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Effects of an exercise and manual therapy program on physical impairments, function and quality-of-life in people with osteoporotic vertebral fracture: a randomised, single-blind controlled pilot trial

BMC Musculoskeletal Disorders volume 11, Article number: 36 (2010) Cite this article

Abstract

Background

This randomised, single-blind controlled pilot trial aimed to determine the effectiveness of a physiotherapy program, including exercise and manual therapy, in reducing impairments and improving physical function and health-related quality of life in people with a history of painful osteoporotic vertebral fracture.

Methods

20 participants were randomly allocated to an intervention (n = 11) or control (n = 9) group. The intervention group attended individual sessions with an experienced clinician once a week for 10 weeks and performed daily home exercises with adherence monitored by a self-report diary. The control group received no treatment. Blinded assessment was conducted at baseline and 11 weeks. Questionnaires assessed self-reported changes in back pain, physical function, and health-related quality of life. Objective measures of thoracic kyphosis, back and shoulder muscle endurance (Timed Loaded Standing Test), and function (Timed Up and Go test) were also taken.

Results

Compared with the control group, the intervention group showed significant reductions in pain during movement (mean difference (95% CI) -1.8 (-3.5 to -0.1)) and at rest (-2.0 (-3.8 to -0.2)) and significantly greater improvements in Qualeffo physical function (-4.8 (-9.2 to -0.5)) and the Timed Loaded Standing test (46.7 (16.1 to 77.3) secs). For the perceived change in back pain over the 10 weeks, 9/11 (82%) participants in the intervention group rated their pain as 'much better' compared with only 1/9 (11%) participants in the control group.

Conclusion

Despite the modest sample size, these results support the benefits of exercise and manual therapy in the clinical management of patients with osteoporotic vertebral fractures, but need to be confirmed in a larger sample.

Trail registration

NCT00638768

Peer Review reports

Background

Vertebral fractures are common sequelae of osteoporosis often resulting in ongoing pain, musculoskeletal, respiratory and postural abnormalities, and deterioration in physical functioning and quality of life [1–5]. Of additional concern, the likelihood of sustaining further fractures increases substantially after an initial fracture [6, 7] and fracture risk is higher in individuals with back muscle weakness and hyper-kyphosis of the thoracic spine [8]. This cyclical relationship between risk of vertebral fracture and physical impairments emphasizes the importance of developing effective treatments to reduce these physical risk factors for subsequent fracture, pain and physical dysfunction.

Currently, drug therapy aimed at improving the underlying osteoporosis is the primary treatment for individuals with vertebral fractures [9]. However, while antiresorptive drugs such as bisphosphonates, hormone therapy, and raloxifenes may address the specific bone deficits, the majority do not directly affect the pain and physical impairments that accompany prevalent vertebral fractures. Physiotherapy is a non-pharmacological treatment that encompasses a range of interventions including manual techniques and exercise and may play an important role in this clinical population through its potential impact on pain, impairment and physical function. However, there are no randomised controlled trials of a multimodal physiotherapy program, and a limited number of studies investigating exercise specifically in people who have sustained a vertebral fracture [10–12].

Therefore, the aim of this pilot study was to evaluate the efficacy of a physiotherapy program which incorporates manual techniques, clinician-led exercises, and home exercises designed to reduce pain, increase back extensor and lower limb muscle strength, and improve posture, trunk stability and trunk mobility. It was hypothesised that improvements in these impairments would result in better physical functioning and quality of life in people with a history of osteoporotic vertebral fracture.

Methods

Design

This study was a single assessor-blinded randomised controlled pilot trial. Potential participants underwent telephone screening and were required to have had a lateral spinal radiograph to diagnose vertebral fracture and dual energy X-ray absorptiometry (DXA) scan of the hip and spine to diagnose osteoporosis based on WHO criteria. Following baseline assessment, eligible participants were randomly allocated to an intervention or control group. The randomisation sequence was generated a priori using the random number function in Excel (Microsoft Corporation, USA) by an independent investigator not directly involved in assessment of participants. These were concealed in opaque envelopes and stored in a locked central location. The envelopes were opened sequentially at the time of intervention assignment by an administrator who informed the treating therapist by facsimilie or email.

Participants

20 men and women (17 F, 3 M) aged over 50 years were recruited from the community via advertisements in local clubs, libraries, and the print and radio media in metropolitan Melbourne, Australia and from medical specialists.

The inclusion criteria were: (i) if female, at least five years post-menopause, defined as a cessation of menstrual cycles for ≥5 years; (ii) aged > 50 years; (iii) primary osteoporosis defined as DXA T score < -2.5 at either the spine or proximal femur with at least one painful vertebral crush or wedge fracture sustained between 3 months and 2 years previously, defined as where the anterior height was reduced by ≥20% compared with its posterior height and the posterior height of the adjacent superior or inferior vertebra [13]; (iv) stable dose of medication for treatment of osteoporosis (eg. hormone replacement therapy, bisphosphonates) for at least 6 months; (v) community dwelling and able to attend for treatment; and (vi) English speaking.

