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OBJECTIVE: To investigate the effect of diadynamic currents administered prior to exercises on pain and disability in patients with osteoarthritis of the knee. DESIGN: A randomized-controlled trial. SETTING: Special Rehabilitation Services in Taboão da Serra. PARTICIPANTS: Patients with bilateral knee osteoarthritis. INTERVENTION: Participants were randomly allocated to Group I (diadynamic currents and exercises; n = 30, 60 knees) or Group II (exercises alone; n = 30, 60 knees) and were treated three times a week for 8 weeks. MAIN OUTCOME MEASURES: The primary outcome measures were change in knee pain evaluated by visual analog scale and disability Index Score (Lequesne). Secondary outcomes included change in mobility (Timed Up and Go test), range of motion (goniometer), muscle strength (dynamometer), a composite score for pain and disability (Western Ontario and McMaster Universities Osteoarthritis questionnaire), and a drug diary to measure consumption of rescue pain medication (paracetamol). All measurements were collected at baseline, 8 weeks, and 6 months from baseline (follow-up). RESULTS: There were 60 participants with a mean (SD) age of 63.40 (8.20) years. Between-group differences in the follow-up (8 weeks and 6 months) were observed for pain at rest, pain during activities of daily living and disability. There was improvement in Group I that was maintained for the three variables 6 months after treatment. Mean difference for pain at rest was -3.08 points (95% confidence interval -4.13; -2.02), p < 0.01 with an effect size of 1.4; mean difference for pain during activities of daily living was -2.40 points (95% confidence interval -3.34; -1.45), p < 0.01 with an effect size of 1.24; and mean difference for disability was -4.08 points (95% confidence interval -5.89; -2.26), p < 0.01 with an effect size of 1.04. CONCLUSION: Patients with symptomatic knee osteoarthritis receiving 8 weeks of treatment with diadynamic currents as an adjunct to a program of exercises had significantly greater improvements in pain and disability than those receiving exercises alone. Beneficial effects were sustained for 6 months.

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ABSTRACT BACKGROUND AND OBJECTIVES: The purpose of this study was to evaluate the effectiveness of Transcutaneous Electrical Nerve Stimulation (TENS) combined with manual therapy in women diagnosed with muscular Temporomandibular Dysfunction (TMD) with or without Reduced Disc Displacement (RDD). The objective was to evaluate the action of manual therapy in conjunction with TENS as a therapeutic tool for treating TMD, analyzing the electromyographic tasks in MVC and in rest, and measuring pain scores with the Visual Analog Scale (VAS). METHODS: This study has a blinded randomized clinical trial design. In this context, after screening, 11 women with a diagnosis of muscular TMD with or without RDD, aged between 18 and 39 years, were investigated. The 11 women were randomly divided into two intervention groups, one receiving manual therapy alone and the other receiving manual therapy together with TENS. The participants were assessed using the Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) and MBGR protocols for inclusion and exclusion, using the VAS to analyze pain, and Surface Electromyography (EMG) to analyze MVC and rest muscle activation. RESULTS: Lower MVC and rest values were observed after the intervention in both intervention groups. Manual therapy alone was as effective as manual therapy combined with TENS. There was no difference between the manual therapy group (MG) and manual therapy+TENS group (TG) in the VAS scores, however when comparing pre- and post-intervention, lower values were observed in the scores of both groups. CONCLUSION: Both groups showed a reduction in pain, but the combination of TENS and manual therapy showed a slight improvement in the stability of the masticatory muscles compared to manual therapy alone. With or without TENS, muscle relaxation and analgesia were achieved.

RESUMO JUSTIFICATIVA E OBJETIVOS: Esta pesquisa teve o propósito de avaliar a eficácia da Estimulação Elétrica Nervosa Transcutânea (TENS) combinada com terapia manual em mulheres diagnosticadas com Disfunção Temporomandibular (DTM) muscular com ou sem Deslocamento de Disco com Redução (DDR). O objetivo foi avaliar a ação da terapia manual em conjunto com a TENS como ferramenta terapêutica para tratamentos da DTM, analisando as tarefas eletromiográficas na Contração Voluntária Máxima (CVM) e no repouso, e aferindo os escores da dor com a Escala Analógica Visual (EAV). MÉTODOS: Este estudo possui um desenho de ensaio clínico randomizado cego. No contexto, após a triagem foram investigadas 11 mulheres com diagnóstico de DTM muscular com ou sem DDR, com idades entre 18 e 39 anos. As 11 mulheres foram divididas randomicamente em dois grupos de intervenção, um deles recebendo somente terapia manual e outro grupo recebendo a terapia manual juntamente com a TENS. As participantes foram avaliadas pelos protocolos Critérios de Diagnóstico para Desordens Temporomandibulares (DC/TMD) e MBGR para inclusão e exclusão, por meio da EAV para análise da dor, e da Eletromiografia de Superfície (EMG) para a análise da CVM e do repouso, verificando a ativação muscular. RESULTADOS: Foram observados menores valores da CVM e de repouso após a intervenção em ambos os grupos de intervenção. A aplicação só de terapia manual é tão eficaz quanto o uso de terapia manual em conjunto com a TENS. Não houve diferença entre o grupo com terapia manual (GM) e o grupo com terapia manual+TENS (GT) nos escores da EAV, entretanto quando comparados pré e pós-intervenção, foram observados menores valores nos escores dos dois grupos. CONCLUSÃO: Ambos os grupos apresentaram redução da dor, mas a combinação de TENS e terapia manual mostrou ligeira melhora na estabilidade da musculatura mastigatória em comparação com a terapia manual isolada. Com ou sem TENS, o relaxamento muscular e a analgesia foram alcançados.

