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The UK Back pain, Exercise Active management and Manipulation trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN32683578
Enrollment
1350
Registered
2000-10-23
Start date
1997-09-01
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

Primary care Musculoskeletal Diseases Dorsalgia

Interventions

General practices randomised between: I. An active management training programme and conventional management Patients within practices randomised between: II. A spinal manipulation package agreed rec

Sponsors

Medical Research Council (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Primary care back pain consultors aged between 18 and 65 years 2. Non-specific back pain 3. Referred leg pain must be predominantly above knee 4. Fluent in English - able to read and write 5. No physical therapies in previous 3 months 6. Duration at least 4 weeks 7. Roland Disability Questionnaire (RDQ) score of 4 or more

Exclusion criteria

Exclusion criteria: 1. People over 65 2. Clinical indications for the investigation of possible serious spinal or neurological pathology, or for urgent surgical referral 3. Nerve root pain 4. Previous spinal surgery 5. Major psychological complication or abnormal illness behaviour, referred to a tertiary pain management programme 6. Other musculoskeletal disorders which would interfere with therapy 7. History of psychosis or major alcohol abuse 8. Other concurrent medical conditions, including cardiovascular disease 9. Moderate to severe hypertension 10. Long-term steroid use 11. Anti-coagulant therapy 12. Perceived inability to walk 100 metres when free of pain 13. Unable to get up and down off floor unaided 14. Physical therapy (including acupuncture) in the previous 3 months 15. Unable to read and write fluently in English 16. Roland Disability questionnaire score of 3 or less on the day of randomisation

Design outcomes

Primary

MeasureTime frame
The primary outcome measure is the change in Roland Disability Questionnaire (RDQ) score at 3 and 12 months. A change of 2.5 points on the scale has been agreed by the UK BEAM Working Party and Trial Steering Committee as clinically significant.

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 2, 2026