PREPARE: Pre-surgery physiotherapy for patients with degenerative lumbar spine disorder: a randomized controlled trial protocol
© The Author(s). 2016
Received: 27 February 2016
Accepted: 29 June 2016
Published: 11 July 2016
Current guidelines for the management of patients with specific low back pain pathology suggest non-surgical intervention as first-line treatment, but there is insufficient evidence to make recommendations of the content in the non-surgical intervention. Opinions regarding the dose of non-surgical intervention that should be trialled prior to decision making about surgery intervention vary. The aim of the present study is to investigate if physiotherapy administrated before surgery improves function, pain and health in patients with degenerative lumbar spine disorder scheduled for surgery. The patients are followed over two years. A secondary aim is to study what factors predict short and long term outcomes.
This study is a single blinded, 2-arm, randomized controlled trial with follow-up after the completion of pre-surgery intervention as well as 3, 12 and 24 months post-surgery. The study will recruit men and women, 25 to 80 years of age, scheduled for surgery due to; disc herniation, spinal stenosis, spondylolisthesis or degenerative disc disease. A total of 202 patients will be randomly allocated to a pre-surgery physiotherapy intervention or a waiting list group for 9 weeks. The waiting-list group will receive standardized information about surgery, post-surgical rehabilitation and advice to stay active. The pre-surgery physiotherapy group will receive physiotherapy 2 times per week, consisting of a stratified classification treatment, based on assessment findings. One of the following treatments will be selected; a) Specific exercises and mobilization, b) Motor control exercises or c) Traction. The pre-surgery physiotherapy group will also be prescribed a tailor-made general supervised exercise program. The physiotherapist will use a behavioral approach aimed at reducing patient fear avoidance and increasing activity levels. They will also receive standardized information about surgery, post-surgical rehabilitation and advice to stay active. Primary outcome measure is Oswestry Disability Index. Secondary outcome measures are the visual analogue scale for back and leg pain, pain drawing, health related quality of life, Hospital anxiety and depression scale, Fear avoidance beliefs questionnaire, Self-efficacy scale and Work Ability Index.
The study findings will help improve the treatment of patients with degenerative lumbar spine disorder scheduled for surgery.
KeywordsLow back pain Physiotherapy Stratification Surgery Function
Low back pain (LBP) have a lifetime prevalence to up to 84 % and is a major cause of disability with substantial socioeconomic impact globally . The highest prevalence is in age-group 45–64 and many experience functional impairments and activity limitations. Up to 85 % of LBP is considered to have non-specific etiology  when the mechanism for LBP cannot be clearly identified. LBP can be the product of nociception from lumbar spine structures  or even the result of centrally mediated pain in the absence of nociception . Different LBP related pathologies can coexist but approximately 5 % of those receive a primary diagnosis of disc herniation , 3–4 % spinal stenosis  and lower number with spondylolisthesis and degenerative disc disease (DDD). In Swedish Spine register of spinal surgery patients these diagnoses are concluded as degenerative lumbar spine disorders .
Guidelines published internationally focusing on the management of LBP in primary care recommend screening for serious pathology, neurological symptoms, the consideration of psychosocial risk factors if there is no improvement and to avoid routine imaging for non-specific LBP . The prevalence of serious pathology in the form of malignancy, spinal fracture, infection, or cauda equine syndrome requiring referral to secondary or tertiary medical care occurs in only <1–4 % of primary health care LBP cases [9–11]. Guidelines recommend a multicomponent strategy for patients with longstanding LBP including supervised exercises and behavioral approach based on the presence of yellow flags .
Consistencies in the patient’s history, physical assessment, clinical tests and medical imaging may strengthen suspicion of specific pathologies such as disc-herniation, spinal stenosis, spondylolisthesis and DDD causing LBP [12–15]. In the absence of serious pathology, disc herniation usually has a good prognosis and non-surgical intervention is recommended 8–12 weeks before decision-making about surgery [16–18]. Leg pain intensity is a significant prognostic factor for subsequent surgery after non-surgical intervention . A recent overview of the literature suggests that surgery leads to short-term benefits for leg pain and to a lesser extent for LBP when compared with non-surgical treatment. Despite this, no short-term and long term effects have been observed for functional outcome measures . It is also uncertain if surgical intervention has positive or negative effects on the underlying disc disease in a longer perspective . In disc herniation, similar results have been observed for non-surgical and surgical intervention at one [5, 18] and two years follow-up , which supports the view that the non-surgical intervention should be thoroughly tested before decision making about surgery.
