BACKGROUND: Several treatments exist for chronic low back pain (cLBP) patients although none has shown superiority. Among group treatments, muscle reconditioning programmes (MRPs) are the most commonly used. Multidisciplinary functional rehabilitation programmes (MFRPs) are an alternative.
OBJECTIVE: To compare a MFRP with a MRP as few studies compare these treatments
METHODS: This was a prospective, nonrandomised, controlled study comparing cLBP patients participating in a MRP or MFRP in an outpatient setting. The predetermined primary outcome measure was the daily life activity subscale (DLA) of the Dallas Pain Questionnaire (DPQ) within one year after the end of the treatment.
RESULTS: Twenty-one patients were included in the MRP and 24 in the MFRP. At inclusion, the groups were similar in terms of age (mean 40 years), sex (50%–60% males), sick leave duration (mean 6.0 months, standard deviation (SD) 4.4 months) and follow up (mean 9.0 months, SD 2.0 months). The DLA score decreased from 59.5% (SD 16.9) to 44.8% (SD 25.4), p <0.01, in the MFRP and from 62.3 (SD 20.3) to 58.8 (SD 20.7), p = 0.3, in the MRP. The between-groups difference at follow-up was 13.8, p = 0.05, and the difference in the mean improvement was –11.5 (5.9), p = 0.058. Seventy-eight percent of MFRP patients versus 47 % in the MRP group returned to work (p = 0.08).
DISCUSSION: In a population of highly disabled cLBP patients, MFRP seems more effective in increasing function and return to work. Interpretation is limited by the small population included and by the type of trial.
CONCLUSION: Randomised studies are needed to confirm these results and explore the cost-effectiveness of MFRP.
Keywords: low back pain, multidisciplinary functional rehabilitation, muscular rehabilitation, daily life activity, cognitive behavioural treatment
Non-specific low back pain (LBP) is a major public health problem. Overall, 60%‑80% of the population will be affected by this problem at least once in their lifetime [1, 2]. The majority will recover favourably and return to a normal active life within a few weeks without consequences. Seven to ten percent will develop a chronic condition (pain lasting >3 months ) associated with numerous incapacities in daily life . For these patients, several therapeutic approaches have been developed. These can be basically classified into two groups. One group includes treatments focusing on muscle reconditioning through exercises. Benefits of these treatments on pain and function have been reported for the short term [5, 6], but the effect on return to work is less clear [5, 7]. The second group includes cognitive behavioural treatments, based on the theory and observations that avoidance behaviour and inappropriate beliefs are major factors in the development of chronicity. Treatments based on these theories have a moderate effect on pain, function and behaviour [8–10]. The addition of a cognitive component to physical approaches has been rather disappointing [11–13]. More complex multidisciplinary treatments integrating physical rehabilitation, psychological evaluation, cognitive behavioural methods and occupational therapy with a socioprofessional component are frequently advocated , but there is a lack of studies directly comparing these complex approaches with simpler muscle reconditioning programmes (MRPs).
The development of an outpatient multidisciplinary functional rehabilitation program (MFRP) to replace a more traditional outpatient MRP gave us the opportunity to compare these two approaches.
Aim of the study
The aim of the study was to compare MRP with MFRP in order to evaluate their respective efficacies and to explore the potential additional value of the more complex intervention.
|Table 1: Content of the programmes.|
|Multidisciplinary functional rehabilitation programme||Muscle reconditioning programme|
|Number patients per group||4–6||4–6|
|Hours per day||5||3|
|Total number of hours||97*||46|
|Group physiotherapy, hours||46||40|
|Unsupervised exercises, hours||20**|
|Occupational therapy, hours||7||6|
|Analytic group therapy, hours||4|
|Patient education session, hours||12|
|Workplace evaluation||yes (optional)||no|
|Individualised treatment goals||yes||no|
|* This figure includes welcoming and closing sessions, individual biopsychosocial evaluation, goal setting and restitution sessions for a total of 8 hours|
