Skip to content

Cognitive Muscular Therapy - developing a training programme for physiotherapists

Behaviour change to rEduce LOW back pain: a training development study (BELOW)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN31860277
Enrollment
15
Registered
2024-06-21
Start date
2024-07-01
Completion date
Unknown
Last updated
2026-06-15

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

Interventions

Patient participant flow through the study: 1. Participant receives the participant information sheet through the post. 2. Participant gets in touch and discusses the study with the research coordinat

Sponsors

University of Salford
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Adults presenting with low back pain (LBP) pain duration >3 months and considered at high risk of poor long-term outcome (identified with STarTBack 9item tool) 2. Currently scoring 4 or more on a numerical response scale for pain from 0-10 (0 = no pain, 10 = worst pain) 3. Ability to stand for 10 minutes and walk for 5 minutes (required to complete the intervention) 4. Speak and understand English sufficiently to read the information sheet and sign the consent form

Exclusion criteria

Exclusion criteria: 1. Diagnosis of inflammatory arthritis 2. LBP due to pregnancy and up to 12 months post pregnancy 3. Previous spinal surgery such as discectomy, anterior cervical discectomy and fusion, disc replacement, laminectomy and scoliosis fixation 4. Diagnosis of degenerative neurological disorders (e.g. multiple sclerosis/Parkinson’s disease) 5. BMI of more than 33 (as increased subcutaneous fat prevents the collection of surface EMG signals) 6. Pending litigation related to an injury, for example, at work or whilst driving 7. Vulnerable patients, for example, those who lack the mental capacity to make decisions, have dementia or are nearing the end of life

Design outcomes

Primary

MeasureTime frame
1. Pain measured using the Numerical Rating of Pain Scale at baseline and 10 weeks 2. Disability measured using the Roland Morris Disability Questionnaire at baseline and 10 weeks 3. Catastrophising measured using the Pain Catastrophising Scale (PCS) at baseline and 10 weeks 4. Risk of chronic pain measured using the STarT Back Screening Tool at baseline and 10 weeks

Secondary

MeasureTime frame
There are no secondary outcome measures

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Jun 21, 2026