perceived face and body sensations

    Time frame: 12 months

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

  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.

    Time frame: 12 months

    The physiotherapist palpates each trigger point, according to a detailed protocol developed for the present study.

Sponsors and collaborators

Lead sponsor

Region Skane

Other

Collaborators

  • Lund University

Registry information

Official study 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

Important dates

Study start
2011
Primary completion
2017
Study completion
2017
First posted
Feb 26, 2016
Registry last updated
Apr 7, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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