The exclusion criteria were: (i) secondary causes of bone loss such as osteomalacia, glucocorticoid medication; (ii) co-morbidities that would exclude participation in exercise such as severe heart or pulmonary disease, inflammatory joint disease, severe osteoarthritis, psychiatric condition, neuromuscular condition; (iii) acute vertebral fracture sustained within the past 3 months; (iv) radicular signs or symptoms; (v) back pain radiating into the lower limb; (vi) previous participation in a formal pain management program for back pain; (vii) physiotherapy for back pain in the past 6 months; and (viii) allergic reaction to adhesive tape or skin condition that would prevent use of tape.

Ethical approval was obtained from the University of Melbourne Human Research Ethics Committee. All participants provided written informed consent.

Interventions

All participants were requested to refrain from seeking other forms of treatment during the 10 week trial. However, due to ethical considerations, medication was permitted as required.

Intervention group

Participants were treated by one of four experienced physiotherapists located at three private physiotherapy centres for 10 weekly individual sessions each lasting approximately 45 minutes. A number of centres were needed to geographically cover the metropolitan region. The treatment was standardized and the therapists were trained prior to the study to deliver the treatment. A comprehensive treatment manual and DVD were produced for the therapists and the importance of following the protocol emphasised. However, it was considered important to allow the therapists to adjust the intensity of the standardised manual treatment techniques and exercise prescription to match the participants' physical capabilities and change in clinical status: thus the dosage could be altered as required. Deletion of techniques or exercises was permitted if the therapist deemed them inappropriate. At the end of each treatment session for each participant, the physiotherapist completed a checklist to assess adherence with the standard approach.

A standardized progressive treatment protocol was devised based on the literature and clinical experience (Table 1). The aims of the physiotherapy treatment were to i) decrease back pain; ii) improve posture; iii) improve thoracic spine mobility; iv) strengthen trunk extensor and lower limb muscles; v) improve trunk control; vi) provide education. The therapist applied postural taping which was worn full-time for the first week. A protective skin barrier followed by non-rigid, hypoallergenic tape was firstly applied to provide skin protection, followed by rigid strapping tape for postural adjustments and proprioceptive feedback. The taping technique aimed to encourage a retracted scapular and pectoral girdle posture and promote thoracic spine extension. At each treatment session the therapist also performed soft tissue massage and passive accessory central posterior-anterior mobilisation techniques on the thoracic spine. Furthermore, the therapist provided education regarding the aetiology and pathophysiology of osteoporosis, the origin of the pain, the aims of treatment, the importance of patient involvement and adherence, back care, postural awareness and activities to avoid in order to foster positive self management behaviours. The therapist taught the patient exercises to be performed at home: those exercises that addressed posture and range of motion were performed daily whilst strengthening and trunk control exercises were performed three times per week. A 10 week intervention was chosen to allow sufficient time to achieve strength gains in postural muscles and increase spinal mobility [14, 15].

Table 1 Physiotherapy and home exercise program
Full size table

Control group

Control group participants did not receive any additional intervention or complete any home exercises during the 10-week study.

Outcome assessment

Participants were assessed at baseline and at 11 weeks by an assessor blinded to group allocation. Age, gender, number and location of the vertebral fractures, height and body mass were obtained at the baseline assessment.

A number of outcome measures were collected for this study. Overall average back pain in the week prior to assessment was self-assessed at rest and during movement by separate single, 11-point horizontal numeric rating scales with terminal descriptors of (0 = no pain; 10 = worst pain possible). Numeric rating scales have established clinimetric properties in back pain [16] and a change of at least 2 points is thought to represent a clinically meaningful improvement [17, 18]. A similar scale was used to measure average amount of restriction to daily activities in the past week (0 = no restriction; 10 = maximal restriction possible). Participants also rated their perceived change in back pain over the 10 weeks (compared to baseline) on an ordinal scale (1-much worse, 2-slightly worse, 3-no change, 4-slightly better, 5-much better) [18].

Health-related quality of life was measured using one generic questionnaire and one disease-specific questionnaire. The AQoL comprises 15 items on ordinal scales with four levels per item covering five dimensions (illness, independent living, social relationships, physical senses and psychological wellbeing). It produces a single utility index that ranges from -0.04 (worst possible health-related quality of life) to 1.00 (full health-related quality of life). The AQoL has strong psychometric properties [19, 20]. The Qualeffo-41 is a quality-of-life questionnaire especially developed for measuring quality of life in patients with osteoporotic vertebral deformities [20]. It consists of 41 questions arranged in five domains: pain, physical function, social function, general health perception, and mental function. Domain scores plus a total score are scaled from 0 - 100 where a lower score represents better quality of life. The Qualeffo is repeatable and discriminates well between patients with vertebral fractures and control subjects [21].

The Timed Up and Go test is a validated and reliable test of physical function in older individuals [22]. A stop watch was used to time the participant rising from a standard arm chair, walking around a cone on the floor 3 m away, returning to the chair and sitting down again [22]. The participant was barefoot and was asked to perform the task at their own pace. An explanation and demonstration was provided by the investigator but no practice trials were given. The test was performed once.

Thoracic kyphosis was measured using a Dualer Electric Inclinometer (North American Fork, Utah), and followed a previously established protocol [23]. Results of the previous study found high reproducibility (ICC [1,1] = 0.93), (95% CI = 0.66 - 0.99) of this measurement technique, and a standard error of measurement (SEM) of 2° or ± 4.3% of total thoracic kyphosis.