In mild to moderately symptomatic degenerative lumbar stenosis, the prognosis can be favorable in up to half of patients and non-surgical intervention is recommended before decision-making about surgery . However, a recent Cochrane review suggests that, high quality studies are needed to inform future evidence based guidelines about the content of the non-surgical intervention . The prevalence of spinal stenosis is increasing and therefore high quality research its management is of importance . In the older population spinal stenosis is the most common reason for spinal surgery. Surgical intervention is recommended in moderate to severe spinal stenosis , but up to 35 % of the patients remain doubtful or dissatisfied with the result of surgery .
Current guidelines for the management of degenerative lumbar spondylolisthesis suggest that when there is a predominance of stenotic radicular symptoms, treatment should be similar to treatment for symptomatic degenerative lumbar spinal stenosis . Therefore, surgical intervention is recommended when symptomatic spinal stenosis associated with low grade degenerative lumbar spondylolisthesis is recalcitrant to trial of non-surgical intervention . There is currently a limited evidence base comparing the two interventions for spondylolisthesis suggesting surgical intervention to be more successful than non-surgical intervention for pain and functional outcomes .
In patients with DDD, both non-surgical and surgical interventions have limited evidence . In a review of systematic reviews and RCTs, Jacobs et al  reported that for DDD, surgery is no more effective than high-intensity non-surgical interventions for improvements in pain scores or function. Similarly, a recent systematic review and meta-analysis suggests that there is strong evidence that lumbar fusion surgery is not more effective than non-surgical interventions in reducing disability because of chronic LBP .
Previous literature on the treatment of LBP has often been based on generic treatments for patients with heterogeneous body functional impairments and activity limitations. This may explain the small effect sizes reported in clinical trials . Recently attention has shifted to the homogenous classification of patients based on functional impairments and activity limitations with the aim of improving the effectiveness of individualized treatments . This has led to a focus on stratified care for LBP in the area of physiotherapy . One of these stratification care models is the Treatment Based Classification (TBC), using criteria from the subjective and physical assessment to classify patients to different treatment classifications . TBC has shown better treatment outcome than treatment according to guidelines in acute LBP , but this effect has not been found in patients with long-lasting non-specific LBP .
High quality evidence-based guidelines for the non-surgical intervention of these degenerative lumbar spine disorders are lacking. The optimal duration of non-surgical intervention before surgical intervention is considered unclear. For those patients selected for surgical intervention, there is currently a small body of literature suggesting that pre-surgery physiotherapy improves the outcome of spinal surgery [29, 30]. Nielsen et al showed that supervised home exercise to improve trunk muscle strength and cardiovascular conditioning gave better post-operatively functionality, faster recovery and shorter hospital stay. The patients reported higher level of satisfaction in the intervention group . Louw et al tested the effect of pre-surgery education, which showed lower health care consumption and a more favorable surgical experience . No study has tested a more comprehensive exercise program pre-surgery. In hip pathology, physiotherapy prior to joint replacement surgery has been shown to reduce pain and improve physical function in preparation for surgery . The extent to which patients have access to non-surgical intervention prior to decision-making about surgery is also lacking in the literature. Only 10 % of the clinical studies about the effect of surgery have information about non-surgical intervention prior to surgery for spinal stenosis . We hypothesize that supervised exercises that have been proposed for non-specific LBP combined with a TBC could be effective also for patients awaiting elective surgery. The prognosis of LBP is multifactorial and therefore it is of interest to understand other factors apart from pre-habilitation that can influence short- and long term outcome.
The aim is to investigate if physiotherapy administrated before surgery improves function, pain and health in patients with degenerative lumbar spine disorder scheduled for surgery. The patients are followed over two years. A secondary aim is to study what factors predict short and long term outcomes.
This study protocol describes a single blinded, 2-arm, randomized controlled trial with 2 year follow up and the 1 year follow up as primary end point. The protocol conforms to the SPIRIT 2013 recommendations.
A total of 202 consecutively selected patients will be included in the study. All patients are referred to the Spine Clinic at the University Hospital in Linkoping, Sweden. Individuals that fulfil the inclusion criteria will be asked to participate. After signed informed consent has been obtained, baseline measurement will be collected and randomisation will take place.
