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Effectiveness of behavioural graded activity compared with physiotherapy treatment in chronic neck pain: a randomised clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN88733332
Enrollment
160
Registered
2004-09-15
Start date
2004-01-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Chronic non-specific neck pain Musculoskeletal Diseases Neck pain

Interventions

The behavioural graded activity program is based on an operant approach, which uses a time-contingent method to increase the patient's activity level. This program is compared with a physiotherapy tre

Sponsors

Erasmus Medical Centre (Netherlands)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 70 years old 2. Have suffered from neck pain for over three months 3. Have an adequate knowledge of the Dutch language Excluded are patients diagnosed with a specific disorder (e.g. a slipped disc, a tumour or a lesion in the cervical spine), those who have had physical/manual therapy during the previous six months, those with a chronic disease (e.g. rheumatoid arthritis or coronary artery disease), or those who have to undergo surgery in the near future.

Exclusion criteria

Exclusion criteria: 1. Diagnosed with a specific disorder (e.g. a slipped disc, a tumour or a lesion in the cervical spine) 2. Have had physical/manual therapy during the previous six months 3. With a chronic disease (e.g. rheumatoid arthritis or coronary artery disease) 4. Who have to undergo surgery in the near future

Design outcomes

Primary

MeasureTime frame
'Global perceived effect' (neck complaint and functioning in daily activities) (1 - 7 on the Likert scale), measured at 4, 9, 26 and 52 weeks.

Secondary

MeasureTime frame
1. Main complaint (0 ? 10 on the Likert scale), measured at baseline, 4, 9, 26 and 52 weeks 2. Pain (Visual Analogue Scale [VAS]), measured at baseline, 4, 9, 26 and 52 weeks 3. Medical consumption (dose per day), measured at baseline, 4, 9, 26 and 52 weeks 4. Coping with Multi-dimensional pain (Multidimensional Pain inventory [MPI] Part I-II and 0 ? 6 on the Likert scale), measured at baseline, 9, 26 and 52 weeks 5. Activity (MPI, part III) (0 ? 6 on the Likert scale), measured at baseline, 4, 9, 26 and 52 weeks 6. Specific functional status (Neck Disability Index [NDI]), measured at baseline, 4, 9, 26 and 52 weeks 7. Quality of life, measured using the 36-item Short Form (SF-36) at baseline, 9, 26 and 52 weeks, and the Euroquol 5-Dutch language version (EQ-5d) at baseline, 4, 9, 26 and 52 weeks 8. Work activities Hours/week, measured at baseline, 9, 26 and 52 weeks 9. Satisfaction about treatment (1 ? 5 on the Likert scale), measured at 4, 9 and 26 weeks 10. Compliance with treatment exercise (number and time per week), measured at 4, 9, 26 and 52 weeks 11. Additional treatments Discipline and number of treatments, measured at 4, 9, 26 and 52 weeks 12. Side-effects (yes ? no and any additional elucidation), measured at 4, 9, 26 and 52 weeks

Countries

Netherlands

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 4, 2026