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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00206271
Other study ID # 20000268
Secondary ID
Status Completed
Phase Phase 3
First received September 13, 2005
Last updated September 13, 2005
Start date May 2001
Est. completion date October 2004

Study information

Verified date September 2005
Source The Back Research Center, Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

Background: Long-lasting pain and disability, known as chronic whiplash-associated disorder (WAD), may develop after forced flexion-extension trauma to the cervical spine. Mechanisms behind WAD are virtually unknown, as are the possible effects of early intervention. This trial was undertaken to compare the effect of three early intervention strategies for the prevention of developing chronic WAD following acute whiplash injury.

Methods: 458 participants were randomised to one of 1) stiff neck collar, 2) advice to act-as-usual, or 3) an active mobilisation regime. Participants were followed for one year and treatment effects were compared in terms of lasting neck pain, headache, disability and sick-leave.


Recruitment information / eligibility

Status Completed
Enrollment 450
Est. completion date October 2004
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Been exposed to rear-end or frontal car collision

- Experienced symptoms within 72 hours

- 18 – 70 years

Exclusion Criteria:

- Could not be enrolled within 10 days of the collision

- Fractures or dislocations of the cervical spine

- Amnesia for the accident

- Unconsciousness in relation to the accident

- Injuries other than the whiplash injury

- Average neck pain during the preceding 6 months exceeding 2 on a box scale 0-10, where 0= no pain and 10= worst possible pain

- Significant pre-existing somatic or psychiatric disease

- Alcohol or drug abuse

- Does not read or understand Danish.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
neck collar; advice to act-as-usual; active mobilisation


Locations

Country Name City State
Denmark The Back Research Center 5750 Ringe
Denmark Danish Pain Research Center 8000 Aarhus

Sponsors (2)

Lead Sponsor Collaborator
The Back Research Center, Denmark Danish Pain Research Center

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Neck pain intensity
Primary Headache intensity
Primary Neck disability
Primary Sick leave during the 12 month after inclusion
Secondary Medication
Secondary Number of non-painful complaints
Secondary General health
See also
  Status Clinical Trial Phase
Recruiting NCT01360138 - A Clinical Comparison in Cervical Epidural Pressure Changes Between Midline and Paramedian Approaches N/A
Completed NCT03784196 - Changes of Pain Sensitivity During Rehabilitation of Patients Suffering From Whiplash Associated Disorders
Recruiting NCT01824810 - Whiplash-associated Disorders - Needling Treatments Pilot Study N/A
Enrolling by invitation NCT01544075 - Efficacy of Pain Neurophysiology Education in Combination With Psychologic Inoculation in Chronic Whiplash Phase 0