Inclusion criteria; Males and females aged 25–80 years that are scheduled for surgery with degenerative lumbar spine disorder; presence of low back and/or leg pain due to disc herniation, spinal stenosis, spondylolisthesis (Grade 4), degenerative disc disease (DDD); diagnosis confirmed by magnetic resonance imaging; pain level high enough to indicate surgical intervention; fluent in Swedish.
Exclusion criteria: Patients that are in need of acute surgery; have severe spinal pathology (such as osteoporosis, or fusion > 4 levels (5 vertebras) or other severe diagnoses; patients in need of re-surgery on the same level.
Pre-surgery waiting list group
Patients will receive standardized information about surgery from an orthopedic surgeon, post-surgery rehabilitation and advice to stay active.
Pre-surgery physiotherapy group
Active physiotherapy according to a TBC; a) Specific exercises and mobilization, or b) Motor control exercises or c) Traction.
Tailor-made general supervised exercise program.
Behavioral approach to reduce fear avoidance and increase activity level.
Patients will also receive standardized information about surgery from an orthopedic surgeon, post-surgery rehabilitation and advice to stay active.
Components of the two intervention protocol used in the trial
Waiting list group
Pre-surgery physiotherapy group
1a. Specific movement and mobilisation
- Mechanical loading strategies; repeated movements according to directional preference, mobilisation, and integration in a functional restoration program.
1b. Motor control exercise
- Exercise focused on trunk and pelvic floor muscle activation and integration in a functional restoration program
- Manual Traction producing symptom reduction
2. Tailor-made general supervised exercise program
- Individualised prescription (type of exercise and load) of aerobic, resistance, flexibility exercises with information documents and checklist for treatment, progression and dosage
3. Behavioral approach:
- Goal setting (establishment and regular reviews)
- Strategies to minimize barriers to goal attainment, for example education regarding; ergonomics, postural alignment, patho-anatomical/physiological explanation
- Self-mediated home exercise and physical activities (logbook)
Advice regarding general physical activity recommendations
Education regarding surgery
Education regarding post-surgical rehabilitation
All questionnaire based outcome measures will be performed at baseline, before surgery (after pre-surgery physiotherapy or waiting-list), as well as three months, one and two years after surgery. Two written reminders and if needed one telephone call will be used to enhance response rate. Subjective, physical assessment measures and TBC will be collected at baseline and after completion of the 9 weeks’ intervention.
Primary outcome measure
The primary outcome measure will be patient self-reported function and activity limitation measured by Oswestry Disability Index (ODI) . ODI contains ten items investigating pain related function impairment and activity limitations with six answer alternatives for each item. The sum score is between 0-100 %, with higher values representing higher functional disability score .
Secondary outcome measures
Pain will be evaluated with VAS , pain drawing and pain duration . Health related quality of life will be evaluated with SF-36  and EQ-5D . Anxiety and depression will be evaluated with the Hospital Anxiety and Depression Scale (HADS)  and self-efficacy with Self-efficacy scale (SES) . Fear avoidance will be measured by Fear avoidance belief questionnaire (FABQ) . Work will be assessed by general information of work and Work Ability Index (WAI) . Patient reported treatment effects will be measured by Patient reported global treatment effects and patient enablement instrument (PEI) . Expectations, sick-leave, lifestyle behavior, previous healthcare consumption and adverse events will also be measured. Patients randomized to pre-surgical physiotherapy will be evaluated with the Patient Specific Functional Scale (PSFS)  three times during the intervention. Subjective, physical assessment measures and TBC will be used as secondary outcome measures.
Based on a minimally clinical important change of 10 % on the ODI , a standard deviation for the ODI =20, a significance level of p = 0.05, a power of 80 %, an estimated 64 patients are required in each of the intervention groups, at the primary endpoint. The current sample size of 202 patients allows for a 35 % loss to follow-up while maintaining >80 % statistical power.
Block randomization will be used with smaller block size at the end of the study. Initially two blocks of 60 will be created and then subsequent blocks of 20, 8 and 4. For each randomization block, sealed opaque envelopes will be prepared with a 1:1 ratio of allocation to the pre-surgery waiting list group as well as the pre-surgery physiotherapy group. After baseline measurement, an independent physiotherapist working at the Spine Clinic will open a sealed opaque randomization envelope and inform the patient about group allocation. The same physiotherapist will contact the physiotherapy center where the patient will receive treatment.
