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<p>Neurodynamics refers to the mechanical and physiological components of</p> <p>the nervous system and the interconnections between them (Shacklock, 1995).</p> <p>This is a phase 1 pilot trial investigating the immediate effect of a neurodynamic</p> <p>treatment as compared to a sham treatment in eight participants with low back</p> <p>pain. Primary outcome measures included: H-reflex latency and nerve</p> <p>conduction velocity. Secondary outcome measures included: the sitting slump</p> <p>test and visual analog scale for pain following a neurodynamic treatment</p> <p>compared to a sham treatment on eight participants with low back pain. T-tests</p> <p>were used to analyze any differences between the groups at baseline and post-</p> <p>intervention. No statistically significant differences were observed between the</p> <p>groups at baseline. Statistically significant differences were noted post-</p> <p>intervention between the treatment groups for H-reflex latency (t(5)=4.323,</p> <p>p=0.008) and the unaffected leg sitting slump test (t(5)=3.402, p=0.019). The H-</p> <p>reflex latency increased for the group following the neurodynamic treatment and</p> <p>decreased following the sham treatment. This was not expected and is of</p> <p>interest due to the possible mechanisms that may be underlying these</p> <p>phenomena. Despite the small sample size used in this study, differences were</p> <p>observed and displayed trends that were unanticipated. These between-group</p> <p>differences are of interest but require further investigation using a larger sample</p> <p>population. Sample size calculations for future studies based on the primary</p> <p>outcome measures yielded a sample of 2008 participants. This accounted for</p> <p>both a 20% difference between the two groups and a 20% dropout rate. Future</p> <p>studies need to investigate the most beneficial length of time, type and dosage of</p> <p>neurodynamic treatments, as well as, the most appropriate times to assess the</p> <p>outcome measures. Comparison to controls would be beneficial in subsequent</p> <p>studies.</p> / Master of Science Rehabilitation Science (MSc)

Low back pain is a common medical problem around the world afflicting 80% of the population some time in their life. Low back injury can result from a loss of torso stability causing excessive strain in soft tissue. This investigation seeks to apply existing methods to new applications and to develop new methods to assess torso stability. First, the time series averaged finite time Lyapunov exponent is calculated from data obtained during seated stability experiments. The Lyapunov exponent is found to increase with increasing task difficulty. Second, a new metric for evaluating torso stability is introduced, the threshold of stability. This parameter is defined as the maximum task difficulty in which dynamic stability can be maintained for the test duration. The threshold of stability effectively differentiates torso stability at two levels of visual feedback. Third, the state space distribution of the finite time Lyapunov exponent (FTLE) field is evaluated for deterministic and stochastic systems. Two new methods are developed to generate the FTLE field from time series data. Using these methods, Lagrangian coherent structures (LCS) are found for an inverted pendulum, the Acrobot, and planar wobble chair models. The LCS are ridges in the FTLE field that separate two inherently different types of motion when applied to rigid-body dynamic systems. As a result, LCS can be used to identify the boundaries of the basin of stability. Finally, these new methods are used to find the basin of stability from time series data collected from torso stability experiments. The LCS and basins of stability provide a richer understanding into the system dynamics when compared to existing methods. By gaining a better understanding of torso stability, it is hoped this knowledge can be used to prevent low back injury and pain in the future. These new methods may also be useful in evaluating other biodynamic systems such as standing postural sway, knee stability, or hip stability as well as time series applications outside the area of biomechanics. / Ph. D.