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ABSTRACT BACKGROUND AND OBJECTIVES: Neuropathic pain (NP) affects the afferent somatosensory pathways, generating various symptoms, however, there is difficulty in terms of diagnosis and in the formation of treatment protocols. There is a need to search the current literature for effective resources for the treatment of peripheral neuropathy in rehabilitation. The objective of this study was to describe reproducible assessment and treatment approaches capable of reducing NP. CONTENTS: Full articles produced between 2018 and 2022, found in the Pubmed, Scielo, Medline, Embase and Cochrane databases were included. Fifteen Boolean descriptors were used, and data were cross-referenced with the words "AND" or "OR". The selected articles went through the Methodi Ordinatio of classification and organization of studies. Eleven articles were selected and used in this review, two from 2018, five from 2020, and three from 2021. Regarding the type of study, five review articles, one case study, and six intervention studies were obtained. Of these 11 studies, only three used quality of life (QoL) indicators. Most studies used combined interventions, and in more than half of the publications transcranial direct current stimulation (tDCS) was present. The somatosensory rehabilitation method was able to redeem neuropathy through specific techniques. CONCLUSION: The implications of the neuropathic pain treatment in terms of QoL were left in the background by the bibliometric survey carried out. It is suggested that new studies could associate analgesia techniques with rehabilitation methods, including and measuring the effects on the QoL of these patients.

RESUMO JUSTIFICATIVA E OBJETIVOS: A dor neuropática (DN) acomete as vias somatossensoriais aferentes, gerando diversos sintomas, entretanto há dificuldades em termos de diagnóstico e na formação de protocolos de tratamento. Há a necessidade de buscar, na literatura atual, recursos eficazes para o tratamento da neuropatia periférica na área da reabilitação. O objetivo deste estudo foi descrever abordagens reprodutíveis de avaliação e tratamento capazes de diminuir a DN. CONTEÚDO: Foram incluídos artigos completos produzidos entre os anos de 2018 e 2022, encontrados nos bancos de dados Pubmed, Scielo, Medline, Embase e Cochrane. Foram usados 15 descritores booleanos, e os dados foram cruzados com as palavras "AND" ou "OR". Os artigos passaram pelo Methodi Ordinatio de classificação e organização de estudos. Foram selecionados e utilizados 11 artigos, sendo dois de 2018, cinco de 2020 e três de 2021. Acerca do tipo de estudo, foram obtidos cinco artigos de revisão, um estudo de caso e seis estudos de intervenção. Desses 11 estudos, apenas três utilizaram indicadores de qualidade de vida (QV). A maioria dos estudos utilizou intervenções combinadas, e em mais da metade das publicações a estimulação transcraniana por corrente contínua (ETCC) estava presente. O método de reabilitação somatossensorial foi capaz de redimir a neuropatia por meio de técnicas específicas. CONCLUSÃO: As implicações do tratamento da dor neuropática no quesito QV ficaram em segundo plano pelo levantamento bibliométrico realizado. Sugere-se que novos estudos possam associar técnicas de analgesia a métodos de reabilitação, incluindo e mensurando os efeitos sobre a QV desses pacientes.

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Introduction Temporomandibular joint disorders (TMD) present with a multitude of symptoms that can range from headaches to shoulder pain. Patients frequently present with pain in the ear, dizziness, and vertigo. It is noted that some patients who report TMDs also have a history of sleep disturbances, which is noted in cone beam computed tomography (CBCT) as a reduction in the oropharyngeal airway volume. Objective To evaluate the airway volume in pre- and posttreatment of TMD with the use of neuromuscular orthotics made with ultra-low frequency transcutaneous electrical nerve stimulation (ULF-TENS). Methods A total of 15 patients were evaluated for TMDs using the related criteria. Those included were treated with ULF-TENS with evaluation of the airway volume both pre- and posttreatment using CBCT and the Dolphin 3D volume analysis software. Results While the symptoms were shown to be significantly reduced in patients who were treated with this particular modality, the airway volume varied in those who reported a reduction after a period of 3 months and those that reported after a period of 6 months. Conclusion Posttreatment evaluation of the airway should be done after a period of 6 months for a more objective evaluation. A multidisciplinary evaluation of the patient is required in such cases.