The physiotherapist performing the clinical measures and assigning a treatment based classification will be blinded to the randomization, while patients and the physiotherapists treating the patients cannot be blinded.
Data collection methods
Clinical tests and TBC procedure
Baseline subjective and physical assessment measures will be assessed by a physiotherapist. The same assessment will be conducted at follow up after the intervention. The subjective assessment will include information on symptom duration, prior LBP, distribution of symptoms, symptom aggravating and easing positions (sitting, standing or walking), time tolerated in positions (sit, stand and walk) as well as signs of centrally disturbed pain modulation. Physical assessment will include test for aberrant movements, neurological tests (myotomes, dermatomes and reflexes) for spinal segmental levels L4-S1, straight leg raising, range of motion for internal rotation of hips, posterior-anterior-test lumbar segmental provocation test (PA-test), Sacroiliac joint provocation tests (SI-tests), test for symptom centralization, prone instability test, active straight leg raise (A-SLR), Trendelenburg test, isometric bilateral quadriceps strength and 10 m walking-test [46, 47].
Data will be stored at the research department at Linköping University, not allowing for identification for individuals.
Data collected at the longitudinal time points will be analysed according to the ‘intention to treat’ (ITT) principle. Data analysis according to ITT requires that data for every patient, regardless of level of intervention compliance, data missing at follow-up or due to drop-out, will be included in the group to which they are randomised . To perform an ITT analysis, missing data will be replaced through multiple imputation methods. In an attempt to determine the sensitivity of the ITT data, it will be compared to per-protocol data from patients who have complied with the original study protocol. Alternative analyses will also be performed to take treatment compliance into consideration. Analysis of variance ANOVA will be used to investigate within and between group differences in longitudinal outcome measures. Within and between group Cohens d effect sizes will also be calculated. Multivariate regression will be used to analyse potential predictors of long term outcomes.
In degenerative lumbar spine disorders the outcome after surgery is questioned since about 20–35 % are doubtful or dissatisfied with the results at one year follow up . Few studies have used physiotherapy as a preparation before surgery, one with information and one with home exercise program that improved patient reported outcome and healthcare consumption [29, 30]. The question still remains if more comprehensive physiotherapy intervention will change the short- and long term outcome. In this study we target several dimensions in the biopsychosocial model. It is known that there is a risk that patients with persistent pain develop fear avoidance and maladaptive pain behavior, deterioration in physical performance and inactivity. In contrast to previous studies the strategy is based on the TBC and tailor-made exercise program. This does not allow to study single interventions. The strength is to introduce a standardized assessment for this patient group that can be part of a clinical reasoning process.
The design includes a broad assessment that will make it possible to look for predictive factors in this heterogeneous population supporting a better risk assessment of good or poor outcome.
A limitation of the study is that the treatments cannot be blinded to patient and treatment provider. The generalizability of the study’s results may be affected by the process of selecting patients for surgery which might be different in different countries and health care systems. Another limitation might be that all patients will be informed that they are scheduled for surgery, which could influence their expectations and attitudes towards pre-surgery-physiotherapy and bias self-reported outcome.
The trial is ongoing and the final two-year follow-up will be finished November 2018.
This study uses a randomized controlled design to investigate if pre-surgery physiotherapy improves function, pain and health in patients with degenerative lumbar spine disorder before and after surgery. The study will also investigate what factors predict short and long term outcomes. The novel findings will contribute to evidence-based recommendations as to the effect of stratified pre-surgery physiotherapy in patients with degenerative lumbar spine disorder scheduled for surgery. Furthermore, findings will provide direction for future research.
The project is funded by the Faculty of Medicine and Health, Linköping University and NHS FoU fond, County Council of Östergötland.
Availability of data and materials
As this is a study protocol, no data are presented.
YL P, and BÖ conceived the project and are leading the co-ordination of the trial. BÖ procured project funding. YL, HT, PE, AA and BÖ contributed to the protocol design and provided feedback on drafts of this manuscript and have read and approved the final paper.
The authors have no competing interests to declare.