** Only for patients who cannot go back to work part time during week 3 and 4 of the programme.
This was a prospective nonrandomised controlled study comparing patients with chronic low back pain (cLBP) participating in a group programme based on intensive physical exercises (MRP) with similar patients participating in a multidisciplinary rehabilitation programme (MFRP). Patients with recurrent episodes of low back pain for more than four weeks within the same year were considered chronic and could also be included. This study was conducted on the occasion of a change in treatment strategy in our institution, with MFRP replacing MRP. The data were collected from mid-2006 to mid-2007 for MRP and from the end of 2007 to 2008 for MFRP. All patients were recruited at the tertiary rheumatology and rehabilitation centre of Geneva University Hospitals with strictly identical eligibility criteria. To be included, patients had to be 18 to 65 years old, suffering from non-specific low back pain (with or without radiating leg pain) despite standard care from their general practitioner, including pain medication and individual physiotherapy. Patients working outside the home had to be on sick leave. A good understanding of spoken and written French was also required. Exclusion criteria were specific low back pain due to infection, tumour, spondylarthropathy, radicular leg pain due to disc herniation and neurogenic claudication related to spinal stenosis. Patients suffering from medical comorbidities that could interfere or prohibit their participation (e.g. cardiac or pulmonary failure, severe mood disorder, disabling knee osteoarthritis) or with a diffuse chronic pain syndrome were also excluded. Patients on sick leave for more than two years or receiving a disability pension were likewise excluded. All eligible patients who consulted at the rheumatology and rehabilitation centre were included unless the programme was full. In this case, the patient was included in the next programme session. Whilst in the study, pain medication was adapted as needed but physiotherapy outside the programme was interrupted.
The MRP was designed to increase musculoskeletal strength and endurance and to teach basic knowledge of ergonomics. It was held for groups of four to six participants, five half-days/week over three weeks, providing a total of 45 hours of physical therapy with muscle reinforcement and stabilisation exercises, relaxation, proprioception sessions and water gymnastics. Six hours of occupational therapy focusing on prespecified activities (sitting, lifting, handling and driving) were provided. No individualisation of therapy during the sessions was offered (table 1).
The MFRP was designed to restore the individual’s musculoskeletal function and included significant cognitive behavioural components and work-related goals and outcomes [15, 16]. It was designed by an extensive multidisciplinary team (rheumatologist, rehabilitation physician, pain specialist, psychiatrist, physical therapists, occupational therapists and a psychologist) for groups of four to six patients, and was held over four weeks for a total of 100 hours (table 1). A complete description of the methods used to devise the programme has been published [17, 18]. All treatments were delivered in groups, but the type and intensity of the physical treatment were tailored to each patient, based on an initial evaluation of his/her physical capacities, psychosocial impairments, expectations and priorities. Most importantly, personalised, realistic and measurable objectives were defined individually at the beginning of the programme and reassessed in the end. Treatments sessions included: (1.) cardiorespiratory fitness, muscular strength, muscular flexibility, stabilisation exercises, relaxation, proprioception and water gymnastics; (2.) occupational therapy with emphasis on individual professional and daily life situations; (3.) patient education sessions based on a noninjury model [19, 20] and the biopsychosocial model; and (4.) one hour per week of support group discussion led by a psychiatrist (table 1). The programme was designed to increase muscle activities progressively and to help the patients overcome their fear of movement whenever fear avoidance beliefs were detected during initial evaluation. Alongside the programme, patients developed their own booklet of illustrated and annotated exercises and techniques that they found appropriate for their condition. Return to work during the mornings of the third or the fourth week was encouraged when possible. If not working, patients had to come each morning to the site to perform two hours of unsupervised exercises, as taught during the first weeks.
