- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01882686
Efficacy of a Classification Based 'Cognitive Functional Therapy' in Nurses With Non Specific Chronic Low Back Pain
Efficacy of a Classification Based 'Cognitive Functional Therapy' in Nurses With Non Specific Chronic Low Back Pain - a Series of Case-controls
A series of case-studies to explore the efficacy of classification based cognitive functional physiotherapy according to the classification system proposed by Peter O'Sullivan in specific nursing population with non specific chronic low back pain.
The investigators hypothesis was that treatment targeting the mechanisms behind the problem from a multidimensional perspective would be effective to reduce pain, disability and sick-leave.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Low back pain (LBP) is a common, recalcitrant and costly health problem, which limits patients' daily activities. In 85% of the cases, LBP is classified as 'non-specific', which means there is no clear underlying patho-anatomical/radiological abnormality. This subgroup often gives rise to a chronic fluctuating problem. Although most cases of LBP resolve within 8 to 12 weeks, it may become chronic in up to 15% of patients. LBP constitutes an enormous and growing medical and socio-economical problem for the modern society. Nursing has been identified amongst the top professions at risk for occupational LBP, with lifetime prevalence between 66%-82%. The impact of LBP for nurses includes time off work, increased risk of chronicity, associated personal and economic costs and reduced nursing workforce efficiency.
Non Specific Chronic Low Back Pain (NSCLBP) is widely viewed as a multifactorial biopsychosocial pain syndrome. It has been proposed by several authors that NSCLBP represents a vicious cycle associated with different combinations of maladaptive; cognitive (negative beliefs, fear avoidance behaviours, catastrophising, depression, stress, lack of pacing and coping), physical (pain provocative postures, movement patterns and pain behaviours) and lifestyle (inactivity, rest) behaviours that act to promote pain and disability. However a recent systematic review suggests that this change in paradigm and the investigators new understanding of NSCLBP has not resulted in clinical trials utilizing multidimensional classification systems or targeted interventions based on the underlying mechanisms. In line with this paradigm shift a novel multidimensional classification system has been developed incorporating the biopsychosocial model, which subgroups patients based on their underlying pain mechanism. Enabling a classification based interventions targetting the maladaptive cognitive, physical and lifestyle behaviours associated with the disorder.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Antwerpen
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Lille, Antwerpen, Belgium, 2275
- Lindelo
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Low Back Pain (LBP) with/without referred pain in buttock/thigh for > 3 months, including the four weeks prior to testing
- LBP is primarily localised from T12 to gluteal folds
- mechanical provocation of LBP with postures, movement and activities
- average pain intensity in the past week Numerical Rating Scale (NRS) >/= 1/10
- Disability (ODI) >/=2%
- willingness to sign the informed consent
Exclusion Criteria:
- specific spinal pathology
- presence of red flags
- previous lumbar spinal surgery
- pregnancy
- diagnosed psychiatric disorder - somatisation
- radicular pain with positive neural tissue provocation test
- widespread non-specific pain disorder (no primary LBP focus)
- specific diagnoses: active rheumatologic disease, progressive neurological disease, serious cardiac or other internal medical condition, malignant basic diseases, acute traumas, infections, or acute vascular catastrophes
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Classification Based Cognitive Functional Therapy
|
A novel multidimensional classification system has been developed incorporating the biopsychosocial model, which subgroups patients based on their presentation.
This subclassification is the base for matched interventions directed at the maladaptive cognitive, physical and lifestyle behaviours associated with the disorder.
The intervention is called 'cognitive functional therapy' as it directly challenges these behaviours in a functionally specific and graduated manner.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in pain
Time Frame: 3, 6, 9 and 12 months
|
Pain was assessed using a numerical pain rating scale (NPRS) ranging from 0 (no pain) to 10 (worst imaginable pain)
|
3, 6, 9 and 12 months
|
|
Change from baseline in disability
Time Frame: 3, 6, 9 months, 1 and 3 year
|
Disability was measured using the Oswestry Disability Index (ODI)
|
3, 6, 9 months, 1 and 3 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in Beliefs about LBP
Time Frame: 3, 6, 9 and 12 months
|
Back Beliefs Questionnaire (BBQ)
|
3, 6, 9 and 12 months
|
|
Change from baseline in Chance of long-term disability and failure to return to work
Time Frame: 3, 6, 9 and 12 months
|
Tha Acute Low Back Pain Screening Questionnaire (Dutch version of the Ørebro Pain Screening Questionnaire) is a 'yellow flag' screening tool that predicts long-term disability and failure to return to work due to personal and environmental factors.
