Skip to content

Supervised Walking In comparison to Fitness Training for back pain

A single-blinded randomised controlled trial exploring the effectiveness of a walking programme and a supervised general exercise programme versus usual physiotherapy for chronic low back pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17592092
Enrollment
246
Registered
2009-01-08
Start date
2008-10-01
Completion date
Unknown
Last updated
2019-09-09

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

Conditions

Chronic low back pain Musculoskeletal Diseases Dorsalgia

Interventions

1. Walking programme (WP): Within two weeks of randomisation participants will commence participation in the WP at each participating hospital through an appointment with a Chartered P
recording of the patient's exercise capabilities and perceived barriers to recovery and the individual's treatment expectations. Each subject will be given a pedometer to wear for seven days to record
the minimum being a 10-minute walk (approx 1200 steps) on at least four days per week to be decided with, where possible, one day's rest between walks. The aim of the programme is to progress to the A

Sponsors

Health Research Board (HRB) (Ireland)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with chronic (greater than or equal to three months) or recurrent (greater than or equal to three episodes in previous 12 months) LBP of mechanical origin with/without radiation to the lower limb 2. Males/females between 18 - 65 years 3. No spinal surgery within the previous 12 months 4. Patients deemed suitable by their General Practitioner (GP)/hospital consultant to carry out an exercise programme 5. Patients willing to attend for an 8-week treatment programme of exercise classes 6. Access to a telephone (for follow-up support) 7. Fluency in English (verbal and written) 8. Low levels of physical activity measured by the International Physical Activity Questionnaire (IPAQ) (less than 600 MET-minutes/week)

Exclusion criteria

Exclusion criteria: 1. Currently or having received treatment for chronic low back pain (CLBP) within previous three months 2. Red flags indicating serious spinal pathology, e.g. cancer, cauda equina lesion 3. Radicular pain indicative of nerve root compression 4. Patients diagnosed with severe spinal stenosis, spondylolisthesis, fibromyalgia 5. History of systemic/inflammatory disease, e.g. rheumatoid arthritis 6. Patients with any confounding conditions such as a neurological disorder or currently receiving treatment for cancer 7. Patients with acute (less than six weeks) or subacute LBP (6 - 12 weeks), provided that they have experienced less than three LBP episodes during previous 12 months 8. Unstable angina/uncontrolled cardiac dysrhythmias/severe aortic stenosis/acute systemic infection accompanied by fever 9. Medico-legal issues

Design outcomes

Primary

MeasureTime frame
Oswestry Disability Index, measured at 3, 6 and 12 months by postal follow-up.

Secondary

MeasureTime frame
1. Pain using a Numerical Rating Scale 2. Health-related quality of life measured by the EuroQol questionnaire 3. Psychosocial beliefs using the Fear Avoidance Beliefs Questionnaire and the Back Beliefs Questionnaire 4. Number of days reported sick leave over the past year for those in paid employment only 5. Physical activity levels using the International Physical Activity Questionnaire (IPAQ), an exercise diary and the activPalTM accelerometer 6. Patient satisfaction will be assessed using Likert scales assessing satisfaction with outcome and satisfaction with care 7. Self efficacy questionnaire The outcomes will be measured at 3, 6 and 12 months by postal follow-up.

Countries

Ireland

Outcome results

None listed

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