The goal of this research study was to create an artificial annulus fibrosus similar to that of the natural intervertebral disc, as well as find preliminary results for vertebral endplate connection and nucleus pulposus internal pressure, for the correction of disc degeneration in the spine. The three-part composite samples needed to demonstrate good shock absorption and load distribution while maintaining strength and flexibility, and removing the need for metal in the body, something of which no current total disc replacement or spinal fusion surgery can offer. For this study, the spinal disc was separated into its three different components, the annulus fibrosus, the nucleus pulposus, and the vertebral endplates, each playing a vital role in the function of the disc. Two low-cost materials were selected, a Covestro polyurethane and cellulose nanocrystals, for the purpose of creating a polymer composite spinal disc implant. A methodology was established for creating the cast composite material for use as an annulus fibrosus, while also investigating its mechanical properties. The same composite material was used to acquire preliminary results for vertebral endplate connection to the synthesized annulus, however no additional material was used to determine or mimic the mechanical properties of these endplates, due to time constraints. Also because of time constraints, the nucleus used in this study was only comprised of water with no other additives for preliminary testing since the natural nucleus is comprised of about 80-90% water. These properties were then compared to the mechanical properties of the natural disc, so that they could be finely tuned to emulate the natural disc. It is shown in this study that the composite material, when swelled in water, was able to mimic the annulus fibrosus in tensile strength and modulus, however showed higher compressive strength and modulus than ideal. The samples also did not undergo any permanent deformation within the realm of force actually introduced to the natural disc. The vertebral endplates showed decent adhesion to the synthesized annulus, however there were slight defects that became failure concentrators during compression testing. The nucleus showed promising results maintaining good internal pressure to the system causing better compressive load distribution, with barreling of the samples. / Master of Science / Spinal disc degeneration is a very prevalent problem in today’s society, effecting anywhere from 12% to 35% of a given population. It usually occurs in the lumbar section of the spine, and when severe enough, can cause bulging and herniation of the intervertebral disc itself. This can cause immense lower back pain in individual’s stricken with this disease, and in the US, medical costs associated with lower back pain to exceed $100 billion. Current solutions to this problem include multiple different treatment options of which, spinal fusion surgery and total disc replacement (TDR) are among the most common. Although these treatments cause pain relief for the majority of patients, there are multiple challenges that come with these options. For example, spinal fusion surgery severely limits the mobility of its patients by fusing two vertebrae together, disallowing any individual movement, and TDR can cause hypermobility in among the vertebrae and offer little to no shock absorption of loads. Therefore, a better treatment option is needed to relieve the pain of the patients, as well as maintain equal motion, shock absorption, and load cushioning to that of the normal intervertebral disc and remaining biocompatible. The goal of this research study was to create a three-component system, like that of the natural intervertebral disc, for the use of spinal disc replacement and to replace current options. The fabricated system was comprised of the three components found in the natural intervertebral disc; the annulus fibrosus, the nucleus pulposus, and the vertebral endplates. Because the system will need to go in-body, the materials used were all characterized as biocompatible materials; the polyurethane currently being used in medical devices and implants, and the cellulose nanocrystals (CNCs) coming from natural cellulose in sources such as wood and plants. The results determined that the mechanical properties of the system can be fine-tuned in order to mimic the natural strength and cushioning capabilities of the natural disc, based on CNC content added to the polyurethane, and when all three components of the system are added together, the compressive stress-strain is most similar to the natural disc in compression. However, the system did show failure in the connection between the annulus fibrosus and vertebral endplates, causing herniation of the nucleus similar to the initial problem attempting to be solved. For this, more ideal fabrication methods should be researched in the future including 3D printing techniques, injection molding, and roll milling. As well as alternate fabrication techniques, cell grow and viability should be determined to show that cells don’t die once the system in implanted.

Yes / The project was designed as a retrospective service evaluation using audit to assess the identification and documentation of red flags in initial assessment of patients with low back pain. Firstly, the documentation of 11 predetermined red flags was assessed. Secondly, the documentation of relevant additional information was assessed and finally, compliance with local policy to highlight positive red flag findings in the designated area on the paperwork was examined. The documentation for the majority of red flags was high, however, clear gaps were identified. Additionally, there was no evidence of further clinical consideration of positive red flags during the diagnostic process. Possible factors influencing red flag documentation are discussed and suggestions are provided to improve recording and response to clinical indicators of malignancy.

