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CompletedNCT03040245WHIPLASHUpdated Feb 2, 2017

Measuring the Impact of the French Version of the Whiplash Book

An observational study in Whiplash Trauma, sponsored by University Hospital, Clermont-Ferrand. Completed at 1 site in France. Open to participants aged 25 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-02-02.

Sponsored by University Hospital, Clermont-Ferrand · Observational

Study type
Observational
Model
Other
Time perspective
Other
Enrollment
95
Ages
25 Years to 65 Years
Sex
All
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Study summary

Whiplash trauma and the resulting whiplash associated disorders have been the subject of much attention in the scientific literature and remain a major public health problem.

The most commonly encountered symptoms are neck pain, headache, low back pain, shoulder pain, as well as visual impairment. It is not unusual for neck pain to become chronic, and when this occurs, there may be serious consequences on a social, professional and financial level.

Even though the role of the initial episode should not be ignored, progression to chronic pain is probably multifactorial and, like non-specific low back pain, psycho-social factors, and in particular patient fears and belief, seem to play a relevant role, as do environmental factors. The professional consensus is that it is useful to provide targeted information at an early stage in whiplash settings in order to reduce mistaken fears and beliefs. A preliminary study enabled the investigators to validate a French version of an information booklet that draws on validated data from evidence-based medicine. The booklet was "Le guide du coup de fouet cervical," the French version of The Whiplash Book. This study showed that fears and beliefs were considerably high in a population without neck problems who were working in hospitals. It also revealed that simply providing information could help lessen them.

Management following whiplash injury can make use of the recommendations as published in the literature. Healthcare professionals must reassure and educate their patients that post-traumatic pain is normal, and that they need to remain active and maintain physical activity in order to improve their prognosis.

Only very few studies have evaluated the adherence of physicians or healthcare professionals to the guidelines and to ways of changing their approach to treatment.

The main aim of this study was to determine what fears and beliefs physicians have about the consequences of whiplash. The secondary aim was to measure the impact of a validated information booklet on emergency physicians' approach to management following a whiplash injury.

Read the detailed description

Once each of the department heads and the different physicians concerned had given their agreement to take part in the study, an initial questionnaire folder (containing the WBQ and FABQ) was sent by email and by post to each of the physicians drawn by randomization. Upon inclusion, demographic data was collected from the physicians (gender, age, place of practice, and length of time in practice), as well as any personal or family history of neck pain or whiplash. The physicians were also asked how often they encountered cases of whiplash.

Information about knowledge of whiplash injury was also sought. This included continuing medical training or recent reading (within the previous 3 years), and in particular knowledge of the different severity grades established by the Quebec Task Force classification, the radiologic recommendations of the Canadian C-Spine Rule, and lastly the latest HAS recommendation on physical therapy in post-whiplash neck pain.

Once the first questionnaire folder had been completed, a second folder was then sent to all physicians participating in the study. The intervention group was instructed to complete the questionnaires at least 48 hours after the intervention that is, after reading the information booklet.

The same items were included as in the initial folder, with an additional questionnaire enabling the intervention group to qualitatively assess the information booklet. If there was no response, reminders were sent by email, then by telephone, and lastly by post.

02

Conditions studied

  • Whiplash Trauma

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Keywords

  • Emergency physician
  • Whiplash Book
  • Whiplash trauma
  • Fears
  • Beliefs
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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 95 is close to the median of 98 across 16 observational studies indexed under Whiplash Injuries.

Browse Whiplash Injuries studies →

Lead sponsor

University Hospital, Clermont-Ferrand is the lead sponsor of 841 studies on the registry; 178 are open to participants now.

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

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Who can participate

Ages eligible
25 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

emergency physicians

Inclusion criteria

    • Both sexes
  • Emergency medicine doctors
  • Doctors has given its consent to participate in the study

Exclusion criteria

Exclusion Criteria:

  • no criteria
05

Study design

Observational model
Other
Time perspective
Other
Enrollment
95 participants (actual)
Patient registry
No

Groups and cohorts

  • intervention group

    The intervention group was instructed to complete the questionnaires at least 48 hours after the intervention that is, after reading the information booklet

    Behavioral: Whiplash book

  • control group

    The same items were included as in the initial folder, with an additional questionnaire enabling the intervention group to qualitatively assess the information booklet. If there was no response, reminders were sent by email, then by telephone, and lastly by post.

    Behavioral: Whiplash book

Interventions

  • BehavioralWhiplash book
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What researchers measure

Primary outcomes

  1. assessment of fears and beliefs in the sample of physicians tested using questionnaire WBQ (whiplash belief questionnaire)

    For each statement, the physician must express his or her level of agreement or disagreement, with a score that varies from 9 to 45. The higher the score, the stronger the beliefs

    Time frame: 48 hours after reading the information booklet

  2. assessment of fears and beliefs in the sample of physicians tested using the FABQ (Fear Avoidance Belief questionnaire)

    The FABQ (Fear Avoidance Belief questionnaire) comprises two independent scales: the physical activity FABQ and work FABQ

    Time frame: 48 hours after reading the information booklet

Secondary outcomes

  1. Measurement of the impact of a validated information booklet on emergency physicians' approach to management following a whiplash injury.

    Time frame: 10 days for control group or minimum 48 hours after reading the information booklet for interventional group

  2. Non-pharmacological management of a whiplash injury

    Non-pharmacological management of a whiplash injury estimated by : * Prescription of necklace (yes/no (%)) If yes, duration of prescription * Prescription of physiotherapy sessions (%) * Work cessation yes/no (%)

    Time frame: 10 days for control group or minimum 48 hours after reading the information booklet for interventional group

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Study locations

1 site
  • CHU Clermont-Ferrand
    Clermont-Ferrand, 63003, France
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 2, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03040245
Lead sponsor
University Hospital, Clermont-Ferrand
Collaborators
CH Aurillac, Jacques Lacarin Hospital Center, CH Moulins, CH Montluçon, CH Issoire, CH Thiers, CH Ambert
Responsible party
Sponsor
First posted
Feb 2, 2017
Start date
Jun 2015
Primary completion
Nov 2016
Completion
Dec 2016
Last update
Feb 2, 2017

Study contacts

Emmanuel COUDEYRE
principal investigator · University Hospital, Clermont-Ferrand
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2017. You cannot join it, but the record below documents what was studied.

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