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OBJECTIVE: To compare the effect of photobiomodulation (PBM) and transcutaneous electrical nerve stimulation (TENS) in the treatment of burning mouth. MATERIALS AND METHODS: Randomized clinical trial of 25 patients with burning mouth treated by TENS (n=12) and PBM (n=13). The patients were treated weekly for 8 weeks. Two-factor ANOVA was used to determine whether the two interventions promoted significant differences in symptoms (measured with a visual analogue scale), unstimulated salivary flow, xerostomia, and dysgeusia between T0 (baseline), T1 (after the 4th treatment session), T2 (after the 8th treatment session), and T3 (30 days after the end of treatment). RESULTS: Intragroup comparison of VAS scores for pain showed a significant difference between T0xT1, T0xT2, and T0xT3 in the TENS group and between T0xT2 and T0xT3 in the PBM group (p˂0.001). Intergroup comparison of VAS scores for pain between T2xT3 showed a better response to PBM than to TENS (p=0.003). Patients of the TENS group showed an increase in salivary flow between T1 and T2 (p=0.052). There were no expressive variations in xerostomia or dysgeusia in the two groups analyzed. CONCLUSION: TENS and PBM were effective in reducing the symptoms of burning mouth during and after treatment. The PBM group showed a better response during follow-up. TRIAL REGISTRATION: This clinical trial was registered at http://clinicaltrials.gov (Number: NCT05816200). CLINICAL RELEVANCE: TENS was found to be a safe and effective therapy for burning mouth. Trial registration number (TRN) and date of registration: This clinical trial was registered at http://clinicaltrials.gov (Number: NCT05816200; date: May 08, 2023).

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BACKGROUND: Several systemic conditions can result in distinct degrees of salivary gland damage and consequent hypofunction. The development of successful management schemes is highly challenging due to the complexity of saliva. This study aimed to systematically map the literature on the physical stimulation of salivary glands for hyposalivation management and the response of individuals according to different systemic conditions causing salivary impairment. METHODS: A systematic search in the literature was performed. Two reviewers independently selected clinical trials, randomized or not, that used physical stimulation to treat hyposalivation caused by systemic conditions. Studies evaluating healthy subjects without hyposalivation were included as controls. Single-arm clinical studies or case series were also included for protocol mapping (PRISMA extension for scoping reviews). RESULTS: Out of 24 included studies, 10 evaluated healthy subjects, from which 9 tested transcutaneous electrical nerve stimulation (TENS) and 1 tested acupuncture and electroacupuncture. Fourteen studies evaluated individuals with hyposalivation: 6 applied TENS, 6 applied low-level laser therapy (LLLT), and 2 applied acupuncture, carried out in post-chemotherapy, medication use, postmenopausal women, hemodialysis patients, smokers, diabetics, Sjögren's syndrome (SS). All showed increased salivation after treatment, except for two LLLT studies in individuals with SS. CONCLUSIONS: Among the different patient groups, individuals with Sjögren's syndrome (SS) exhibited the poorest responses, while those with medication-induced hyposalivation demonstrated the most favorable treatment outcomes, independently of the management strategy for saliva stimulation. It means that physical stimulation of salivary glands holds promise as an alternative for managing hyposalivation in cases of reversible gland damage. However, to make informed decisions in current practice, it is necessary to conduct new well-designed randomized clinical trials with appropriate methodologies.

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ABSTRACT BACKGROUND AND OBJECTIVES: Despite the widespread use of mid-frequency currents in reducing pain in chronic low back pain (CLBP), there is still no consensus on the optimal parameters for treatment. The aim of this study was to compare the immediate analgesic effects of interferential (IC) and Aussie (AC) currents in CLBP. METHODS: This is a five-arm double-blind randomized controlled trial. Patients aged between 18 and 60 years with CLBP were randomly divided into 5 groups: CI4kHz/100Hz, CI4kHz/2Hz, CA4kHz/100Hz, CA4kHz/2Hz and placebo (PG). Participants received a single application of Interferential current or Aussie current for 30 min. Main outcome measures were pain intensity by numeric pain scale (NPS), McGill pain questionnaire (MPQ) and pressure pain threshold. The secondary outcomes assessed were: abdominal strength test (AST), lumbar flexion test (modified Schober test), trunk and lower limb mobility (sit and reach test and finger tip test). RESULTS: There was a significant difference in NPS and MPQ groups (with the exception of the affective component) (p<0.05) in IC 4 kHz/100 Hz and IC 4 kHz/2 Hz groups in relation to PG. Regarding secondary outcomes, a difference was found only between IC 4kHz/2Hz and PG in AET. CONCLUSION: Interferential current, regardless of frequency modulation, provided immediate analgesic effect in individuals with CLBP, being superior to the effects of Aussie current.

RESUMO JUSTIFICATIVA E OBJETIVOS: Apesar da grande utilização das correntes de média frequência na diminuição do quadro álgico na dor lombar crônica (DLC), ainda não existe consenso sobre os parâmetros ideais para tratamento. O objetivo deste estudo foi comparar os efeitos analgésicos imediatos das correntes interferencial (CI) e Aussie (CA) na DLC. MÉTODOS: Trata-se de um ensaio clínico randomizado controlado duplo-cego de cinco braços. Foram selecionados pacientes com idades entre 18 e 60 anos, com DLC, que foram divididos aleatoriamente em 5 grupos: CI4kHz/100Hz, CI4kHz/2Hz, CA4kHz/100Hz, CA4kHz/2Hz e placebo (GP). Os participantes receberam uma única aplicação da corrente Interferencial ou corrente Aussie durante 30 min. As principais medidas de desfechos foram: intensidade da dor pela escala numérica da dor (END), questionário de dor McGill (QDM) e limiar de dor por pressão. Os desfechos secundários avaliados foram: teste de resistência abdominal (TRA), teste de flexão da lombar (teste de Schober modificado), mobilidade de tronco e membros inferiores (teste de sentar e alcançar e teste de distância do terceiro dedo ao solo). RESULTADOS: Houve diferença significativa nos grupos END e QDM (com exceção do componente afetivo) (p<0,05) nos grupos CI 4 kHz/100 Hz e CI 4 kHz/2 Hz em relação ao GP. Com relação aos desfechos secundários foi encontrada diferença somente entre CI 4kHz/2Hz e GP no TRA. CONCLUSÃO: A corrente interferencial, independente da modulação da frequência, proporcionou efeito analgésico imediato em indivíduos com DLC, sendo superior aos efeitos da corrente Aussie.