To assess combined trunk and arm endurance in people with vertebral osteoporosis, Shipp et al [24] developed a reliable and valid assessment called the Timed Loaded Standing test. This test measures the time a person can stand while holding a two-pound dumbbell in each hand with the arms at 90 degrees of shoulder flexion and the elbows extended.

Participant adherence was obtained by recording the number of physiotherapy sessions attended (out of a maximum number of 10). Those in the intervention group completed a daily log-book to record the number of home exercise sessions completed. Following the trial completion they were also asked to rate the effort with which they completed the home exercises as well as how frequently they followed the physiotherapist's instructions on five point scales with 1 being 'no effort' or 'never' and 5 being 'maximal effort' or 'always', respectively. Adverse events and the use of co-interventions (including other forms of exercise) were recorded for both groups in a log-book and by open-probe questioning by the assessor at trial completion.

Sample size and data analysis

The primary outcome was average back pain during movement measured on a numeric rating scale. As this was a pilot study, a sample size calculation was not performed. All analyses were conducted on an intention-to-treat principle using all randomized participants using the Statistical Package for the Social Sciences (Norusis/SPSS Inc., Chicago IL, USA). Demographic characteristics, baseline data and adherence data were summarised by descriptive statistics. For outcomes measured using an essentially continuous scale, differences in mean change from baseline were compared between groups using general linear models (analysis of covariance) adjusting for baseline levels of the outcome measure. Measures of participant-perceived change in back pain were presented descriptively. The p value was set at p < 0.05.

Results

We recruited 20 participants (11 physiotherapy, 9 control) and all completed the 10-week trial. Figure 1 shows the flow of participants through the trial. The demographic details of the participants are shown in Table 2. The ages ranged from 53 to 90 years. The majority of participants were women and the three men who took part were all randomised to the intervention group. Seventeen individuals (8 controls, 9 intervention) had a single vertebral level fracture whilst one (control) had fractures at two levels and two (intervention) had fractures at three levels. The majority of fractures occurred in the mid-lower thoracic (T7-T12) region. There were no significant baseline differences between the two groups (Table 2).

Table 2 Demographic information for the physiotherapy and control groups given as the mean (standard deviation) unless otherwise specified
Full size table
Figure 1
figure 1

Flow of participants through trial.

Full size image

There were significant differences in the magnitude of change from baseline in the intervention group compared with the control group for a number of outcome measures (Table 3). The intervention group showed reductions in pain on movement and at rest following the 10 week treatment, while the control group reported increased pain over this time frame. These between-group differences in change in pain were significant. Similarly, the intervention group showed significantly greater improvements in the Qualeffo physical function score compared with the control group. There was no significant difference between groups for changes in other domains of the Qualeffo or in AQoL scores. For the physical impairment measures, there was a significant difference between groups in the Timed Loaded Standing test with the intervention group showing an improvement and the control group deteriorating. There was no difference in change in kyphosis or change in Timed Up and Go scores between groups.

Table 3 Mean (SD) of groups, mean (SD) difference within groups, and mean (95% CI) difference between groups adjusting for the baseline value of the measure, for outcomes with interval data.
Full size table

For the perceived change in back pain over the 10 weeks, 9/11 (82%) participants in the intervention group rated their pain as 'much better' while 1/11 (9%) rated it as 'no change' and 1/11 (9%) rated it as 'much worse'. In contrast, 5/9 (56%) participants in the control group rated their pain as 'no change' with 1/11 (11%) participants rating it in each of the other categories.

Adherence to treatment was excellent. Eight of the 11 participants (73%) in the intervention group attended all 10 treatment sessions with the other three attending four, eight and nine sessions. Home exercise adherence ranged from 34% to 100% with the median (interquartile range) being 95% (78-100%). The home exercises were completed at a median (IQ range) intensity of 4 (3-4) whilst the extent to which the participants followed the physiotherapist's instructions was rated as 5 ('always') by 9/11 (82%) participants.

Six of the intervention group participants (55%) reported adverse events associated with treatment. These were minor and comprised increased shoulder pain (n = 2), flare-up of a wrist injury (n = 1), sore knee (n = 1) and a sore waist (n = 1) with particular exercises as well as irritation with the tape (n = 1). All of these adverse complaints settled after changing or eliminating the aggravating activity. None of the intervention group reported any co-interventions. One participant in the control group received three sessions of physiotherapy due to an increase in back pain. Four control group participants (44%) and four intervention group participants (36%) took medication for pain ranging from 1-14 days in both groups.

Discussion

This single-blind randomised controlled pilot trial found that a 10 week physiotherapy program improved pain, function and physical impairments in people with a history of painful osteoporotic vertebral fracture sustained between 3 months and 2 years previously. To our knowledge, this study is the first RCT to investigate a multimodal physiotherapy program in this patient population. The results support the benefits of combined manual therapy and exercise in the clinical management of patients with osteoporotic vertebral fractures. Moreover, the program was well accepted by participants with 73% attending all physiotherapy sessions and 82% always following instructions from their treating clinician.

Acute pain following a vertebral fracture often settles within a few weeks although many individuals experience chronic pain with the risk of pain generally increasing with the number and severity of vertebral fractures [25]. In fact, a recent case series of 107 consecutive patients found that 80% still had pronounced pain one year after the fracture [26]. In our study, pain during movement and at rest was reduced by 42% and 63% respectively in the intervention group whilst the control group showed increases in pain of 48% and 43%. The difference in change in rest pain between groups was of an amount that is considered clinically meaningful (2 points) while the difference in change in movement pain between groups approached this clinically meaningful amount [17]. The benefits were also confirmed by the results from the Qualeffo pain subscale and by the participants' overall rating of change in back pain. No major adverse events were reported by participants in the intervention group, suggesting that the manual therapy and exercise interventions were safe.