Background: Rowing is a demanding sport where extreme positions and high physical loads are obtained. This leads to injury risks, especially in the lower back. Another issue relates to comfortability. When rowing, the buttocks are the pivot point, and lots of pressure is placed on the sitting bones and surrounding tissues. For para-rowers, these issues can be even more prominent and important to consider. Purpose and aim: The purpose of this project was to develop a solution that enhances the enjoyment and comfortability for para-rowers. To do that, this project aimed to develop an individualized add-on product for rowing seats, with an included method to translate individual measurements into the design. Method: The Double Diamond Model was used to guide the project, where both qualitative and quantitative methods were included to reach the aim and purpose. To discover and define the problem, data was collected with literature review, benchmarking, and semi-structured interviews. With that data as a base, concepts were developed and selected, and the selected concept was tested with regards to pressure distribution. Results: The final concept was based on one individual and includes a seating area that has the exact shape of that individual. It does also include an increased back support and sideways support. To get measurements to design the individualized seat, a method consisting of scanning a vacuum pillow was used. Conclusion: The findings indicate that a perfectly fitted seat will spread out pressure more evenly around the buttocks, which enhances comfortability. There is, though, still much to consider and evaluate before this product can reach the market.

Thesis (MScPhysio)--Stellenbosch University, 2015. / ENGLISH ABSTRACT: Aims: To assess the effect of a chair and computer screen height adjustment on the neck and upper back musculoskeletal symptoms in an office worker. Methods: An N=1 study was conducted using the ABC design. Ethics approval was obtained for the study and the participant provided informed written consent. The participant was assessed over three four week phases as she performed her habitual computer work. The outcome measures assessed during the three phases were the pain intensity and perceived sitting comfort. The three phases were named the baseline, intervention and wash-out phases. During the baseline phase, the outcome measures were obtained at the participant‟s habitual work station. The intervention phase involved a vertical adjustment of the chair and computer screen height. The wash-out phase allowed the participant to adjust the chair and computer screen height to their choice. A follow-up interview was conducted with the participant three months after completion of the study. The mean values and the ranges of the pain intensity and perceived comfort were obtained and compared. The data collected was captured on a Microsoft Excel 2010 spread sheet, where after the data was tabulated and presented graphically. Results: The mean pain intensity of the participant increased slightly during the intervention phase in comparison to the baseline phase, but remained stable during the wash-out phase. The mean perceived sitting comfort deteriorated initially during the intervention phase, but improved later during the intervention phase and showed greater improvement during the wash out phase. The perceived sitting comfort showed more improvement than the pain intensity during the washout phase. Both the pain intensity and perceived sitting comfort showed improvement at the three months follow up assessment, post completion of the study. Conclusion: The vertical height adjustment of the chair and the VDT did not improve the participant‟s pain intensity and perceived sitting comfort when compared to the participant‟s habitual workstation parameters. The findings do not favour the horizontal viewing angle. The findings of this study however support the use of „slightly below horizontal‟ viewing angle as being conducive to reduce the pain intensity and improve the sitting comfort of an office worker. / AFRIKAANSE OPSOMMING: Doelstelling: Om die effek te bepaal van die hoogte aanpassing van die stoel en rekenaarskerm op die nek en bo-rug muskuloskeletale simptome van 'n kantoorwerker. Metodes: „n N=1 studie was uitgevoer deur gebruik te maak van die ABC ontwerp. Etiese goedkeuring was verkry vir die studie en die deelnemer het ingeligte skriftelike toestemming verleen. Die deelnemer was ge-evalueer oor drie vier week-lange fases terwyl sy haar gewone rekenaarwerk verrig het. Die uitkomsmetings ge-evalueer tydens die drie fases was pyn intensiteit en waargenome sitgemak. Die drie fases was genoem die basislyn, intervensie en uitwas fases. Gedurende die basislyn fase was die uitkomsmetings by die deelnemer se gewone werkstasie ingevorder. Die intervensie fase het 'n vertikale aanpassing van die stoel en rekenaarskerm behels. Die uitwas fase het die deelnemer toegelaat om haar stoel en rekenaarskerm se hoogte aan te pas volgens haar keuse. 