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OBJECTIVE: To assess the efficacy of vaginal electrical stimulation (VS) versus transcutaneous tibial nerve electrical stimulation (TTNS) in women with overactive bladder syndrome (OAB). MATERIAL AND METHODS: Sixty-nine patients were randomized to receive 12 sessions of VS versus TTNS, or no treatment (control group-CG), over 6 weeks. OAB impact according to international consultation on incontinence questionnaire overactive bladder module (ICIQ-OAB), symptoms discomfort scores and voiding diaries were evaluated at baseline, 6 weeks and 1-month post-treatment. RESULTS: Both TTNS (mean difference = -4.2; 95% confidence interval [CI] = -6.5 to -1.9) and VS (-3.8; -6.0 to -1.6) were associated with significant reduction of ICIQ-OAB scores, as well as discomfort sensation (-3.9; -6.2 to -1,7; p < 0.001 for the TTNS and -2.8; -5.0 to -0.6; p = 0.01 for the VS) at 6 weeks when compared to CG (p < 0.001). ICIQ-OAB score remained low only in the TTNS group when compared to the CG (-3.6; -6.0 to -1.2/p = 0.00) 1 month after treatment. Discomfort symptoms improved in both active groups when compared to CG (TTNS [-3.2; -5.2 to -1.2; p < 0.001] and VS groups [-2.6; -4.7 to -0.6; p = 0.01]). No statistically differences were found in primary outcomes comparing TTNS and VS Secondary analysis showed significant improvement in urinary urgency incontinence episodes (UUI) in both TTNS and VS, but CG. UUI episodes were still reduced in the VS group and urgency in the TTNS group 1-month post-treatment. CONCLUSION: Short-term interventions (6 weeks) of TTNS and VS were both effective in treating women with OAB. TTNS provided residual effects at one-month postintervention on ICIQ-OAB score.

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Abstract Introduction Temporomandibular joint disorders (TMD) present with a multitude of symptoms that can range from headaches to shoulder pain. Patients frequently present with pain in the ear, dizziness, and vertigo. It is noted that some patients who report TMDs also have a history of sleep disturbances, which is noted in cone beam computed tomography (CBCT) as a reduction in the oropharyngeal airway volume. Objective To evaluate the airway volume in pre- and posttreatment of TMD with the use of neuromuscular orthotics made with ultra-low frequency transcutaneous electrical nerve stimulation (ULF-TENS). Methods A total of 15 patients were evaluated for TMDs using the related criteria. Those included were treated with ULF-TENS with evaluation of the airway volume both pre- and posttreatment using CBCT and the Dolphin 3D volume analysis software. Results While the symptoms were shown to be significantly reduced in patients who were treated with this particular modality, the airway volume varied in those who reported a reduction after a period of 3 months and those that reported after a period of 6 months. Conclusion Posttreatment evaluation of the airway should be done after a period of 6 months for a more objective evaluation. A multidisciplinary evaluation of the patient is required in such cases.

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OBJECTIVE: To assess the impact of parasacral transcutaneous electrical nerve stimulation (parasacral TENS) on quality of life (QoL) and psychological aspects in children treated for overactive bladder (OAB). METHODS: This international, multicenter, prospective cohort study involved individuals of 6-16 years of age under TENS treatment for OAB. The study was conducted between June 2016 and December 2019 in four participating centers: two in Australia, one in Germany and one in Brazil. Patients with anatomical and/or neurological abnormalities of the urinary tract were excluded. Questionnaires were applied before and after parasacral TENS treatment: the Dysfunctional Voiding Symptom Score (DVSS), used in Brazil, or the International Consultation on Incontinence Questionnaire - Pediatric Lower Urinary Tract Symptoms (ICIQ-CLUTS), used in Germany and Australia, to analyze urinary symptoms; the Strengths and Difficulties Questionnaire (SDQ) to assess emotional and behavioral aspects; and the Pediatric Incontinence Questionnaire (PinQ) for bladder-specific Qol. RESULTS: Fifty-three patients (28 girls and 25 boys) with a mean age of 8.64 ± 2.63 years were included. Median DVSS was 11 (range 6-13.5) and 3 (range 0-7), (p < 0.001), and median ICIQ-CLUTS was 12 (range 9-14) and 9 (range 5.7-12), (p < 0.001), before and after treatment, respectively. Median PinQ score decreased from 47.8 (range 38.9-59.7) to 39 (range 29-53.15) following treatment (p = 0.04). Median total SDQ score before and after treatment was 17 (range 13.5-21) and 15 (range 12-21), respectively (p = 0.939). CONCLUSION: Parasacral TENS was associated with a significant improvement in urinary symptoms and QoL; however, there was no change in psychological symptoms, as measured using the SDQ.