Lower quality of life has also been reported in individuals with vertebral fracture [27] and the mean (SD) AQoL score for our sample of 0.53 (0.20) is much lower than the comparable Australian population mean for 60-69 year olds of 0.79 (0.19) [28]. Despite reduced health-related quality of life in our sample, there was no significant improvement following the intervention as measured by the total Qualeffo score or the AQoL although trends were noted. Significant benefits were seen in the physical function domain of the Qualeffo which is not surprising given that the treatment focused on techniques to address physical impairments. Psychological interventions such as cognitive behavioural therapy may be needed to reduce psychological impairments that impact on quality of life such as anxiety, fear and depression, consistent with the biopsychosocial model of treating chronic musculoskeletal pain.

The intervention aimed to reduce thoracic kyphosis because of the relationship between the magnitude of kyphosis and spinal loads [29]. Patients with vertebral fracture have been found to have a greater kyphosis than their age-matched counterparts [30–32] and higher spinal loads as a consequence [33]. This may contribute to the well-documented increased risk of subsequent fractures after an individual has sustained an initial vertebral fracture. In addition to the mechanical loading implications of thoracic kyphosis, functional implications include limitations in pulmonary function, compromised balance and therefore increased falls risk, and exacerbation of back extensor muscle weakness [32]. These highlight a biomechanical rationale for treatment modalities aimed at reducing kyphosis.

While it is recognised that there will be a degree of fixed structural thoracic kyphosis [34], often times the kyphosis is compounded by habitually-poor posture and weakness of the back extensor muscles. Given a potentially-modifiable component to the kyphosis, our intervention program incorporated postural retraining, and exercises to improve range of thoracic extension and strength of the back extensor and posterior shoulder musculature. Postural taping was worn full-time for the first week to provide patients with the sensation of improved posture to facilitate postural retraining. In another study we found that postural tape led to an immediate 5% reduction in thoracic kyphosis in 15 patients with vertebral fracture [23]. Given that there were no associated changes in the surface electromyographic activity of the trunk muscles, the reduction in kyphosis was likely to have been achieved passively through mechanical support from the tape and activation of deep postural muscles. In the current study, a similar reduction (5%) in thoracic kyphosis was found following treatment in the intervention group compared to no change in the control group. This difference was larger than the standard error of measurement of ± 2 degrees or ± 4.3% [23] but the result did not reach statistical significance probably due to the small sample size. It is also possible that a longer time frame is needed to yield larger effects: one case series showed that an orthotic brace worn over 6 months led to an 11% reduction in kyphosis [35].

Our strengthening exercises concentrated specifically on the back extensor and posterior trunk postural muscles in order to promote a more neutral spinal posture and minimise deleterious flexion moments [29, 33]. The exercises were of low intensity in order to minimise compression loads through already-weakened vertebrae and to target slow twitch muscle fibres which predominate these muscle groups [36]. We did not use a maximum strength test for the back extensor muscles because of the potential risk of further vertebral fracture. Instead we used the Timed Loaded Standing test to indicate combined trunk and arm muscle endurance [24]. The intervention group showed a 65% improvement in holding time whilst the control group showed a 26% reduction. This suggests that the intervention was effective in increasing muscle endurance although part of the improvement may also be related to a reduction in back pain. Similarly, performance of a single low-intensity back extensor exercise in a group of postmenopausal women with osteoporosis, some of whom had vertebral fractures, significantly improved back extensor strength as well as quality-of-life over a 4 month period [37]. We have also found altered neuromuscular patterns of paraspinal muscle activity in individuals who have sustained vertebral fractures compared to those without fracture [38]. This suggests that in addition to strengthening, specific neuromuscular retraining might be effective.

Our program included manual therapy that involved mobilising techniques applied gently to the thoracic spine. Application of central postero-anterior force (Maitland-mobilisation) to thoracic spinous processes causes extension of the thoracic motion segments [39], leading to improved range of movement into extension locally and at adjacent motion segments [40, 41]. Ultimately, manual therapy of this nature may improve active extension range and reduce pain related to intervertebral stiffness. Whilst a survey of Canadian physiotherapists revealed that manual therapy is used by 45% of therapists in the management of patients with osteoporosis, over 91% had concerns about its safety particularly with regards to causing vertebral or rib fractures [42]. However, a study designed to investigate the safety of spinal mobilization showed that the in vivo loads applied by therapists during these techniques were well below in vitro fracture loads, suggesting a reasonable safety margin [39]. We also had no adverse effects related to the manual therapy components of our program.

Given that our intervention was multimodal, it is not possible to establish which of the individual treatment components was more or less effective or which contributed to each of the outcomes observed. It is also possible that a mechanism underlying part of the improvements in the physiotherapy group relates to the therapeutic environment including interaction with the therapist rather than the interventions per se. Given that our control group received no treatment rather than placebo physiotherapy, this cannot be ascertained. However, the placebo effect has been found to be apparent for pain but less so for other physical measurements [43]. Thus, the improvements noted for the other measurements such as the Timed Loaded Standing test are more likely to be due to the specific techniques and exercises.