'n Opvolg onderhoud was gevoer met die deelnemer drie maande na die voltooiing van die studie. Die resultate was vasgelê op 'n Microsoft Excel 2010 data bladsy, waarna die data getabuleer en grafies uitgebeeld is. Resultate: Die gemiddelde pyn intensiteit van die deelnermer het effens toegeneem tydens die intervensie fase in vergelyking met die basislyn fase, maar het stabiel gebly tydens die uitwas fase. Die gemiddelde waargenome sitgemak het aanvanklik verswak tydens die intervensie fase, maar het later verbeter tydens die intervensie fase en het aangehou verbeter tydens die uitwas fase. Die waargenome sitgemak het groter verbetering getoon as die pyn intensiteit tydens die uitwas fase. Beide pyn intensiteit en waargenome sitgemak het verbetering getoon by die drie maande opvolg evaluasie, na voltooiing van die studie. Gevolgtrekking. Die vertikale hoogte aanpassing van die stoel en rekenaarskerm het nie die deelnemer se pyn intensiteit en waargenome sitgemak in vergelyking met die deelnemer se gewone werkstasie parameters verbeter nie. Hierdie bevindinge is nie ten voordeel van die horisontale kykhoek nie. Nietemin, ondersteun die bevindinge van hierdie studie die gebruik van die "effens onder die horisontale" kykhoek as bevorderend om die pyn intensiteit te verminder en die sitgemak van 'n kantoorwerker te verbeter.

INTRODUÇÃO: O tratamento com ondas de choque (TOC) é utilizado para tratar numerosas afecções musculoesqueléticas, incluindo-se as pseudartroses e as tendinopatias. Há poucos estudos bem estruturados sobre a eficácia do TOC no tratamento da síndrome dolorosa miofascial (SDM) e não há ensaio clínico aleatorizado sobre sua utilização no tratamento das SDMs das regiões lombar e glútea. OBJETIVOS: Avaliar a eficácia do TOC no tratamento das SDMs das regiões lombar e glútea. CASUÍSTICA E MÉTODOS: Foi realizado estudo prospectivo, controlado, com amostra aleatória e duplamente encoberto sobre o tratamento de doentes com dor moderada a intensa decorrente de SDM nas regiões lombar e glútea com duração superior a seis meses, submetidos previamente a tratamento padronizado com antidepressivo, analgésico, terapia física e orientações fisioterápicas durante seis semanas. Foram elegíveis 46 doentes que apresentavam dor com intensidade >= 4 de acordo com a EVA dentre os 121 convocados. Durante seis semanas os doentes elegíveis foram submetidos a tratamento farmacológico e fisioterápico padronizado. Sete doentes usufruíram melhora clínica importante e oito abandonaram o estudo, restando 31 doentes que participaram efetivamente do estudo. Após a randomização, 14 doentes foram submetidos a TOC com cabeçote ativo e 17 a TOC com cabeçote placebo. Foram avaliados os aspectos demográficos, a apresentação clínica, a incapacidade funcional, a intensidade e as características da dor até um ano após a realização dos procedimentos destes 31 doentes. As avaliações foram realizadas com uso da Escala Visual Analógica (EVA), Questionário de Incapacidade de Roland-Morris (RDQ), Índice de Incapacidade de Oswestry (ODI), Versão Reduzida do Questionário de Dor McGill (SF-MPQ) e Inventário Diagnóstico da Dor Neuropática 4 (DN4). RESULTADOS: Não houve diferenças estatisticamente significativas entre os grupos quanto às características sociodemográficas dos doentes. Entretanto, a duração das queixas de dor dos doentes do grupo TOC ativo foi significativamente superior (p < 0,05) a dos do grupo TOC placebo. Em relação aos doentes tratados com TOC placebo, os doentes tratados com TOC ativo usufruíram redução estatisticamente significativa da dor de acordo com a EVA na interação grupo versus tempo a partir do momento \"três meses\"; a melhora manteve-se estatisticamente significativa durante um ano (p < 0,001), achado que sugere que o