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Objective: to compare the immediate effects of low-frequency TENS employment on vocal quality in women with behavioral dysphonia before and after vocal exercises.Methodology: 30 women (mean = 31.3 years old), diagnosed with behavioral dysphonia received low-frequency TENS before (TENS + VE Group) and after vocal exercises (VE + TENS Group) with a 1-week washout. They had their sustained vowel/a/and running speech recorded before and after each procedure for auditory-perceptual analysis and acoustic measures. The low-frequency TENS parameters applied were symmetrical biphasic quadratic pulse, 200 µs phase, 10 Hz frequency, intensity on the motor threshold, and the electrodes were positioned on the submandibular and superior fibers of the trapezius muscle region. The vocal exercises: tongue trill, humming, finger kazoo, and water resistance therapy were performed totalizing 20 min.Results: intragroup analysis of sustained vowel/a/showed reduction in both groups of strain parameter and increased the breathiness; only VE + TENS Group increased the instability parameter, decreased fundamental frequency, and increased in SPI values; the running speech analysis showed an increase in the overall degree, roughness, and breathiness parameters. However, in VE + TENS Group, there was a statistically significant decrease in the intensity of the strain and an increase in breathiness. The acoustic measures showed that VE + TENS Group had a higher variation than TENS + VE Group regarding NHR.Conclusion: vocal exercises followed by low-frequency TENS have more immediate positive effects on voice quality than the low-frequency TENS followed by vocal exercises. This is a preliminary immediate effects study, and these effects could be verified through long-term assessments.

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INTRODUCTION AND HYPOTHESIS: Electrical nerve stimulation is a widely used treatment for overactive bladder but there is no consensus regarding the best placement of electrodes or protocols. We hypothesised that some non-implanted neurostimulation protocols would be more effective compared to others for treating urinary symptoms and improving quality of life among adults diagnosed with non-neurogenic overactive bladder. METHODS: A systematic review and meta-analyses of randomized clinical trials were performed in five electronic databases: PubMed/MEDLINE, Lilacs, CINAHL, Web of Science, and PEDro. The main outcome was urinary symptoms-frequency, nocturia, and urgency-and the secondary outcome quality of life. Some protocol characteristics were extracted, e.g., frequency, pulse width, intensity, intervention time, and electrode placement. RESULTS: Nine randomized controlled trials were included. Tibial neurostimulation showed better results than sacral neurostimulation for urge incontinence (mean difference = 1.25 episodes, 95% CI, 0.12-2.38, n = 73). On the pooled analysis, the different neurostimulation protocols-intravaginal, percutaneous tibial, and transcutaneous tibial nerve stimulation-demonstrated similar results for urinary frequency, nocturia, and urgency as well as quality of life. In general, effect sizes from meta-analyses were low to moderate. The best reported parameters for percutaneous tibial nerve stimulation were 20-Hz frequency and 200-µs width, once a week. CONCLUSIONS: There was evidence that tibial neurostimulation is more effective than sacral neurostimulation for urge incontinence symptoms among patients with non-neurogenic overactive bladder. Overall, there was no superiority of an electrical nerve stimulation electrode placement and protocol over others considering urinary symptoms and quality of life. Further studies with three-arm trials are necessary. This study was registered at PROSPERO: CRD4201810071.

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INTRODUCTION: Postherpetic neuralgia (PHN) is a complex neuropathic painful condition in which pain is a direct consequence of the response to peripheral nerve damage experienced during herpes zoster attack. PHN is the most common chronic complication of herpes zoster and it causes considerable suffering, affecting the physical functioning and psychological well-being of patients. OBJECTIVE: To describe the effect of a conservative treatment using pain neuroscience education (PNE) and transcutaneous electrical nerve stimulation (TENS) in a patient with trigeminal PHN. CASE DESCRIPTION: A 67-year-old woman sought care for pain, dysfunction, and sensory loss in the left jaw. The assessment included: 1) pain, using the numerical pain rating scale (NPRS), pressure pain threshold (PPT), Douleur Neuropathique 4 (DN4), McGill Pain Questionnaire (MPQ), Graded Chronic Pain Scale (GCPS), and classic body charts of the cranial region; 2) somatosensory function, by means of mechanical detection threshold (MDT) and pressure pain threshold (PPT); 3) jaw function, using the Jaw Functional Limitation Scale-20 (JFLS-20); and 4) psychosocial features, by means of the Patient Health Questionnaire-9 (PHQ-9) and the Generalized Anxiety Disorders Questionnaire-7 (GAD-7). Treatment consisted of 12 sessions of PNE and TENS. OUTCOMES: After treatment, a clinically significant improvement in NPRS, DN4, MDT, GCPS, and PHQ-9 was observed. CONCLUSION: In this case report, a treatment based on the combination of PNE and TENS seemed to have contributed to improving pain, sensory abnormalities, and jaw function. Psychosocial factors also showed a trend to improve after the treatment.

