Viewing Study NCT00526604



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Last Modification Date: 2024-10-26 @ 9:36 AM
Study NCT ID: NCT00526604
Status: TERMINATED
Last Update Posted: 2011-07-06
First Post: 2007-09-06

Brief Title: Work Related Rehabilitation in Patients With Low Back Pain
Sponsor: Ullevaal University Hospital
Organization: Oslo University Hospital

Study Overview

Official Title: A Study on the Effect of Employment Follow-up on Return to Work in Sick Listed Patients With Low Back Pain
Status: TERMINATED
Status Verified Date: 2008-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: The study was stopped as the another multicentre-RCT on the same patients started
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Low back pain is a usual conditions in the western countries and several treatments available for patients with non-specific low back pain According to the European guidelines are exercise and cognitive intervention effective on pain and functionwwwbackpaineuropeorg but it have no documented effect on return to work In addition there is no documentation that treatments which focus on a single treatment is effective with regard to return to work for sick-listed patients

The challenges for health personnel is not cure of the patients back pain but to build up rehabilitation programs which focus on disability and work incapacity in patients which are at risk of loosing their work Dr P Loisel Montreal Canada has since 1995 treated patients with back pain according to the The PREVICAP model - PREVention of work handICAP where the main purpose with work-related program is to prevent prolonged disability and to help patients back to work Loisel demonstrated that the PREVICAP models accelerated the return to work factor by a factor 24 p001 The PREVICAP model have also been evaluated in Amsterdam by Dr Anema with the same results

At the Back Clinic Ullevål University Hospital we have evaluated several exercise programs with good effect on pain and function but not on the return to work rate We are planning to do a randomized controlled trial after the PREVICAP model All included patients in both groups will have an clinical examination by specialist in Physical Medicine and Rehabilitation and an exercise program Patients will be randomized to a work-related rehabilitations program or to usual care by the general practitioner

Hypothesis Main hypothesis Sick-listed patients with back pain who will be randomized to the work-related rehabilitation programs will return to work faster than patients randomized to usual care by the general practitioner

Second hypothesis A cost-benefit analysis will favor the exercise program and work place intervention
Detailed Description: Background Low back pain is a usual conditions in the western countries and in Norway 40 of the population report decreased function because of back pain The disease has great economic consequences which in 2004 came to 15 billions to disability pension and 146 billions to physical treatments

Severe incidence of back pain like tumours infections fractures and pareses are rare and represent less than 1 of all cases The main part is within the category of non-specific low back pain which is defined as back pain without specific pathology as known cause

Based on scientific documentation the back-specialists consider non-specific low back pain as a benign and self-limited condition while patients expect to get treatment because they experience the condition as painful and disabling

There are several treatments available for patients with non-specific low back pain According to the European guidelines exercise and cognitive intervention has good effects on pain and function wwwbackpaineuropeorg but it is not documented effect on return to work In addition it is not documented that treatments which focus on a single treatment neither is effective regarding return to work for sick-listed patients

It is a usual myth that physical hard work cause back pain However only few studies have demonstrated correlations between hard work and sick-leave On the contrary several studies have demonstrated that back pain is a multifactorial problem which is not only due to workers characteristics but is also closely related to environmental factors such as the workplace the healthcare system the compensation system and the interaction between all stakeholders in the disability problem

The challenges for health personnel is not cure of the patients back pain but to build up rehabilitation programs which focus on disability and work incapacity in patients which are at risk of loosing their work

Dr P Loisel Montreal Canada has since 1995 treated patients with back pain according to the The PREVICAP model - PREVention of work handICAP The main purpose with work-related program is to prevent prolonged disability and to help patients back to work This approach includes two steps first identification of factors on the workplace which contribute to the absence of work and second workplace intervention Identification of factors at workplace includes physical ergonomic psychosocial interpersonal conflicts and administrative problems Workplace intervention is a rehabilitation program centred at the workplace allowing a graded transition from the clinical setting to the workplace Parallel with the workplace intervention the patients enter an exercise-program adjusted to the workplace intervention