There are few randomised controlled trials investigating the effectiveness of conservative, non-pharmacological interventions applied in the chronic phase to the osteoporotic population with vertebral fractures. Malmros et al [11] found that a 10-week exercise program that focused on balance, strength and lumbar stabilisation improved balance and level of daily function and decreased pain and use of analgesics. This study also demonstrated improvement in the quality of life of participants even beyond the active training period. Another study investigating a 6-month minimally-supervised home-based exercise program comprising stretching, strengthening and walking also improved quality of life with benefits sustained at 12 months [12]. Gold et al [10] found that in 185 older women (mean age of 81 years), group exercise and coping classes for six months delivered by a physiotherapist and social worker led to improvements in back extensor strength and psychological impairments but not in pain levels. That pain was not reduced may relate to the fact that only 40% of the participants reported pain in the previous month. Our results offer preliminary evidence for the efficacy of rehabilitative interventions delivered after a symptomatic osteoporotic vertebral fracture. The efficacy of these interventions for reducing the risk of incident fracture should now be explored.

Our study has several limitations. First, the most obvious is the small sample size. However despite this, significant differences in outcomes were found between the intervention and control groups. These results need to be confirmed in a larger sample. Furthermore we did not adjust the analyses for multiple comparisons which increases the risk of making a Type 1 error. Nevertheless, the results were consistent across several measurement instruments. Second is that neither the participants nor the care providers were blinded which may exaggerate the estimates of treatment effects [44]. However, there is some debate in the literature about whether it is appropriate to use a placebo treatment for interventions such as physiotherapy where it is difficult to isolate the direct and indirect effects of the therapy [45]. It has been argued that these effects are unlikely to be distinct, additive and divisible and that using a placebo-controlled trial design will not detect the whole treatment effect and may in fact generate false negative results. Third, as we did not include a follow up assessment, compliance with unsupervised home exercises and maintenance of benefits over time are unknown. Fourth, whether our physiotherapy program reduces the risk of future fracture would need to be tested in a larger cohort over a longer period. Such a benefit was noted in a prospective 10 year follow up study where a back extensor strengthening program was effective in reducing the risk of subsequent vertebral fracture in post menopausal women [46]. Fifth, as participants were unable to consistently identify a mechanism of injury for their vertebral fracture(s), consistent with the stochastic nature of vertebral fractures [47], we are unable to judge the efficacy of the intervention program relative to the fracture mechanism. Finally, the majority of fractures in our sample were located in the thoracic region. Given evidence that lumbar fractures are associated with more severe pain and lower quality-of-life than thoracic fractures [48, 49], the results may not be directly generalisable to lumbar fractures.

Conclusions

This randomised controlled trial found that a 10-week program of physiotherapy was effective in reducing pain and improving physical function and back muscle endurance in a group of 19 individuals with a history of painful vertebral fracture. Despite the modest sample size, these results support the benefits of exercise and manual therapy in the clinical management of patients with osteoporotic vertebral fractures, but need to be confirmed in a larger sample.

References

  1. Hallberg I, Rosenqvist AM, Kartous L, Lofman O, Wahlstrom O, Toss G: Health-related quality of life after osteoporotic fractures. Osteoporos Int. 2004, 15 (10): 834-841. 10.1007/s00198-004-1622-5.

    Article  CAS  PubMed  Google Scholar 

  2. Lyles KW, Gold DT, Shipp KM, Pieper CF, Martinez S, Mulhausen PL: Association of osteoporotic vertebral compression fractures with impaired functional status. Am J Med. 1993, 94 (6): 595-601. 10.1016/0002-9343(93)90210-G.

    Article  CAS  PubMed  Google Scholar 

  3. Pluijm SM, Tromp AM, Smit JH, Deeg DJ, Lips P: Consequences of vertebral deformities in older men and women. J Bone Miner Res. 2000, 15 (8): 1564-1572. 10.1359/jbmr.2000.15.8.1564.

    Article  CAS  PubMed  Google Scholar 

  4. Scane AC, Francis RM, Sutcliffe AM, Francis MJ, Rawlings DJ, Chapple CL: Case-control study of the pathogenesis and sequelae of symptomatic vertebral fractures in men. Osteoporos Int. 1999, 9 (1): 91-97. 10.1007/s001980050120.

    Article  CAS  PubMed  Google Scholar 

  5. Silverman SL, Piziak VK, Chen P, Misurski DA, Wagman RB: Relationship of health related quality of life to prevalent and new or worsening back pain in postmenopausal women with osteoporosis. J Rheumatol. 2005, 32 (12): 2405-2409.

    PubMed  Google Scholar 

  6. Lindsay R, Silverman SL, Cooper C, Hanley DA, Barton I, Broy SB, Licata A, Benhamou L, Geusens P, Flowers K, et al.: Risk of new vertebral fracture in the year following a fracture. Jama. 2001, 285 (3): 320-323. 10.1001/jama.285.3.320.

    Article  CAS  PubMed  Google Scholar 

  7. Lunt M, O'Neill TW, Felsenberg D, Reeve J, Kanis JA, Cooper C, Silman AJ: Characteristics of a prevalent vertebral deformity predict subsequent vertebral fracture: results from the European Prospective Osteoporosis Study (EPOS). Bone. 2003, 33 (4): 505-513. 10.1016/S8756-3282(03)00248-5.