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ABSTRACT Objective: To analyze the immediate effect of amplitude modulation frequencies (AMFs) of 4kHz interferential current (IFC) on chronic low back pain (CLBP). Method: This is a randomized controlled clinical trial. Sixty-three subjects with CLBP were recruited. The subjects were randomized into 3 groups: the placebo group (PG, n=21) and 2 intervention groups (IG), IG4kHz/2Hz (n=21) and IG4kHz/100Hz (n=21). All groups were submitted to a single session of 30 minutes. Pain was evaluated using a numerical rating scale (NRS), the McGill Pain Questionnaire (MPQ), and pressure algometry. Flexibility was evaluated using the Modified Schober Test (MST), the Sit-and-Reach Test (SRT), the Fingertip-to-Floor Test (FTF), and the Passive Straight-Leg Raise Test (PSLR). Results: Comparing IG4kHz/100Hz with PG, we found a significant difference (p<0.05) in NRS in the total and in the MPQ categories, whereas in the comparison between IG4kHz/2Hz and PG, we found a significant difference only in the sensory and evaluative categories of MPQ. Regarding the flexibility tests, we observed a significant difference of both IG4kHz/100Hz and IG4kHz/2Hz in comparison to PG in MST and PSLR, and of IG4kHz/2Hz in comparison to PG in SRT. The 4kHz IFC was effective in immediately reducing CLBP and, consequently, in increasing the flexibility of the lumbar spine and lower limbs. Conclusion: Conclusion: There was a greater number of significant positive outcomes when the 100Hz AMF was adopted. Level of Evidence I; High quality randomized clinical trial with or without statistically significant differences, but with narrow confidence intervals.

RESUMO: Objetivo: Analisar o efeito imediato das frequências de modulação de amplitude (AMF) da corrente interferencial (IFC) de 4 kHz sobre dor lombar crônica (DLC). Métodos: Este é um ensaio clínico controlado randomizado. Foram recrutados 63 participantes com DLC. Esses participantes foram randomizados em três grupos: grupo placebo (PG, n = 21) e dois grupos de intervenção (IG), IG4kHz/2 Hz (n = 21) e IG4kHz/100 Hz (n = 21). Todos os grupos foram submetidos a uma única sessão de 30 minutos. A dor foi avaliada por meio de uma escala numérica de classificação (NRS), o questionário de McGill (MPQ) e algometria de pressão. A flexibilidade foi avaliada pelo Teste de Schober Modificado (MST), Teste de sentar e alcançar (SRT), Teste do terceiro dedo ao solo (FTF) e Teste passivo de Elevação de Perna Reta (PSLR). Resultados: Comparando IG4kHz/100 Hz com PG, encontramos diferença significativa (p < 0,05) em NRS nas categorias total e MPQ, enquanto na comparação entre IG4kHz/2Hz e PG, encontramos uma diferença significativa apenas nas categorias sensoriais e de avaliação do MPQ. Com relação aos testes de flexibilidade, observamos diferença significativa tanto do IG4kHz/100 Hz quanto do IG4kHz/2 Hz em comparação com o PG em MST e PSLR, e do IG4kHz/2 Hz em comparação com o PG no SRT. A IFC de 4kHz foi eficaz na redução imediata da DLC e, consequentemente, no aumento da flexibilidade da coluna lombar e dos membros inferiores. Conclusões: Houve maior número de desfechos positivos significativos quando a AMF de 100 Hz foi adotada. Nível de Evidência I; Estudo clínico randomizado de alta qualidade com ou sem diferença estatisticamente significante, mas com intervalos de confiança estreitos.

RESUMEN: Objetivo: Analizar el efecto inmediato de las frecuencias de modulación de amplitud (AMF) de la corriente interferencial (ICF) de 4 kHz sobre el dolor lumbar crónico (DLC). Métodos: Se trata de un ensayo clínico controlad y aleatorizado. Se reclutaron 63 participantes con DLC. Los mismos fueron distribuidos aleatoriamente en 3 grupos: grupo placebo (PG, n=21) y 2 grupos de intervención (IG), IG4kHz/ 2Hz (n=21) e IG4kHz/100 Hz (n=21). Todos los grupos fueron sometidos a una sola sesión de 30 minutos. El dolor se evaluó mediante una escala de clasificación numérica (NRS), el cuestionario de McGill (MPQ) y algometría de presión. La flexibilidad se evaluó mediante el test de Schober modificado (MST), el test de sit-and-reach (SRT), el test de distancia dedos-suelo (FTF) y la prueba pasiva de elevación de la pierna recta (PSLR). Resultados: Al compararIGI4kHz/100 Hz con PG, encontramos una diferencia significativa (p<0,05) en el NRS en las categorías total y MPQ, mientras que en la comparación entre IG4kHz/2 Hz y PG, encontramos una diferencia significativa sólo en las categorías sensoriales y evaluativas de MPQ. En cuanto a las pruebas de flexibilidad, observamos una diferencia significativa tanto de IG4kHz /100 Hz como de IG4kHz/2 Hz en comparación con PG en MST y PSLR, y de IG4kHz/2 Hz en comparación con PG en SRT. La ICF de 4kHz fue eficaz en la reducción inmediata del DLC y, en consecuencia, en el aumento de la flexibilidad de la columna lumbar y los miembros inferiores. Conclusión: Hubo un mayor número de resultados positivos significativos cuando se adoptó la AMF de 100 Hz. Nivel de Evidencia I; Ensayo clínico aleatorizado de alta calidad con o sin diferencia estadísticamente significativa, pero con intervalos de confianza estrechos.

