Low Back Pain
Conditions
Brief summary
This study aims to investigate if a low back pain screening tool is helpful for the caregivers to direct the rehabilitation in a more efficient way, at an earlier stage. Primary Health care centers in the municipality of Halmstad, Sweden will be enrolled to participate in the study as either Control or intervention. The primary Health care centers who are enrolled taking part in the intervention, will use the provided screening tool when taking care of patients seeking care for low back pain. Scorings from the screening tool will label the patients as one of Three pre-defined risk levels. The caregiver will then use the provided risk level when deciding how to proceed the rehabilitation. Based on the risk level identified, the patient is directed to one of three levels of treatments - including simple advice; physiotherapy; or multimodal rehabilitation. The screening tool is used as a complement to the examination, allowing the physiotherapist /GP to decide how to proceed with rehabilitation using the back screening tool, together with Clinical examinations. The Control Group consists of patients recruited when seeking care for back pain at a Primary Health Care service who has been randomly selected as Control. The care givers at the Control primary Health care will conduct as usual, not using the back pain screening tool in their Clinical examinations.
Interventions
OTHERBack pain screening test
The care giver use the screening tool in order to score the back patient to three levels of risk. For each level of risk, one suggested type of care is provided; 1) simple advise; 2) physiotherapy; 3) multimodal rehabilitation. highest risk level includes multimodal intervention.
Sponsors
FoU Center Spenshult
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to 67 Years
Healthy volunteers
No
Inclusion criteria
* Seeking care for low back pain at any of the included primary Health care.
Exclusion criteria
* Red flags
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of physiotherapy treatments | 4 months after inclusion | Number of treatments given by physiotherapist |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| back pain questionnaire - The Keele STarT Back Screening Tool | 4 months after inclusion | The Keele STarT Back Screening Tool, is a prognostic tool helping clinicians identify risk factors for persistent back pain. 9 questions. Total score range from 0 to 9 (best- to worse) |
| back pain questionnaire - Pain distribution | 4 months after inclusion | Pain distribution (numbers of marked regions and location) will be measured by a pain mannequin divided into 18 body regions.The patients mark each region with pain lasting more than three months during the past 12 months. The total number of regions giving a total score 0-18 (few to several regions, best- to worse). |
| back pain questionnaire - The Roland-Morris Disability Questionnaire | 4 months after inclusion | The Roland-Morris Disability Questionnaire assess self-rated physical disability Total score range from 0-24 (best to worse disability) |
| work ability - Work productivity and activity impairment questionnaire (WPAI) | 4 months after inclusion | Work productivity and activity impairment questionnaire (WPAI) with 6 questions assessing the impact of the disease on work and other daily activities during the previous 7 days (absenteeism, presenteeism, impaired activities outside work, and overall work impairment). Each component is expressed as percentage of impairment due to the disease (0-100%) where a higher percentage indicates a greater reduction. |
| work ability - The work ability index (WAI) | 4 months after inclusion | The work ability index (WAI) single-item question concerned the item current work ability compared with the lifetime best, with a possible score of 0 (completely unable to work) to 10 (work ability at its best) |
Countries
Sweden
Contacts
Primary ContactEmma Haglund, PhD
Backup ContactMaria Andersson, PhD
Outcome results
None listed