Consent for publication
Ethics approval and consent to participate
The trial has received ethical approval from the Regional Ethics Committee in Linköping (Dnr 2012/167-31), approved 2012-05-23. The patients will sign informed consent before baseline measurement and randomisation.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Balague F, Mannion AF, Pellise F, Cedraschi C. Non-specific low back pain. Lancet. 2012;379(9814):482–91.View ArticlePubMedGoogle Scholar
- Deyo RA, Rainville J, Kent DL. What can the history and physical examination tell us about low back pain? JAMA. 1992;268:760–5.View ArticlePubMedGoogle Scholar
- Cavanaugh JM. Neural mechanisms of lumbar pain. Spine. 1995;20(16):1804–9.View ArticlePubMedGoogle Scholar
- Melzack R. Katz J. Pain WIREs Cogn Sci. 2013;4:1–15.View ArticleGoogle Scholar
- Gibson JN, Waddell G. Surgical interventions for lumbar disc prolapse. Cochrane Database Syst Rev. 2007;1(1):CD001350.4.Google Scholar
- Whitman JM, Flynn TW, Childs JD, Wainner RS, Gill HE, Ryder MG, et al. A comparison between two physical therapy treatment programs for patients with lumbar spinal stenosis: A randomized clinical trial. Spine (Phila Pa 1976). 2006;31(22):2541–9.View ArticleGoogle Scholar
- Strömqvist B, Fritzell P, Hägg O, Jönsson B, Sandén B. Swespine: the Swedish spine register. The 2012 report. Eur Spine J. 2013;22:953–74.View ArticlePubMedPubMed CentralGoogle Scholar
- Koes BW, van Tulder M, Lin CW, Macedo LG, McAuley J, Maher C. An updated overview of clinical guidelines for the management of nonspecific low back pain in primary care. Eur Spine J. 2010;19:2075–94.View ArticlePubMedPubMed CentralGoogle Scholar
- Henschke N, Maher CG, Refshauge KM, Herbert RD, Cummings RG, Bleasel J, York J, Das A, McAuley JH. Prevalence of and screening for serious spinal pathology in patients presenting to primary care settings with acute low back pain. Arthritis Rheum. 2009;60(19):3072–80.View ArticlePubMedGoogle Scholar
- Williams CM, Henschke N, Maher CG, van Tulder MW, Koes BW, Macaskill P, Irwig L. Red flags to screen for vertebral fracture in patients presenting with low back pain. Cochrane Database Syst Rev. 2013;1:CD008643.Google Scholar
- Henschke N, Maher CG, Ostelo RW, de Vet HC, Macaskill P, Irwig L. Red flags to screen for malignancy in patients with low-back pain. Cochrane Database Syst Rev. 2013;2:CD008686.Google Scholar
- Shultz S, Averell K, Eickelman A, Sanker H, Burrowbridge Donaldson M. Diagnostic accuracy of self-report and subjective history in the diagnosis of low back pain with non-specific lower extremity symptoms: A systematic review. Manual Ther. 2015;20:18–27.View ArticleGoogle Scholar
- Cook C, Hegedus E. Diagnostic utility of clinical tests for spinal dysfunction. Manual Ther. 2011;16:21–5.View ArticleGoogle Scholar
- Wassenaar M, van Rijn RM, van Tulder MW, Verhagen AP, van der Windt DAWM, Koes BW, de Boer MR, Ginai AZ, Ostelo RWJG. Magnetic resonance imaging for diagnosing lumbar spinal pathology in adult patients with low back pain or sciatica: a diagnostic systematic review. Eur Spine J. 2012;21:220–7.View ArticlePubMedGoogle Scholar
- Raastad J, Reiman M, Coeytaux R, Ledbetter L, Goode AP. The association between lumbar spine radiographic features and low back pain: A systematic review and meta-analysis. Semin Arthritis Rheum. 2015;44(5):571–85.View ArticlePubMedGoogle Scholar
- Verwoerd AJH, Luijsterburg PAJ, Lin CWC, Jacobs WCH, Koes BW, Verhagen AP. Systematic review of prognostic factors predicting outcome in non-surgically treated patients with sciatica. Eur J Pain. 2013;17:1126–37.View ArticlePubMedGoogle Scholar