    Article  PubMed  Google Scholar 

  8. Huang MH, Barrett-Connor E, Greendale GA, Kado DM: Hyperkyphotic posture and risk of future osteoporotic fractures: the Rancho Bernardo study. J Bone Miner Res. 2006, 21 (3): 419-423. 10.1359/JBMR.051201.

    Article  PubMed  Google Scholar 

  9. Francis RM, Aspray TJ, Hide G, Sutcliffe AM, Wilkinson P: Back pain in osteoporotic vertebral fractures. Osteoporos Int. 2008, 19 (7): 895-903. 10.1007/s00198-007-0530-x.

    Article  CAS  PubMed  Google Scholar 

  10. Gold DT, Shipp KM, Pieper CF, Duncan PW, Martinez S, Lyles KW: Group treatment improves trunk strength and psychological status in older women with vertebral fractures: results of a randomized, clinical trial. J Am Geriatr Soc. 2004, 52 (9): 1471-1478. 10.1111/j.1532-5415.2004.52409.x.

    Article  PubMed  Google Scholar 

  11. Malmros B, Mortensen L, Jensen MB, Charles P: Positive effects of physiotherapy on chronic pain and performance in osteoporosis. Osteoporos Int. 1998, 8 (3): 215-221. 10.1007/s001980050057.

    Article  CAS  PubMed  Google Scholar 

  12. Papaioannou A, Adachi JD, Winegard K, Ferko N, Parkinson W, Cook RJ, Webber C, McCartney N: Efficacy of home-based exercise for improving quality of life among elderly women with symptomatic osteoporosis-related vertebral fractures. Osteoporos Int. 2003, 14 (8): 677-682. 10.1007/s00198-003-1423-2.

    Article  CAS  PubMed  Google Scholar 

  13. McCloskey EV, Spector TD, Eyres KS, Fern ED, O'Rourke N, Vasikaran S, Kanis JA: The assessment of vertebral deformity: a method for use in population studies and clinical trials. Osteoporos Int. 1993, 3 (3): 138-147. 10.1007/BF01623275.

    Article  CAS  PubMed  Google Scholar 

  14. Benedetti MG, Berti L, Presti C, Frizziero A, Giannini S: Effects of an adapted physical activity program in a group of elderly subjects with flexed posture: clinical and instrumental assessment. J Neuroeng Rehabil. 2008, 25: 32-10.1186/1743-0003-5-32.

    Article  Google Scholar 

  15. Danneels LA, Cools AM, Vanderstraeten GG, Cambier DC, Witvrouw EE, Bourgois J, de Cuyper HJ: The effects of three different training modalities on the cross-sectional area of the paravertebral muscles. Scand J Med Sci Sports. 2001, 11: 335-41. 10.1034/j.1600-0838.2001.110604.x.

    Article  CAS  PubMed  Google Scholar 

  16. Jensen MP, Turner JA, Romano JM, Fisher LD: Comparative reliability and validity of chronic pain intensity measures. Pain. 1999, 83 (2): 157-162. 10.1016/S0304-3959(99)00101-3.

    Article  CAS  PubMed  Google Scholar 

  17. Childs JD, Piva SR, Fritz JM: Responsiveness of the numeric pain rating scale in patients with low back pain. Spine. 2005, 30 (11): 1331-1334. 10.1097/01.brs.0000164099.92112.29.

    Article  PubMed  Google Scholar 

  18. Ostelo RW, de Vet HC: Clinically important outcomes in low back pain. Best Pract Res Clin Rheumatol. 2005, 19 (4): 593-607. 10.1016/j.berh.2005.03.003.

    Article  PubMed  Google Scholar 

  19. Osborne RH, Hawthorne G, Lew EA, Gray LC: Quality of life assessment in the community-dwelling elderly: validation of the Assessment of Quality of Life (AQoL) Instrument and comparison with the SF-36. J Clin Epidemiol. 2003, 56 (2): 138-147. 10.1016/S0895-4356(02)00601-7.

    Article  PubMed  Google Scholar 

  20. Whitfield K, Buchbinder R, Segal L, Osborne RH: Parsimonious and efficient assessment of health-related quality of life in osteoarthritis research: validation of the Assessment of Quality of Life (AQoL) instrument. Health Qual Life Outcomes. 2006, 4: 19-10.1186/1477-7525-4-19.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Lips P, Cooper C, Agnusdei D, Caulin F, Egger P, Johnell O, Kanis JA, Kellingray S, Leplege A, Liberman UA, et al.: Quality of life in patients with vertebral fractures: validation of the Quality of Life Questionnaire of the European Foundation for Osteoporosis (QUALEFFO). Working Party for Quality of Life of the European Foundation for Osteoporosis. Osteoporos Int. 1999, 10 (2): 150-160. 10.1007/s001980050210.

    Article  CAS  PubMed  Google Scholar 

  22. Podsiadlo D, Richardson S: The timed "Up & Go": a test of basic functional mobility for frail elderly persons. J Am Geriatr Soc. 1991, 39 (2): 142-148.

    Article  CAS  PubMed  Google Scholar 

  23. Greig AM, Bennell KL, Briggs AM, Hodges PW: Postural taping decreases thoracic kyphosis but does not influence trunk muscle electromyographic activity or balance in women with osteoporosis. Man Ther. 2008, 13 (3): 249-257. 10.1016/j.math.2007.01.011.