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OBJECTIVE: The objective of this study was to evaluate the analgesic efficacy of a portable, disposable, and home self-applied transcutaneous electrical nerve stimulation (TENS) device during migraine attacks. BACKGROUND: TENS has been used as a noninvasive treatment for migraine, but there are no reports on the outcomes following use of this treatment option for use at home during migraine attacks. DESIGN AND METHODS: A double-blind, randomized controlled trial was conducted over 3 months, with monthly assessments. Active placebos (sham group) were in place and were allocated at a 1:1 ratio. Adult patients who had been diagnosed with migraine by a specialist were included. Pain intensity levels and functional disability were measured before and after the 20-min self-applied TENS intervention during the migraine attacks. RESULTS: Seventy-four participants were randomly allocated to the sham and intervention groups. Although both groups of subjects reported lower pain scores, the intervention group showed a statistically significant reduction in pain scores compared to the sham group. CONCLUSION: In our controlled trial, the use of a self-applied, TENS device is safe and effective in relieving pain associated with migraine attacks. Participants in the intervention group showed a statistically significant improvement in pain and functional disability scores. TENS has been used as a noninvasive treatment for migraine, but there are no reports on the outcomes following use of this treatment option for use at home during migraine attacks. This double-blind, randomized controlled trial had 2 groups: active-placebo and intervention. Seventy-four participants were randomly allocated. Participants in the intervention group showed a statistically significant improvement in pain and functional disability scores.

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A dismenorreia primária é uma dor na região inferior do abdômen, antes ou durante a menstruação e independente de patologias pélvicas. Tratamentos fisioterapêuticos são alternativas para a melhora dos sintomas, dentre esses recursos, a estimulação elétrica nervosa transcutânea (TENS). O objetivo deste estudo foi comparar o efeito terapêutico e analgésico da TENS interativa e convencional na dor secundária à dismenorreia primária. A aplicação da TENS, em ambos os grupos, foi realizada no primeiro dia do período menstrual por 35 minutos. Na TENS interativa todas as voluntárias optaram pelos seguintes parâmetros: frequência de 250 Hz, duração de pulso de 25 µs e intensidade conforme nível sensorial, sendo essa ou a duração do pulso reajustado, a cada 5 minutos, conforme houvesse necessidade. Na TENS convencional foi utilizado os seguintes parâmetros: frequência de 100 Hz, duração de pulso de 50 µs e com a intensidade conforme grupo anterior. A análise estatística foi realizada por meio do software GraphPadPrism®, versão 5.0, sendo empregado o teste t de Student e com nível de significância de p < 0,05. Obteve-se como resultado uma redução da dor entre as participantes de ambos os grupos logo após o tratamento. Porém não houve diferença na analgesia promovida pelos dois métodos de tratamento. (AU)

Primary dysmenorrhea (PD) is a lower region of the abdomen pain, before or during menstruation and independent of pathologies. Physical therapy treatments are alternatives to improve symptoms, among these resources, transcutaneous electrical nerve stimulation (TENS). The aim of this study was to compare the therapeutic and analytical effect of interactive and conventional TENS in high school in PD. The application of TENS, in both groups, was performed on the first day of the menstrual period for 35 minutes. In the interactive TENS all the volunteers chose the following parameters: frequency of 250 Hz, pulse duration of 25 µs and intensity according to sensory level, whether this or the duration of the readjustment of the pulse, every 5 minutes, according to the need for use. In conventional TENS, the following parameters were used: frequency of 100 Hz, pulse duration of 50 µs and intensity according to the previous group. A statistical analysis was performed using the GraphPadPrism® software, version 5.0, being employed Student's test with a significance level of p < 0.05. The result is a reduction in pain among participants in both groups right after treatment. However, there was no difference in the analgesia promoted by the two treatment methods. (AU)