The main outcome measure was the French validated version of the Dallas Pain Questionnaire (DPQ), as it is the only self-administered questionnaire developed according to the biopsychosocial model of cLBP . It explores four different dimensions (daily life activities, work-leisure, anxiety-depression and sociability) in 16 questions, each dimension having between three and seven questions. The answer to each question is recorded on a Likert scale and computed so that each dimension has a final score ranging from 0% to 100%, where 0% is best. Pain was evaluated on a visual analogue scale (VAS) from 0–10. Work ability at follow up was defined as being at work or having the ability to be at the workplace (e.g. an unemployed patient without sickness leave). For both types of treatment, data were collected prior to the programme and a questionnaire was mailed six to eight months after its conclusion. In addition to pain and the DPQ, return to work was also assessed. The data were collected from mid-2006 to mid-2007 for the MRP and from the end of 2007 to 2008 for the MFRP, at the tertiary rheumatology and rehabilitation centre of Geneva University Hospital.
Distribution of the variables was checked for normality using normality plots and by determining skewness and kurtosis. Within-groups comparisons were made with paired Student t-tests, between-groups comparisons were made with unpaired Student t-tests for normally distributed variables and a non-parametric test (Mann-Whitney U test) was used when this assumption was not satisfied. Analysis was performed using STATA version 11 for Windows (StataCorp).
|Table 2: Baseline characteristics of the study population.|
|Multidisciplinary functional rehabilitation programme
(n = 24)
|Muscle reconditioning programme
(n = 21)
|Age (years), mean (SD)||39.9 (11.7)||41.1 (10.9)||NS|
|Sex (male), n (%)||14 (58.3)||10 (47.6)||NS|
|Length of follow up (months), mean (SD)||8.7 (2.9)||8.8 (1.2)||NS|
|Length of sick leave (months), mean (SD)||6.0 (4.4)||5.1 (4.7)||NS|
|Type of work, n (%)|
| 3 (13)|
| 5 (24) |
|Length of the present episode (months), n (%)|
| 3 (13)|
| 5 (24)|
|Pain (VAS 0‑100), mean (SD)||59.3 (16.3)||59.0 (20.4)||NS|
|Dallas Pain Questionnaire (0–100), mean (SD)|
daily life activity
|SD = standard deviation; NS = not significant|
Twenty-one patients were included in the MRP group and 24 in the MFRP group. The MRP patients had a subsequent evaluation after 8.8 (standard deviation (SD) 1.2) months, the MFRP group after 8.7 (SD 2.9) months. The main sociodemographic and clinical data are presented in table 2.
Muscle reconditioning program (MRP)
Mean (SD) values were decreased in three out of the four subscales of the DPQ: ‘daily life activity’ (62.3 (20.3) vs 58.8 (20.7)), ‘work-leisure’ (65.5 (23.1) vs 56.4 (24.4) and ‘anxiety-depression’ (45.2 (26.9) vs 40.0 (24.89)). None of these differences was statistically significant, although a trend was observed for ‘work-leisure’ (-9.1 (22.0), 95% confidence interval (CI) –19.4–1.2, p = 0.08). There was no effect on the social interest subscale (39.5 (24.3) vs 39.0 (26.5)). Pain score on the VAS decreased from 5.9 (2.0) to 5.1 (2.7), (–0.8 (2.7), 95% CI –2.1–0.4, p = 0.19). Out of the 21 patients, work ability outside the home at follow up could be assessed in 17 (three housewives and one early retirement). All were on sick leave at inclusion and eight (47%) were working at follow up.
Multidisciplinary functional restoration program (MFRP)
Mean (SD) values were statistically improved for the ‘daily life activity’ (59.5 (16.9) vs 44.8 (25.4), p = 0.002) and ‘work-leisure’ (61.0 (24.3) vs 42.2 (29.4), p = 0.001) subscales of the DPQ. There was no significant difference for the ‘anxiety-depression’ (51.8 (28.8) vs 46.6 (30.7), p = 0.5) and ‘sociability’ (38.3 (24.3) vs 38.5 (24.9)) subscales. The pain score on the VAS decreased significantly from 5.9 (1.6) to 4.5 (2.4), p = 0.01. Out of the 24 patients, work ability at follow up could be assessed in 23 (the other was a housewife). All were on sick leave at inclusion and 18 (78%) were working at follow up.