- Kreiner DS, Hwang SW, Easa JE, Resnick DK, Baisden JL, Bess S, Cho CH, DePalma MJ, Dougherty P 2nd, Fernand R, Ghiselli G, Hanna AS, Lamer T, Lisi AJ, Mazanec DJ, Meagher RJ, Nucci RC, Patel RD, Sembrano JN, Sharma AK, Summers JT, Taleghani CK, Tontz WL Jr, Toton JF, North American Spine Society. An evidence-based clinical guideline for the diagnosis and treatment of lumbar disc herniation with radiculopathy. Spine J. 2014;14(1):180–91.View ArticlePubMedGoogle Scholar
- Jacobs WC, Rubinstein SM, Willems PC, Moojen WA, Pellisé F, Oner CF, Peul WC, van Tulder MW. The evidence on surgical interventions for low back disorders, an overview of systematic reviews. Eur Spine J. 2013;22(9):1936–49.View ArticlePubMedPubMed CentralGoogle Scholar
- Kreiner DS, Shaffer WO, Baisden JL, Gilbert TJ, Summers JT, Toton JF, Hwang SW, Mendel RC, Reitman CA, North American Spine Society. An evidence-based clinical guideline for the diagnosis and treatment of degenerative lumbar spinal stenosis (update). Spine J. 2013;13(7):734–43.View ArticlePubMedGoogle Scholar
- Ammendolia C, Stuber KJ, Rok E, Rampersaud R, Kennedy CA, Pennick V, Steenstra IA, de Buin LK, Furlan AD. Nonoperative treatment for lumbar spinal stenosis with neurogenic claudication. Cochrane Database Syst Rev. 2013;8:CD010712.Google Scholar
- Watters 3rd WC, Bono CM, Gilbert TJ, Kreiner DS, Mazanec DJ, Shaffer WO, Baisden J, Easa JE, Fernand R, Ghiselli G, Heggeness MH, Mendel RC, O’Neill C, Reitman CA, Resnick DK, Summers JT, Timmons RB, Toton JF, North American Spine Society. An evidence-based clinical guideline for the diagnosis and treatment of degenerative lumbar spondylolisthesis. Spine J. 2009;9(7):609–14.View ArticlePubMedGoogle Scholar
- Garet M, Reiman MP, Mathers J, Sylvain J. Nonoperative treatment in lumbar spondylolysis and spondylolisthesis: a systematic review. Sports Health. 2013;5(3):225–32.View ArticlePubMedPubMed CentralGoogle Scholar
- Saltychev M, Eskola M, Laimi K. Lumbar fusion compared with conservative treatment in patients with chronic low back pain: a meta-analysis. Int J Rehab Res. 2014;37:2–8.View ArticleGoogle Scholar
- Foster NE. Barriers and progress in the treatment of low back pain. BMC Med. 2011;9:108.View ArticlePubMedPubMed CentralGoogle Scholar
- Foster NE, Hill JC, O’Sullivan P, Hancock M. Stratified models of care. Best Pract Res Clin Rheumatol. 2013;27:649–61.View ArticlePubMedGoogle Scholar
- Stanton TR, Fritz JM, Hancock MJ, Latimer J, Maher CG, Wand BM, Parent EC. Evaluation of a treatment-based classification algorithm for low back pain: A cross-sectional study. Phys Ther. 2011;91(4):496–509.View ArticlePubMedGoogle Scholar
- Fritz JM, Delitto A, Erhard RE. Comparison of classification-based physical therapy with therapy based on clinical practice guidelines for patients with acute low back pain: A randomized clinical trial. Spine. 2003;28(13):1363–72.PubMedGoogle Scholar
- Apeldoorn AT, Ostelo RW, van Helvoirt H, Fritz JM, Knol DL, van Tulder MW, et al. A randomized controlled trial on the effectiveness of a classification-based system for subacute and chronic low back pain. Spine. 2012;37(16):1347–56.View ArticlePubMedGoogle Scholar
- Nielsen PR, Jørgensen LD, Dahl B, Pedersen T, Tønnesen H. Prehabilitation and early rehabilitation after spinal surgery: randomized clinical trial. Clin Rehabil. 2010;24:137–48.View ArticlePubMedGoogle Scholar
- Louw A, Diener I, Landers MR, Puentedura EJ. Preoperative pain neuroscience education for lumbar radiculopathy: a multicenter randomized controlled trial with 1-year follow-up. Spine. 2014;39(18):1449–57.View ArticlePubMedGoogle Scholar
- Gill SD, McBurney H. Does exercise reduce pain and improve function before hip or knee replacement surgery? A systematic review and meta-analysis of randomized controlled trials. Arch Phys Med Rehabil. 2013;94:164–76.View ArticlePubMedGoogle Scholar
