INTRODUÇÃO: A rinite alérgica é uma condição clínica comum que apresenta sintomas diversos num significante número de pacientes, deteriorando a qualidade de vida daqueles refratários aos tratamentos usuais (anti-histamínicos e corticosteróides nasais tópicos). Apresentando princípios curativos similares, a imunoterapia sublingual e a homeopatia podem reduzir os sintomas e a necessidade de medicamentos na rinite alérgica, embora a eficácia e a efetividade de ambas terapêuticas não sejam ainda suficientemente conhecidas. OBJETIVOS: O objetivo deste estudo foi avaliar a efetividade clínica do tratamento homeopático individualizado prolongado, comparativamente ao placebo, em adultos portadores de rinite alérgica perene. MÉTODOS: Um total de 41 pacientes com rinite alérgica perene foi alocado numa primeira fase duplo-cego e placebo-controlada durante seis meses, sendo tratada com doses sublinguais semanais de medicamentos homeopáticos individualizados ou placebo. Após esta fase inicial fechada, todos os pacientes foram convidados a participar de uma segunda fase controlada aberta, em que receberiam tratamento homeopático pelo período máximo de 36 meses, e os resultados foram comparados com a melhora da fase inicial. O escore dos sinais e sintomas, a necessidade de medicamentos de resgate e a qualidade de vida foram mensurados por questionários e avaliações clínicas pessoais, aplicadas por um mesmo avaliador independente, antes e após cada fase. As doses dos medicamentos homeopáticos e de resgate utilizados, assim como os efeitos colaterais, foram documentados num diário pessoal. Os desfechos clínicos primário e secundários foram, respectivamente, os escores dos sinais e sintomas alérgicos específicos e gerais. Títulos da IgE total foram mensurados antes e após cada fase. RESULTADOS: Após os seis meses da fase placebo-controlada inicial, na análise por protocolo de todos os pacientes incluídos no estudo, não foram observadas diferenças significativas entre os grupos ativo e placebo nos escores clínicos, na utilização de drogas de resgate, na qualidade de vida e nos títulos da IgE total. Entretanto, as análises dos subgrupos da segunda fase mostraram uma crescente e significativa melhora nos desfechos clínicos primário e secundários após 12 meses de tratamento homeopático individualizado, comparativamente à variação de melhora dos mesmos pacientes na fase inicial fechada. Diferença significativa na qualidade de vida foi observada apenas após o segundo ano de tratamento homeopático. CONCLUSÃO: Neste estudo, o tratamento homeopático foi acompanhado de um significante efeito placebo. A efetividade da homeopatia pôde ser observada após 12 meses da terapêutica, apresentando efeito preventivo de longa duração após 36 meses de tratamento homeopático individualizado. / INTRODUCTION: Allergic rhinitis is a common clinical condition which presented several symptoms in a significant number of patients, deteriorating the quality of life in those resistant to the usual treatments (antihistamines and topical nasal corticosteroids). Presenting similar curative principles, sublingual immunotherapy and homeopathy can reduce symptoms and medication requirements in allergic rhinitis, although the efficacy and effectiveness of both therapeutics are not still sufficiently known. OBJECTIVES: The objective of this study was to evaluate clinical effectiveness of prolonged individualized homeopathic treatment, compared with placebo, in adults with perennial allergic rhinitis. METHODS: A total of 41 adults with perennial allergic rhinitis were enrolled in a first double-blind placebo-controlled phase for six months, and treated on a weekly basis with sublingual doses of single individualized homeopathic medicines or placebo. After this closed initial phase, all patients were invited to participate in an open label controlled phase, in that they would receive homeopathic treatment for the maximum period of 36 months, and the results were compared with the improvement of the initial phase. Signs and symptoms scores, rescue medication requirements and quality of life were assessed by questionnaires and personal clinical evaluation by a same independent researcher, before and after each phase. Applied homeopathic and rescue drugs dosage, and side effects were documented by diary cards. Primary and secondary clinical outcome were, respectively, specific and general allergic signs and symptoms scores. Total IgE titles were performed before and after each phase. RESULTS: After six months of placebo-controlled phase, analyzing all patients included in the study per protocol, we observed no significant difference between treatment and placebo groups in primary and secondary clinical outcomes, use of rescue drugs, quality of life and total IgE. However, second phase subgroups analysis showed a significant and growing improvement of clinical symptoms after 12 months of individualized homeopathic treatment, comparatively to the same patients\' variation in closed initial phase. Significant difference in quality of life score were observed only after second homeopathic treatment year. CONCLUSION: In this study, homeopathic treatment was accompanied by a significant placebo effect. Effectiveness of homeopathy could be seen after 12 months of therapy, presenting preventive effect of long duration after 36 months of individualized homeopathic treatment.

