Relationship between self-reported disability, performance based disability and psychological factors in patients with complaints of whiplash.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON23925

Enrollment

Registered

2010-09-15

Start date

2010-10-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

whiplash, disability, functional capacity evaluation, psychological

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. A WAD I-II diagnosis by a doctor; 2. Complaints six months or longer; 3. Age between 18 and 65 years; 4. Patients are with sick leave.

Exclusion criteria

Exclusion criteria: 1. Co-morbidity with severe negative consequences for functioning; 2. A diagnosis of psychiatric illness; 3. Insufficient knowledge of the Dutch language; 4. Severe neck problems before the trauma like arthrosis or hernias.

Design outcomes

Primary

Measure	Time frame
1. The “Neck Disability Index” (self-reported disability); 2. The Neck specific version of the Functional Capacity Evaluation for neck complaints (performance based disability).	—

Secondary

Measure	Time frame
1. The triaxial accelerometer to measure the actual performance; 2. The TAMPA to measure fear of movement; 3. The 4DSQ to measure depression, anxiety and distress; 4. The UCL to measure coping styles; 5. The CIS20R to measure fatigue; 6. The Pain Self Efficacy Questionnaire to measure self efficacy; 7. The RAND to measure quality of life; 8. The VAS to measure the level of pain; 9. The demographic information consist of gender, age, height, weight, marital status, duration of complaints, present medication, education level, working status and claim status.	—

Measure

Time frame

1. The triaxial accelerometer to measure the actual performance; 2. The TAMPA to measure fear of movement; 3. The 4DSQ to measure depression, anxiety and distress; 4. The UCL to measure coping styles; 5. The CIS20R to measure fatigue; 6. The Pain Self Efficacy Questionnaire to measure self efficacy; 7. The RAND to measure quality of life; 8. The VAS to measure the level of pain; 9. The demographic information consist of gender, age, height, weight, marital status, duration of complaints, present medication, education level, working status and claim status.

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Contacts

Public ContactS. Meer, van der

Colosseum 40

svandermeer@condite.nl+31 (0)53 4281144

Outcome results