    Article  PubMed  Google Scholar 

  24. Shipp KM, Purse JL, Gold DT, Pieper CF, Sloane R, Schenkman M, Lyles KW: Timed loaded standing: a measure of combined trunk and arm endurance suitable for people with vertebral osteoporosis. Osteoporos Int. 2000, 11 (11): 914-922. 10.1007/s001980070029.

    Article  CAS  PubMed  Google Scholar 

  25. Suzuki N, Ogikubo O, Hansson T: The course of the acute vertebral body fragility fracture: its effect on pain, disability and quality of life during 12 months. Eur Spine J. 2008, 17 (10): 1380-1390. 10.1007/s00586-008-0753-3.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Suzuki N, Ogikubo O, Hansson T: The prognosis for pain, disability, activities of daily living and quality of life after an acute osteoporotic vertebral body fracture: its relation to fracture level, type of fracture and grade of fracture deformation. Eur Spine J. 2008, 18 (1): 77-88. 10.1007/s00586-008-0847-y.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Borgstrom F, Zethraeus N, Johnell O, Lidgren L, Ponzer S, Svensson O, Abdon P, Ornstein E, Lunsjo K, Thorngren KG: Costs and quality of life associated with osteoporosis-related fractures in Sweden. Osteoporos Int. 2006, 17 (5): 637-650. 10.1007/s00198-005-0015-8.

    Article  PubMed  Google Scholar 

  28. Hawthorne G, Osborne R: Population norms and meaningful differences for the Assessment of Quality of Life (AQoL) measure. Aust N Z J Public Health. 2005, 29 (2): 136-142. 10.1111/j.1467-842X.2005.tb00063.x.

    Article  PubMed  Google Scholar 

  29. Briggs AM, van Dieen JH, Wrigley TV, Greig AM, Phillips B, Lo SK, Bennell KL: Thoracic kyphosis affects spinal loads and trunk muscle force. Phys Ther. 2007, 87 (5): 595-607.

    Article  PubMed  Google Scholar 

  30. Cortet B, Roches E, Logier R, Houvenagel E, Gaydier-Souquieres G, Puisieux F, Delcambre B: Evaluation of spinal curvatures after a recent osteoporotic vertebral fracture. Joint Bone Spine. 2002, 69 (2): 201-208. 10.1016/S1297-319X(02)00381-0.

    Article  PubMed  Google Scholar 

  31. Keller TS, Harrison DE, Colloca CJ, Harrison DD, Janik TJ: Prediction of osteoporotic spinal deformity. Spine. 2003, 28 (5): 455-462. 10.1097/00007632-200303010-00009.

    PubMed  Google Scholar 

  32. Lombardi I, Oliveira LM, Mayer AF, Jardim JR, Natour J: Evaluation of pulmonary function and quality of life in women with osteoporosis. Osteoporos Int. 2005, 16 (10): 1247-1253. 10.1007/s00198-005-1834-3.

    Article  PubMed  Google Scholar 

  33. Briggs AM, Wrigley TV, van Dieen JH, Phillips B, Lo SK, Greig AM, Bennell KL: The effect of osteoporotic vertebral fracture on predicted spinal loads in vivo. Eur Spine J. 2006, 15 (12): 1785-1795. 10.1007/s00586-006-0158-0.

    Article  PubMed  Google Scholar 

  34. Goh S, Price RI, Leedman PJ, Singer KP: The relative influence of vertebral body and intervertebral disc shape on thoracic kyphosis. Clin Biomech (Bristol, Avon). 1999, 14 (7): 439-448. 10.1016/S0268-0033(98)00105-3.

    Article  CAS  Google Scholar 

  35. Pfeifer M, Begerow B, Minne HW: Effects of a new spinal orthosis on posture, trunk strength, and quality of life in women with postmenopausal osteoporosis: a randomized trial. Am J Phys Med Rehabil. 2004, 83 (3): 177-186. 10.1097/01.PHM.0000113403.16617.93.

    Article  PubMed  Google Scholar 

  36. Mannion AF, Dumas GA, Cooper RG, Espinosa FJ, Faris MW, Stevenson JM: Muscle fibre size and type distribution in thoracic and lumbar regions of erector spinae in healthy subjects without low back pain: normal values and sex differences. J Anat. 1997, 190 (Pt 4): 505-513. 10.1046/j.1469-7580.1997.19040505.x.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Hongo M, Itoi E, Sinaki M, Miyakoshi N, Shimada Y, Maekawa S, Okada K, Mizutani Y: Effect of low-intensity back exercise on quality of life and back extensor strength in patients with osteoporosis: a randomized controlled trial. Osteoporos Int. 2007, 18 (10): 1389-1395. 10.1007/s00198-007-0398-9.

    Article  CAS  PubMed  Google Scholar 

  38. Briggs AM, Greig AM, Bennell KL, Hodges PW: Paraspinal muscle control in people with osteoporotic vertebral fracture. Eur Spine J. 2007, 16 (8): 1137-1144. 10.1007/s00586-006-0276-8.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Sran MM, Khan KM, Zhu Q, McKay HA, Oxland TR: Failure characteristics of the thoracic spine with a posteroanterior load: investigating the safety of spinal mobilization. Spine. 2004, 29 (21): 2382-2388. 10.1097/01.brs.0000143110.59837.f2.