efeito analgésico instala-se em longo prazo e mantém-se prolongadamente. Não ocorreu modificação estatisticamente significativa na interação grupo versus tempo nas pontuações dos questionários RDQ, ODI e SF-MPQ ao longo do tempo nos doentes de ambos grupos. No momento \"12 meses\" ocorreu redução superior a 50% da incapacidade funcional da dor lombar avaliada de acordo com o RDQ em 70,0% dos doentes do grupo TOC ativo e em apenas 14,3% dos doentes tratados com TOC placebo; diferença percentual estatisticamente significativa (p < 0,05). Ocorreu também redução superior a 50% das pontuações do ODI na avaliação realizada no momento \"12 meses\" em 70,0% dos doentes incluídos no grupo TOC ativo e em apenas 14,3% dos doentes do grupo TOC placebo, diferença percentual estatisticamente significativa (p < 0,05). CONCLUSÕES: O tratamento com o TOC ativo dos doentes com SDM nas regiões lombar e glútea proporcionou melhora significativa da dor a partir do momento \"três meses\" até, pelo menos, o momento \"12 meses\" de acompanhamento, achado que sugere que seu efeito analgésico instala-se tardiamente. Adicionalmente, proporcionou melhora da funcionalidade de acordo com o RDQ e ODI na avaliação realizada no momento \"12 meses\" / INTRODUCTION: Extracorporeal shockwave therapy (ESWT) has been used successfully in different musculoskeletal conditions, including pseudarthrosis and tendinopathies. However, there are very few well-structured studies on the efficacy of ESWT in the treatment of myofascial pain syndromes (MPSs) and no randomized clinical trial about the ESWT in the treatment of lumbar and gluteal myofascial pain. OBJECTIVES: To assess the efficacy of ESWT in the treatment of lumbar and gluteal MPSs. MATERIAL AND METHODS: The study was prospective, randomized, double-blind and placebo-controlled. From 121 patients with moderate or severe pain due to MPS in the lumbar and gluteal regions lasting more than six months were enrolled; a total of 46 patients with pain intensity >= 4 according to the VAS were considered eligible. The elected patients were treated with antidepressant, analgesic and physical therapy as a standard protocol during six weeks. Seven patients had significant clinical improvement with the pharmacological and physical therapies and eight dropped out the study. The remainder 31 patients were randomized and 14 underwent active ESWT and 17 underwent placebo ESWT. The demographic aspects, clinical presentations, functional disabilities, severity and characteristics of pain were evaluated previously to the inclusion in the study until the end of the first year after the treatment with active or placebo ESWT. The evaluations were based on the Visual Analogue Scale (VAS), Roland- Morris Disability Questionnaire (RDQ), Oswestry Disability Index (ODI), Short- Form of the McGill Pain Questionnaire (SF-MPQ), and the Neuropathic Pain Diagnostic Questionnaire 4 (DN4). RESULTS: There were no statistical differences between the groups regarding the baseline characteristics of the patients. However, the duration of pain of the patients treated with active ESWT was significantly higher (p < 0,05) than those treated with placebo ESWT. There was no statistically significant variation over time in the RDQ, ODI and SF-MPQ scores between the patients from each group. Patients treated with active ESWT presented a significant reduction of pain severity according to the VAS from the third until the 12nd month of follow-up (p < 0,001), finding indicative that the analgesic effect of the ESWT starts late but remains over time. At the 12nd month of follow-up, 70,0% of the patients treated with active ESWT and just 14.3% of the patients from de placebo ESWT group had more than 50% improvement of the functional disability of the low back pain according to the RDQ, statistically significant difference (p < 0,05). There was also a reduction of more than 50% of ODI scores in the 12th month of follow-up in 70.0% of the patients treated with active ESWT and in only 14.3% of the patients treated with placebo ESWT (p < 0,05). CONCLUSIONS: The active ESWT provided a significant and lasting reduction in pain intensity from the third until the 12th month of follow-up, finding that suggests that its analgesic effect settles late and has long duration. Additionally, it provided improvement of the functionality according to the RDQ and ODI at the 12th month of follow-up