The PREVICAP models have been evaluated in randomized controlled trials and has accelerated return to work by a factor 24 p001 The most important effect came from the workplace intervention which alone accelerated the return to work with a factor 19 p001 Patients randomized to the PREVICAP model had 60 days absence from work compared to 120 days in the control group

The PREVICAP model have been evaluated in Amsterdam by Dr Anema and he demonstrated a significant difference in the return to work rate between patients randomized to Workplace intervention and patients randomized to usual treatment

At the Back Clinic Ullevål University Hospital we have evaluated several exercise-programs with good effect on pain and function but not on the return to work rate This raises an important question will the return to work rate increase by including workplace intervention to the exercise program and it is possible to implement the PREVICAP model in Norway with the same good results despite differences between Canada The Netherlands and Norway with regard to culture soc-economic conditions working conditions and compensatory systems

We are planning to do a randomized controlled trial after the PREVICAP model where patients sick-listed for back pain will be randomized to either a workplace intervention plus an exercise-program or to an exercise-program alone

Purpose

The purpose of the project is to answer the following questions

1 Will more patients return to work and will they do it faster when they will be included in a work-related rehabilitations program than patients randomized to usual care by the general practitioner at the follow-up 6 weeks 3 months 6 months 1 and 2 years
2 Was there significant difference in pain and function between the two groups at the follow-up
3 Which factors predict the return to work medical socioeconomic or factors at the workplace
4 At the 2 years follow-up- Had the patients had episodes with back pain and in case how many of which duration and were they sick-listed for it or did they stay at work
5 Is there a favorable cost benefit with the program

The study is a prospective single-blind randomized study The patients will be randomized by block-randomisation The randomization will be carried out at a separate locations concealed from the clinical investigators

Inclusions criteria Patients with non-specific low back pain sick listed from 6-8 weeks and who are permanently employed Non-specific low back pain is defined as a back pain not attributable to a recognizable known specific pathology

Exclusions criteria Patients with infection tumors osteoporosis fracture structural deformity inflammatory disorder radicular syndrome or cauda equina syndrome spinal stenosis or spondylolysis listesis serious somatic disease andor psychic disease and patients with a poor proficiency in Norwegian

All patients will have a clinical examination of a specialist and a an exercise program The patients will be randomized to workplace intervention or a control group Patients randomized to the workplace intervention will be referred to an occupational ergonomist for work site evaluation and return to work program which include ergonomic conditions and relations to the employer and colleagues The occupational task of the ergonomists is to organize contacts and meetings between the employer and the patients and make a schedule for return to work Patients randomized to the control group will go back to their general practitioner for planning return to work

Sample sizeall together 260 patients in the study

Ethics The study will follow the ethic directions in the Helsinki Declaration and will not be initiated before approval from the National Committee for Research Ethics in Norway In addition we will also ask for permission to collect and register the data from the Data Inspectorate in Norway Only patients giving informed consent will be included and they will be informed that they can withdraw from the study at any time and that this will have no otherwise consequences for their treatment

Registrations of drop-outs The moment time and the cause of drop-outs will be registered We will attempt to obtain a clinical examination from drop-outs at the 1-year follow-up

Data analyses and statistic analyses All data will be anonymous coded and registered electronic i SPSS They will be unidentified in analyses and presentations

Parametric analyses will be applied on data which are normally distributed or else non-parametric statistic will be used Survival analyses will be used for investigating difference in reduction sickness leave between the two treatment groups Multivariate analyses will be used for identifying differences in pain function and fear of avoidance between the two groups In addition to analysing the data from the patients who completed the trial the data from dropouts will be analysed according to the intention-to-treat principle

Preconditions at the Back Clinic for conduction of the study The Back Clinic Ullevål University Hospital has collaboration with the Compensation system in Oslo NAV Norges Arbeids-og Velferdsetat The surplus from the Back Clinic will be used to employ an occupational ergonomist The physiotherapists are employees at the Back Clinic and they have tried out the exercise program Principal investigator Anne Keller is applying for grants for a post doc fellowship

The Back clinic has a test laboratory with a bicycle for testing submaximal oxygen uptake and inclinometer for measuring range of motion of flexion of the back We have collaboration with Department of neuroradiology for MRI investigations

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None