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The effectiveness of motorised lumbar traction in the management of lumbosacral nerve root pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN78417198
Enrollment
30
Registered
2007-03-21
Start date
2004-03-01
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

Low back pain Musculoskeletal Diseases Back pain

Interventions

Group 1: Manual therapy, exercise and advice Group 2: Manual therapy, exercise, advice and continous lumbar traction

Sponsors

University of Ulster (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 65 years of age (male and female), presenting with acute/sub-acute LBP with accompanying radiculopathy 2. ?Nerve root? was identified by the presence of: a. dermatomal pain distribution radiating below the knee (one or both limbs) b. sharp/severe quality, often worse in the leg than back (leg pain threshold of 3/10 on Visual Analogue Scale [VAS]) With at least one of the following signs and symptoms: c. pins and needles in the distal dermatome (where this was present patients with leg pain were accepted even if not extending below the knee) d. increased pain in the leg on coughing, sneezing or straining e. neurological deficit, i.e., decreased muscle strength/sensory loss/reflex loss f. positive straight leg raise test stretch, i.e., limb pain reproduced on test 3. Acute/sub acute LBP, defined as LBP of less than 12 weeks duration, or a recurrent episode with a pain free period of at least three months prior to the onset of this episode. Only one study has considered recovery rates with ?sciatica? and reported that both back and leg pain decreased, on average, by 69%, and disability decreased by 57% within one month from onset. Current physiotherapy practice would suggest that treatment begins as soon as possible; therefore patients were accepted after four weeks of onset of leg pain 4. Able to attend for physiotherapy two to three times a week for four to six weeks 5. Patients were literate with English as their first language

Exclusion criteria

Exclusion criteria: 1. Previous spinal surgery 2. Formal therapeutic or medical intervention within the last three months (e.g., epidural injection, facet joint block, physiotherapy etc..,) 3. Co-existing conditions (anklyosing spondolytitis, rheumatoid arthritis, spinal stenosis [diagnosed], spondolythesis, recent spinal fracture, spinal tumor or a patient where secondary metastases was suspected) 4. Concomitant severe medical problem preventing participation in the trial (cardiac condition, respiratory conditions, neurological disorder or organ disease) 5. Long term oral steroid intake (due to the risk of osteoporosis) 6. Current anti-coagulant therapy or blood clotting disorders 7. Pregnancy 8. History of major psychiatric illness 9. Roland Morris disability questionnaire score of below four, and/or a VAS score of less than three on a ten point scale for leg pain (to avoid floor effects)

Design outcomes

Primary

MeasureTime frame
1. Roland Morris Disability Questionnaire 2. McGill pain questionnaire 3. Acute low back pain screening questionnaire 4. Short Form health survey 36

Secondary

MeasureTime frame
1. Visual analogue scale - pain 2. Medication diary 3. Percentage improved - subjective patient score

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 6, 2026