- ECRI Health Technology Assessment Group. Treatment of degenerative lumbar spinal stenosis. Evid Rep Technol Assess (Summ). 2001;32:1–5.Google Scholar
- Borg G. Psychophysical bases of perceived exertion. Med Sci Sports Exerc. 1982;14(5):377–81.View ArticlePubMedGoogle Scholar
- Fairbank JC, Couper J, Davies JB, O’Brien JP. The oswestry low back pain disability questionnaire. Physiotherapy. 1980;66(8):271–3.PubMedGoogle Scholar
- Scott J, Huskinsson EC. Graphic representation of pain. Pain. 1976;2:175–84.View ArticlePubMedGoogle Scholar
- Southerst D, Côté P, Stupar M, Stern P, Mior S. The reliability of body pain diagrams in the quantitative measurement of pain distribution and location in patients with musculoskeletal pain: a systematic review. J Manipulative Physiol Ther. 2013;36(7):450–9.View ArticlePubMedGoogle Scholar
- Aaronson NK, Acquadro C, Alonso J, Apolone G, Bucquet D, Bullinger M, Bungay K, Fukuhara S, Gandek B, Keller S, Razavi D. Sanson-Fisher FL, Sullivan M, Wood-Dauphinee S, Wagner A, Ware JE. International quality of life assessment (IQOLA) Project. Qual Life Res. 1992;1:349–51.View ArticlePubMedGoogle Scholar
- The EuroQol Group. EuroQol-a new facility for the measurement of health-related quality of life. Health Policy. 1990;16(3):199–208.View ArticleGoogle Scholar
- Zigmond AS, Snaith RP. The hospital anxiety and depression scale. Acta Psychiatr Scan. 1983;67(6):361–70.View ArticleGoogle Scholar
- Altmaier EM, Lehmann TR, Russell DW, Weinstein JN, Kao CF. The effectiveness of psychological interventions for the rehabilitation of low back pain: a randomized controlled trial evaluation. Pain. 1992;49:329–35.View ArticlePubMedGoogle Scholar
- Waddel G, Newton M, Henderson I, Somerville D, Main CJ. A Fear-Avoidance Beliefs Questionnaire (FABQ) and the role of fear-avoidance beliefs in chronic low back pain and disability. Pain. 1993;52(2):157–68.View ArticleGoogle Scholar
- de Zwart BC, Frings-Dresen MH, van Duivenbooden JC. Test-retest reliability of the Work Ability index questionnaire. Occup Med. 2002;52(4):177–81.View ArticleGoogle Scholar
- Howie JG, Heaney DJ, Maxwell M, Walker JJ. A comparison of a Patient Enablement Instrument (PEI) against two established satisfaction scales as an outcome measure of primary care consultations. Fam Pract. 1998;15(2):165–71.View ArticlePubMedGoogle Scholar
- Stratford P, Gill C, Westaway M, Binkley J. Assessing disability and change on individual patients: a report of a patient specific measure. Physiother Can. 1995;47:258–63.View ArticleGoogle Scholar
- Hägg O, Fritzell P, Nordwall A. The clinical importance of changes in outcome scores after treatment for chronic low back pain. Eur Spine J. 2003;12:12–20.PubMedGoogle Scholar
- Larsson LE, Odenrick P, Sandlund B, Weitz P, Oberg PA. The phases of the stride and their interaction in human gait. Scand J Rehabil Med. 1980;12(3):107–12.PubMedGoogle Scholar
- Odenrick P. On analysis and clinical measurement of gait and upright stance. Clin Biomechanics. 1988;3:222–4.View ArticleGoogle Scholar
- Albert HB, Hauge E, Manniche C. Centralization in patients with sciatica: are pain responses to repeated movement and positioning associated with outcome or types of disc lesions? Eur Spine. 2012;21(4):630–6.View ArticleGoogle Scholar
- Schneider M, Erhard R, PT, Brach J, PT, Tellin W, Imbarlina F, Delitto A. Spinal palpation for lumbar segmental mobility and pain provocation: an interexaminer reliability study. J Manipulative Physiol Ther. 2008; 6:465–473.Google Scholar
- Hollis S, Campbell F. What is meant by intention to treat analysis? Survey of published randomised controlled trials. BMJ. 1999;319(7211):670–4.View ArticlePubMedPubMed CentralGoogle Scholar