    Article  PubMed  Google Scholar 

  40. Powers CM, Kulig K, Harrison J, Bergman G: Segmental mobility of the lumbar spine during a posterior to anterior mobilization: assessment using dynamic MRI. Clin Biomech (Bristol, Avon). 2003, 18 (1): 80-83. 10.1016/S0268-0033(02)00174-2.

    Article  Google Scholar 

  41. Twomey LT: A rationale for the treatment of back pain and joint pain by manual therapy. Phys Ther. 1992, 72 (12): 885-892.

    CAS  PubMed  Google Scholar 

  42. Sran MM, Khan KM: Physiotherapy and osteoporosis: practice behaviors and clinicians' perceptions--a survey. Man Ther. 2005, 10 (1): 21-27. 10.1016/j.math.2004.06.003.

    Article  PubMed  Google Scholar 

  43. Hrobjartsson A, Gotzsche PC: Is the placebo powerless? An analysis of clinical trials comparing placebo with no treatment. N Engl J Med. 2001, 344 (21): 1594-1602. 10.1056/NEJM200105243442106.

    Article  CAS  PubMed  Google Scholar 

  44. Schulz KF, Chalmers I, Hayes RJ, Altman DG: Empirical evidence of bias. Dimensions of methodological quality associated with estimates of treatment effects in controlled trials. Jama. 1995, 273 (5): 408-412. 10.1001/jama.273.5.408.

    Article  CAS  PubMed  Google Scholar 

  45. Paterson C, Dieppe P: Characteristic and incidental (placebo) effects in complex interventions such as acupuncture. Bmj. 2005, 330 (7501): 1202-1205. 10.1136/bmj.330.7501.1202.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Sinaki M, Itoi E, Wahner HW, Wollan P, Gelzcer R, Mullan BP, Collins DA, Hodgson SF: Stronger back muscles reduce the incidence of vertebral fractures: a prospective 10 year follow-up of postmenopausal women. Bone. 2002, 30 (6): 836-841. 10.1016/S8756-3282(02)00739-1.

    Article  CAS  PubMed  Google Scholar 

  47. Briggs AM, Greig AM, Wark JD: The vertebral fracture cascade in osteoporosis: a review of aetiopathogenesis. Osteoporos Int. 2007, 18 (5): 575-584. 10.1007/s00198-006-0304-x.

    Article  CAS  PubMed  Google Scholar 

  48. Cockerill W, Ismail AA, Cooper C, Matthis C, Raspe H, Silman AJ, O'Neill TW: Does location of vertebral deformity within the spine influence back pain and disability? European Vertebral Osteoporosis Study (EVOS) Group. Ann Rheum Dis. 2000, 59 (5): 368-371. 10.1136/ard.59.5.368.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Oleksik A, Lips P, Dawson A, Minshall ME, Shen W, Cooper C, Kanis J: Health-related quality of life in postmenopausal women with low BMD with or without prevalent vertebral fractures. J Bone Miner Res. 2000, 15 (7): 1384-1392. 10.1359/jbmr.2000.15.7.1384.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

This trial was funded by a grant from the ANZ Charitable Trusts. We wish to acknowledge the project physiotherapists Jodi Hendler, Greg Gibson and Libby Oldfield.

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Authors and Affiliations

  1. Centre for Health, Exercise & Sports Medicine, Melbourne Physiotherapy School, University of Melbourne, Australia

    Kim L Bennell, Bernadette Matthews, Anne Kelly & Margaret Sherburn

  2. Department of Physical Therapy, University of British Columbia, Canada

    Alison Greig

  3. School of Physiotherapy and Curtin Health Innovation Research Institute, Curtin University of Technology, Australia

    Andrew Briggs

  4. Hydrotherapy Consulting and Training, Brisbane, Australia

    Judy Larsen

  5. University of Melbourne Department of Medicine and Bone & Mineral Service, Royal Melbourne Hospital, Australia

    John Wark

Authors
  1. Kim L Bennell
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  2. Bernadette Matthews
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  6. Margaret Sherburn
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Correspondence to Kim L Bennell.

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The authors declare that they have no competing interests.

Authors' contributions

All authors read and approved the final manuscript. KB conceived of the study and participated in its design. She was the overall co-ordinator of the study and developed the physiotherapy treatment, trained the therapists, performed the statistical analyses and wrote the first draft of the paper. BM assisted with recruitment, training of physiotherapists and performed the outcome assessments. AG assisted with recruitment, testing and contributed to the writing of the manuscript. AB assisted with recruitment and contributed to the writing of the manuscript. AK assisted with recruitment and co-ordination of the study. MS was involved with the design of the study, developed the physiotherapy treatment and assisted with training of therapists. JL was involved with the design of study and development of the treatment protocol. JW was involved with the design of the study and drafting the manuscript. All authors read and approve the final paper.

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Bennell, K.L., Matthews, B., Greig, A. et al. Effects of an exercise and manual therapy program on physical impairments, function and quality-of-life in people with osteoporotic vertebral fracture: a randomised, single-blind controlled pilot trial. BMC Musculoskelet Disord 11, 36 (2010). https://0-doi-org.brum.beds.ac.uk/10.1186/1471-2474-11-36

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Keywords

BMC Musculoskeletal Disorders

ISSN: 1471-2474

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