|
3, 6, 9 and 12 months
|
|
Change from baseline in Physical activity
Time Frame: 3, 6, 9 and 12 months
|
Baecke questionnaire
|
3, 6, 9 and 12 months
|
|
Change from baseline in Sleep problems
Time Frame: 3, 6, 9 and 12 months
|
Insomnia Severity Index (ISI)
|
3, 6, 9 and 12 months
|
|
Change from baseline in Depression, anxiety and stress
Time Frame: 3, 6, 9 and 12 months
|
Depression Anxiety and Stress scale (DASS-21)
|
3, 6, 9 and 12 months
|
|
Change from baseline in Self-efficacy, coping
Time Frame: 3, 6, 9 and 12 months
|
Pain Self-Efficacy Questionnaire (PSEQ)
|
3, 6, 9 and 12 months
|
|
Change from baseline in Fear-avoidance / kinesiophobia
Time Frame: 3, 6, 9 and 12 months
|
Tampa Scale of Kinesiophobia (TSK-17)
|
3, 6, 9 and 12 months
|
|
Change from baseline in Pain catastrophizing
Time Frame: 3, 6, 9 and 12 months
|
Pain Catastrophizing Scale (PCS)
|
3, 6, 9 and 12 months
|
|
Change from baseline in Psychosocial job aspects
Time Frame: 3, 6, 9 and 12 months
|
The Job Content Questionnaire (JCQ) is a tool for psychosocial job assessment.
|
3, 6, 9 and 12 months
|
|
Change from baseline in Lower Lumbar spine Kinematics
Time Frame: 3, 6, 9 and 12 months
|
Lower Lumbar kinematics of the spine were measured with the BodyGuard (sels-instruments nv).
This is a remote measuring system.
|
3, 6, 9 and 12 months
|
|
Patient satisfaction of the intervention
Time Frame: 3, 6, 9 and 12 months
|
Patients' Global Impression of Change (PGIC) scale
|
3, 6, 9 and 12 months
|
|
Change from baseline in Category of risk of poor outcome (persistent disabling symptoms)
Time Frame: 3, 6, 9 and 12 months
|
The Start Back Screening Tool is used to screen primary care patients with low back pain for prognostic indicators that are relevant to initial decision making.
The tool helps to group patients into 3 categories of risk of poor outcome (persistent disabling symptoms) - low, medium, and high-risk.
|
3, 6, 9 and 12 months
|
|
Change from baseline in Psychosocial aspects of work
Time Frame: 3, 6, 9 and 12 months
|
Psychosocial Aspects of Work Questionnaire (PAWQ)
|
3, 6, 9 and 12 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Wim Dankaerts, KU Leuven
Publications and helpful links
General Publications
- Vibe Fersum K, O'Sullivan P, Skouen JS, Smith A, Kvale A. Efficacy of classification-based cognitive functional therapy in patients with non-specific chronic low back pain: a randomized controlled trial. Eur J Pain. 2013 Jul;17(6):916-28. doi: 10.1002/j.1532-2149.2012.00252.x. Epub 2012 Dec 4.
- O'Sullivan P. Diagnosis and classification of chronic low back pain disorders: maladaptive movement and motor control impairments as underlying mechanism. Man Ther. 2005 Nov;10(4):242-55. doi: 10.1016/j.math.2005.07.001. Epub 2005 Sep 9.
- Dankaerts W, O'Sullivan P. The validity of O'Sullivan's classification system (CS) for a sub-group of NS-CLBP with motor control impairment (MCI): overview of a series of studies and review of the literature. Man Ther. 2011 Feb;16(1):9-14. doi: 10.1016/j.math.2010.10.006. Epub 2010 Nov 20.
- Van Hoof W, O'Sullivan K, Verschueren S, O'Sullivan P, Dankaerts W. Evaluation of Absenteeism, Pain, and Disability in Nurses With Persistent Low Back Pain Following Cognitive Functional Therapy: A Case Series Pilot Study With 3-Year Follow-Up. Phys Ther. 2021 Jan 4;101(1):pzaa164. doi: 10.1093/ptj/pzaa164.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- S54606
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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