Between group comparison
There was no significant difference at inclusion on the DPQ subscales or in pain. Mean scores on the ‘daily life activity’ subscale of the DPQ at follow up were better in the MFRP group than in the MRP group (44.8 (25.4) vs 58.6 (20.2), respectively), with a mean difference of 13.8 (6.9), p = 0.05. The difference in the mean improvement was –11.5 (5.9), 95% CI –23.5–0.4, p = 0.058. A similar result was observed for the ‘work-leisure’ subscale: 42.3 (29.4) vs 56.6 (23.8), difference in the mean improvement –11.1 (6.9), 95%CI–25.1–2.9, p = 0.11. The other two subscales and the pain scores showed no between-group differences (fig. 1). Rate of return to work among patients with work ability was higher in the MFRP group, without reaching statistical significance (78% vs 47%, p = 0.08).
The main goal of the study was to compare the effect of an intensive multidisciplinary rehabilitation programme with that of a muscle reconditioning programme on biopsychosocial consequences of chronic low back pain as measured by the DPQ. With the MFRP significant improvement was observed in the daily life activity and leisure-work subscales of the DPQ, as well as in pain on the VAS. The difference for the primary endpoint (DPQ daily life activity) reached the threshold of a 30% improvement, which is recommended as a clinically relevant improvement . No such improvement was observed with the MRP. When comparing both programmes, a notable difference in absolute values was observed for these dimensions, however there was a statistical difference only in favour of MFRP. The same effect was observed for return to work, with a 40% increase in the work ability rate in the MFRP group as compared with the MRP group, but statistically a difference in favour only of the more complex programme. No impact was measured on the other DPQ subscales.
Although MRP is recommended for the treatment of cLBP , the group of patients receiving this treatment showed only a nonsignificant modest effect. This observation could have resulted from the high degree of functional impairment in this population, which was reflected by the high scores in all DPQ subscales as compared with the usual reports from similar studies [23, 24]. In fact, these scores were at levels comparable to those reported in surgical studies [25–27]. Hence, in this population of highly disabled patients, we hypothesise that straightforward MRP is less effective and that the implementation of a complex multidimensional programme is needed in order to observe a significant effect on function and a substantial increase in the rate of return to work.
This study directly compared, in a similar outpatient setting, two kinds of group therapy based on exercises, and found evidence of greater effectiveness with MFRP as compared with MRP. According to recent reviews, there is no randomised controlled trial that directly compared these two interventions [28, 29]. The superiority of intensive MFPR in an outpatient setting has been mainly compared with usual care , passive physiotherapy  or a less intensive multidisciplinary programme ; when compared to active individual therapy the difference was either modest [24, 32] or nonsignificant . In a different approach, other authors have looked at the effect of adding cognitive behavioural treatment (CBT) to a physical programme and failed to demonstrate an additional effect [10–12].
There are several important differences that could explain the positive results we observed in this study. Firstly, this programme was not designed as a CBT treatment. Principles of CBT were taught to the entire team and the team was encouraged to emphasise the use of personalised objectives within the group sessions in order to adapt the rhythm of progression and to increase motivation and satisfaction, factors known to positively influence pain and function [33–35]. A similar approach has recently been shown to be successful in a large randomised controlled trial performed in a setting of individual physiotherapy . Secondly, interventions were based on a noninjury theory model [19, 37] and this model was introduced to the patients in specific sessions using therapeutic education principles. Classically cLBP is considered to be the consequence of repetitive microinjury of the spine and subsequent muscle deconditioning. This hypothesis has been recently challenged  and the alternative noninjury model has been proposed . The implementation of this model in different settings has been shown to have a favourable impact on cLBP [20, 37]. Finally, workplace assessment was also included. Structured intervention at the workplace has shown positive impact on return to work or reduction of sick leave days [39, 40]. In our country, this kind of intervention is extremely difficult to set up and not well accepted by the employers, even when it is integrated into an institutional intervention such as for this programme. Although a thoughtful assessment of the work situation was included for all participants, we could conduct interventions at the workplace for only a fraction of them. Hence the real impact of this part of our intervention on the overall results remains to be proven.
