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Function After Spinal Treatment, Exercise and Rehabilitation: Improving the functional outcome of spinal surgery

Function After Spinal Treatment, Exercise and Rehabilitation: Improving the functional outcome of spinal surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN46782945
Enrollment
344
Registered
2005-01-21
Start date
2005-04-01
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Spinal lateral root stenosis and discectomy Surgery Spinal surgery

Interventions

Current interventions as of 26/06/2008: Rehabilitation Programme: Patients randomised to the rehabilitation arms of the study will commence the programme 6 to 8 weeks following surgery. The programm

Sponsors

Arthritis Research Campaign (ARC) (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Current inclusion criteria as of 26/06/2008: Eligible patients at participating hospitals are those currently on the waiting list for spinal surgery with either: 1. Signs, symptoms and radiological evidence of lateral nerve root compression, that is, patients presenting with radicular pain with an associated neurological deficit or with neurogenic claudication (pain in the buttock, thigh or leg that improves with rest), or 2. Lumbar disc prolapse, that is, patients with root symptoms and signs and magnetic resonance imaging (MRI) confirmation of lumbar disc herniation Previous inclusion criteria: People with low back and leg pain

Exclusion criteria

Exclusion criteria: Added as of 26/06/2008: 1. Any condition where either the intervention or the rehabilitation may have an adverse effect on the individual 2. Previous spinal surgery 3. Spinal surgery where a fusion procedure is planned due to the unknown hazards of the activity programme for this type of surgery 4. Pregnant women 5. Inadequate ability to complete the trial assessment forms 6. Any patient who is unable to attend the rehabilitation or the reviews or who is unsuitable for rehabilitation classes 7. Unable to complete outcome measures

Design outcomes

Primary

MeasureTime frame
Added as of 26/06/2008: Oswestry Disability Index

Secondary

MeasureTime frame
Added as of 26/06/2008: 1. An economic analysis based on costs and EQ-5D (a validated, global measure of quality of life) 2. Visual analogue scales of back and leg pain 3. Measures of patient expectations and satisfaction 4. Return to work 5. Frequency of re-operation 6. Hospital Anxiety and Depression Scale (HADS) 7. Physical activity scale of the Fear Avoidance Beliefs Questionnaire

Countries

United Kingdom

Outcome results

None listed

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