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Acute whiplash injury study

Acute Whiplash Injury Study (AWIS): a cluster randomised pilot and feasibility trial of an active behavioural physiotherapy intervention for acute Whiplash Associated Disorder (WAD) II management in an insurance private setting

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN84528320
Enrollment
60
Registered
2015-06-18
Start date
2015-11-06
Completion date
Unknown
Last updated
2023-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Whiplash associated disorder (WAD) Musculoskeletal Diseases

Interventions

1. Standard physiotherapy intervention: Each participant will attend a physiotherapy session lasting for 30 minutes once a week. Patients with acute whiplash associated disorder II (WADII) will be man

Sponsors

School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Participants: 1. aged from 18 to 70 years old 2. presenting with WAD grade II from a road traffic accident within the previous four weeks

Exclusion criteria

Exclusion criteria: 1. Signs and symptoms of upper cervical instability or cervical artery dysfunction 2. Suspected serious spinal pathology 3. Open wounds 4. Active inflammatory arthritis 5. Tumours 6. Infection of the skin and soft tissue 7. Bleeding disorders or using anti-coagulant medication 8. Any current or previous treatment from any other third party or presenting with any serious injuries from other areas of the body resulting from the accident 9. History of cervical surgery,previously symptomatic degenerative diseases of cervical spine within 6 months before road traffic accident 10. Previous history of whiplash or other neck pain 11. Alcohol abuse 12. Dementia 13. Serious mental diseases 14. Psychiatric diseases 15. Non-native English speaking

Design outcomes

Primary

MeasureTime frame
Neck Disability Index (NDI)

Secondary

MeasureTime frame
1. Visual Analogue Scale (VAS) for pain intensity 2. Cervical Range of Motion (CROM) 3. Pressure Pain Threshold (PPT) 4. Impact of Events Scale (IES) 5. Fear Avoidance Beliefs Questionnaire (FABQ) 6. Quality of Life (EQ5D-5L)

Countries

England, United Kingdom

Contacts

Public ContactTaweewat Wiangkham

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 1, 2026