The absence of change on the “anxiety-depression” and the “sociability” subscales of the DPQ was not anticipated. These complex problems might be difficult to modify even with a four-week multidisciplinary rehabilitation programme. The absence of effect has been reported by others [10, 31, 41–43]. Other studies did show an effect , but their populations had a 10% lower score on the DPQ scales at inclusion compared with our patients, and were referred for individual psychological evaluation and treatment when needed. This illustrates the difficulty of addressing these complex issues in a group programme, and identifies a possible obstacle to better results with extensive and costly multidisciplinary programs for cLB patients.
The main limitations of the present results are due to the nonrandomised design. Despite the abundant literature on back pain, to the best of our knowledge no higher quality evidence has been published on this specific topic. Running two demanding programmes at the same time within the same institution was impossible in terms of logistics. In order to have comparable populations, great care was taken not to modify eligibility criteria. This is reflected by the similarity of the two populations at inclusion (table 2). However we acknowledge that by doing so we were not able to completely rule out confounders such as differences in treatments during the follow-up time. The interpretation of the results is also limited by the small sample size which explains the fact that although MFRP showed a much greater effect in absolute values, the difference between MFRP and MRP was just at the threshold of significance. Post hoc analysis revealed that in the present setting we had only a 50% chance of reaching a statistically significant result. If anything, the efficacy of the MFRP was rather underestimated as the team had to acquire new competencies in the field of CBT and it took several months to be at ease with these concepts. The main reason for the superiority of MFPR over MRP could be attributed to the increasing amount of hours of treatment delivered by the therapists in the MFPR. However, as shown in table 1, most of the increased time in the MFPR, as compared with MRP, was actually dedicated to unsupervised exercises. As increasing the duration of MRP has not been associated with improved effectiveness , we postulate that the observed difference relates more to intrinsic advantages of MFRP, such as those described in the previous paragraph. In the present setting, MFRP had a higher direct cost than MRP as there were an increased number of therapeutic interventions administrated over a longer period of time. However, at the societal level, it may be possible that the balance is in favour of MFRP as the rate of return to work was also higher with this programme. Unfortunately a cost analysis was not performed. The clinical characteristics of the sample of patients included in this study make it likely that the results can be transferred to other clinical settings addressing tertiary care of low back pain patients possibly eligible for intensive multidisciplinary functional rehabilitation programmes, but not to other types of settings as such. Additional studies should be performed to discover if the results (in particular the rate of return to work) are maintained over the years.
In conclusion, despite the limitations and in the absence of higher quality evidence on this specific point, we feel that these results provide important information for practitioners and providers alike. MFRP in cLBP patients with severe disability in daily life activities seems to be more effective than a rehabilitation programme based predominantly on muscle reconditioning. Although more demanding for the team, more difficult to set up and with higher direct costs, there are elements (specifically concerning return to work rate) suggesting that these complex interventions could well be cost-effective and thus call for additional studies.
Acknowledgement:We thank all the therapists who participated in these programmes for their dedicated work. We thank Mike Tomcik for his help with the preparation of the manuscript.
Funding / potential competing interests: The study was supported by a grant from Rheuma Search Foundation. The authors declare no conflict of interest.
Correspondence: Anne-Sylvie Steiner, MD, Division of Primary Care Medicine, Department of Community Medicine and Primary Care, University Hospitals of Geneva, Rue Gabrielle-Perret-Gentil 4, CH-1211 Geneva 14, Switzerland, annesylviesteiner[at]hotmail.com
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