Sehnenverletzungen machen ca. 30 % der muskuloskelettalen Beschwerden aus. Repetitive Überlastung wird häufig als Ursache diskutiert. Dabei entstehende strukturelle Schäden können die Kapazität der Sehne, mechanische Belastung zu tolerieren, reduzieren. Das exzentrische Protokoll nach Alfredson sowie das „heavy slow resistance training“ sind häufig genutzte Formen der Trainingstherapie. Jedoch zeigen diese Protokolle bisher kaum Nachweise für strukturelle Anpassung. Eine trainingsinduzierte Zunahme der Sehnensteifigkeit könnte die Sehne widerstandsfähiger machen und vor Überlastung schützen, da die Beanspruchung (Sehnendehnung) bei gegebener Belastung reduziert wird. Bei gesunden Probanden führte das „high-loading“ Protokoll, das mit einer hohen Dehnungsmagnitude arbeitet, ausgelöst durch ca. 90 % der maximal willkürlichen Kontraktionskraft der Plantarflexoren, sowie einer Dauer von 3 Sek., zu positiven strukturellen Anpassungen. Die vorliegende Arbeit zeigt erstmals, dass sich tendinopathische Achillessehnen bei ausreichend hohem mechanischen Stimulus ähnlich gesunden Sehnen anpassen. Im Vergleich zum exzentrischen Training sowie passiver Therapie führte nur das high-loading Protokoll zu einer Hypertrophie der Sehne sowie einer Zunahme der Sehnensteifigkeit, während es in allen drei Gruppen gleichermaßen zu klinisch-funktionellen Verbesserungen kam. Das dabei angewandte mobile Trainingsgerät bewies in einer separaten Studie exzellente Reliabilität sowie Effektivität (Kraft/Sprunghöhe). Weiters wurden Asymmetrien zwischen der betroffenen/nicht-betroffenen Seite untersucht. Größtenteils zeigten sich im Vergleich zu Gesunden ähnlich ausgeprägte Asymmetrien. Die Effekte auf diese Asymmetrien durch Training waren eher gering. Eine Reduzierung der Asymmetrien ging nicht notwendigerweise einher mit einer klinisch-funktionellen Verbesserung. Insgesamt liefern die Ergebnisse wichtige Erkenntnisse bezüglich einer neuartigen Behandlungsmethode der Achillestendinopathie, die durch die hervorgerufene Verbesserung von Sehneneigenschaften sowohl für die Rehabilitation als auch Prävention zu empfehlen ist. / Tendon injuries account for approximately 30 % of musculoskeletal consultations. Repetitive overload is identified commonly as initial cause implicating structural impairments. Hence, the capacity of the tendon to tolerate mechanical load might be attenuated. In Achilles tendinopathy, Alfredsons ´eccentric exercise protocol and heavy slow resistance training are frequently applied exercise interventions both leading to clinical and functional improvements. However, evidence for eliciting structural adaptation is lacking. An exercise-induced increase in tendon stiffness might improve the tendon `s capacity to tolerate loading and thus reduce future damage as tendon strain at a given force is reduced. In healthy subjects, the high-loading protocol applying high tendon strain induced by highly intensive muscle contractions (i.e., at 90 % of maximum voluntary isometric contraction) with 3 seconds time-under-tension has led to positive adaptations (i.e., increased cross-sectional area and stiffness). This thesis first provides evidence that tendinopathic Achilles tendons do adapt comparable to healthy tendons given that an adequate mechanical stimulus was applied. High-loading led to tendon hypertrophy and an increase in tendon stiffness compared to eccentric exercise or passive therapy, while clinical/functional improvements have been detected in all the three groups. In a separate trial, the applied mobile training device showed excellent reliability and effectiveness (strength/jump height). Further, inter-limb asymmetries have been investigated showing comparable levels except for vascularization compared to healthy subjects. Therapeutic interventions had only small effects regarding pronounced asymmetry reductions whereas a reduction in asymmetry did not necessarily correlate with an improvement in tendon health. In conclusion, the findings of the present thesis provide valuable evidence for high-loading as a novel exercise treatment in Achilles tendinopathy.