Retention in physically demanding jobs of individuals with low back pain: study protocol for a randomised controlled trial
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Retention in physically demanding jobs of individuals with low back pain : study protocol for a randomised controlled trial. / Brandt Hansen, Bjarke; Kirkeskov, Lilli; Christensen, Robin; Begtrup, Luise Mølenberg; Pedersen, Ellen Bøtker; Teilya, Jakob Falk; Boesen, Mikael; Fournier, Gilles Ludger; Bliddal, Henning; Kryger, Ann Isabel.
I: Trials, Bind 16, 166, 16.04.2015.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Retention in physically demanding jobs of individuals with low back pain
T2 - study protocol for a randomised controlled trial
AU - Brandt Hansen, Bjarke
AU - Kirkeskov, Lilli
AU - Christensen, Robin
AU - Begtrup, Luise Mølenberg
AU - Pedersen, Ellen Bøtker
AU - Teilya, Jakob Falk
AU - Boesen, Mikael
AU - Fournier, Gilles Ludger
AU - Bliddal, Henning
AU - Kryger, Ann Isabel
PY - 2015/4/16
Y1 - 2015/4/16
N2 - BACKGROUND: Low back pain is prevalent and is a frequent cause of disability and sick leave among working adults. Individuals with low back pain often consult general practice or other health care providers which often results in a unilateral intervention focussed on their symptoms. Employment is associated with physical and mental well-being, so, patients may benefit from an early additional occupational medicine intervention. For individuals with physically demanding jobs it can be especially challenging to retain their jobs. The aim of the 'GoBack trial' is to develop and evaluate the efficacy and feasibility of an occupational medicine intervention for individuals with low back pain in physically demanding jobs.METHODS/DESIGN: We will conduct a randomised controlled trial enrolling 300 participants with difficulty in maintaining physically demanding jobs due to low back pain for a current period of 2 to 4 weeks. Participants will be randomised and stratified according to their age and gender before being allocated in a 1:1 ratio to either control or additional occupational medicine intervention. Both groups will receive conventional treatment for their low back pain during the study. All participants will be thoroughly assessed for causes of low back pain and potential prognostic factors by questionnaires, clinical specialist assessments and magnetic resonance imaging (MRI) scans of the lumbar spine. Primary outcome is the accumulated duration of self-assessed sick leave (in days) due to low back pain during 6 months from baseline. Secondary outcomes include general self-rated back pain, disability and screening for potential prognostic factors: fear avoidance behaviour, disability, health status and degenerative MRI findings. For tertiary purposes selected outcomes will also be assessed after 1 and 2 years from baseline.DISCUSSION: Many guidelines exist for the management of low back pain, but they provide limited guidance on occupational aspects. The findings from this randomised trial will provide high-quality evidence for the efficacy and feasibility of an occupational medicine intervention model for individuals with low back pain in physically demanding jobs.TRIAL REGISTRATION: This trial was registered with ClinicalTrials.gov (identifier: NCT02015572 ) on 29 November 2013.
AB - BACKGROUND: Low back pain is prevalent and is a frequent cause of disability and sick leave among working adults. Individuals with low back pain often consult general practice or other health care providers which often results in a unilateral intervention focussed on their symptoms. Employment is associated with physical and mental well-being, so, patients may benefit from an early additional occupational medicine intervention. For individuals with physically demanding jobs it can be especially challenging to retain their jobs. The aim of the 'GoBack trial' is to develop and evaluate the efficacy and feasibility of an occupational medicine intervention for individuals with low back pain in physically demanding jobs.METHODS/DESIGN: We will conduct a randomised controlled trial enrolling 300 participants with difficulty in maintaining physically demanding jobs due to low back pain for a current period of 2 to 4 weeks. Participants will be randomised and stratified according to their age and gender before being allocated in a 1:1 ratio to either control or additional occupational medicine intervention. Both groups will receive conventional treatment for their low back pain during the study. All participants will be thoroughly assessed for causes of low back pain and potential prognostic factors by questionnaires, clinical specialist assessments and magnetic resonance imaging (MRI) scans of the lumbar spine. Primary outcome is the accumulated duration of self-assessed sick leave (in days) due to low back pain during 6 months from baseline. Secondary outcomes include general self-rated back pain, disability and screening for potential prognostic factors: fear avoidance behaviour, disability, health status and degenerative MRI findings. For tertiary purposes selected outcomes will also be assessed after 1 and 2 years from baseline.DISCUSSION: Many guidelines exist for the management of low back pain, but they provide limited guidance on occupational aspects. The findings from this randomised trial will provide high-quality evidence for the efficacy and feasibility of an occupational medicine intervention model for individuals with low back pain in physically demanding jobs.TRIAL REGISTRATION: This trial was registered with ClinicalTrials.gov (identifier: NCT02015572 ) on 29 November 2013.
KW - Absenteeism
KW - Adolescent
KW - Adult
KW - Aged
KW - Clinical Protocols
KW - Denmark
KW - Feasibility Studies
KW - Female
KW - Humans
KW - Job Description
KW - Low Back Pain
KW - Magnetic Resonance Imaging
KW - Male
KW - Middle Aged
KW - Occupational Health
KW - Pain Management
KW - Pain Measurement
KW - Patient Care Team
KW - Personnel Turnover
KW - Research Design
KW - Return to Work
KW - Sick Leave
KW - Surveys and Questionnaires
KW - Time Factors
KW - Treatment Outcome
KW - Work Capacity Evaluation
KW - Workload
KW - Young Adult
U2 - 10.1186/s13063-015-0684-3
DO - 10.1186/s13063-015-0684-3
M3 - Journal article
C2 - 25887302
VL - 16
JO - Trials
JF - Trials
SN - 1745-6215
M1 - 166
ER -
ID: 159080895