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INTRODUÇÃO: Dismenorreia é a condição dolorosa mais frequente em adolescentes e mulheres jovens causando absenteísmo e presenteísmo no trabalho e na escola. É caracterizada por um quadro álgico leve, moderado ou severo na região pélvica anterior do tipo cólica, o qual pode acontecer antes, durante ou depois do fluxo menstrual. OBJETIVO: Comparar a influência da Estimulação Elétrica Nervosa Transcutânea (TENS) na dor pélvica causada pela dismenorreia primária com os eletrodos aplicados na região pélvica anterior e posterior. MÉTODOS: 50 universitárias foram aleatoriamente distribuídas em dois grupos de 25 voluntárias: Grupo Região Pélvica Anterior (GA) e Grupo Região Pélvica Posterior (GP), que foram submetidas a TENS durante 30 minutos tendo a intensidade aumentada a cada 10 minutos e avaliadas pela Escala Visual Analógica de Dor antes, depois e duas horas após o término do tratamento. As participantes do GA tiveram os eletrodos aplicados na região pélvica anterior e as do GB na região pélvica posterior. RESULTADOS: Houve uma diminuição do quadro álgico nos momentos antes e após o tratamento (GA e GP p<0,0001) e antes e duas horas após o tratamento (GA e GP p<0,0001). Nos momentos depois do tratamento e duas horas após o seu término foi possível observar aumento do quadro álgico no GA (p=1,0000) e diminuição no GP, porém os valores não foram estatisticamente significativos (p=0,8443). CONCLUSÃO: O uso da TENS contribuiu para a redução do quadro álgico das mulheres de ambos os grupos, sem diferença estatística entre estes. Registro Brasileiro de Ensaios Clínicos: RBR-67cjv5.

INTRODUCTION: Dysmenorrhea is the most frequent painful condition in adolescents and young women that causes absenteeism and presenteeism at work and school. It is characterized by a mild, moderate, or severe pain in the anterior pelvic region of the colic type, which can happen before, during, or after menstrual flow. OBJECTIVE: To compare the influence of Transcutaneous Electrical Nerve Stimulation (TENS) in pelvic pain caused by primary dysmenorrhea with the electrodes applied in the anterior and posterior pelvic region. METHODS: 50 university students were randomly assigned to two groups of 25 volunteers: Anterior Pelvic Region Group (GA) and Posterior Pelvic Region Group (GP), who were submitted to TENS for 30 minutes and the intensity increased every 10 minutes and evaluated by the Visual Analog Pain Scale before, after and two hours after the end of treatment. GA participants had the electrodes applied in the anterior pelvic region and GB in the posterior pelvic region. RESULTS: There was a decrease in the pain in the moments before and after treatment (GA and GP p<0.0001) and before and two hours after treatment (GA and GP p <0.0001). In the moments after the treatment and two hours after its end, it was possible to observe an increase in the pain in GA (p=1.0000) and a decrease in the GP, however, the values were not statistically significant (p=0.8443). CONCLUSION: The use of TENS contributed to the reduction of pain in women in both groups, without statistical difference between them. Brazilian Registry of Clinical Trials: RBR-67cjv5.

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ABSTRACT BACKGROUND AND OBJECTIVES Among the main non-pharmacological analgesic techniques are physical therapies such as electrotherapy and cognitive-behavioral techniques, such as hypnosis. The objective of this study was to compare the analgesic effect of transcutaneous electrical nerve stimulation (TENS) and hypnosis in the control of chronic low back pain. METHODS A crossover study that included 19 young adults of both genders with chronic low back pain who underwent TENS and hypnosis, and pain education as a control group. The quality of pain was assessed by the McGill's questionnaire; pain intensity and threshold were assessed by the visual analog scale. The intensity of spontaneous pain, the threshold and intensity of pain induced by cold and the pressure pain threshold before the interventions, immediately after the interventions and 30 minutes after the end of the interventions were evaluated. Statistical analysis was performed with Generalized Mixed Linear Models, with 5% significance, and Cohen's G effect sizes. RESULTS There was a statistically significant decrease in the intensity of spontaneous and cold induced pain in the hypnosis and TENS groups compared to the pain education group. There was a statistically significant reduction of pain in the sensory and evaluation categories in the intervention groups compared to the control group. There was no significant difference for the pressure pain threshold and latency time for cold induced pain. CONCLUSION Hypnosis and TENS decreased the intensity of chronic low back pain with no statistically significant difference between them, but statistically different from the pain education control group.

RESUMO JUSTIFICATIVA E OBJETIVOS Entre as principais técnicas analgésicas não farmacológicas estão as terapias físicas como a eletroterapia e técnicas cognitivo-comportamentais, como a hipnose. O objetivo deste estudo foi comparar o efeito analgésico da estimulação elétrica nervosa transcutânea (TENS) e hipnose no controle da dor lombar crônica. MÉTODOS Estudo do tipo cruzado que incluiu 19 adultos jovens de ambos os sexos portadores de dor lombar crônica, submetidos a TENS, hipnose e educação em dor como grupo controle. A qualidade da dor foi avaliada pelo questionário de McGill, a intensidade e o limiar da dor pela escala analógica visual. Foi avaliada a intensidade da dor espontânea, o limiar e a intensidade de dor ao frio e o limiar da dor à pressão, imediatamente após as intervenções e 30 minutos depois do final das intervenções. A análise estatística foi realizada com modelos lineares generalizados mistos, com 5% de significância, e tamanhos de efeito G de Cohen. RESULTADOS Houve diminuição estatisticamente significativa da intensidade da dor espontânea e ao frio nos grupos hipnose e TENS comparados ao grupo de educação em dor. Ocorreu redução do quadro álgico estatisticamente significativo nas categorias sensorial e avaliativa nos grupos intervenção comparados ao grupo controle. Não houve diferença significativa para o limiar de dor à pressão e o tempo de latência para a dor ao frio. CONCLUSÃO A hipnose e a TENS diminuíram a intensidade da dor lombar crônica sem diferença estatisticamente significativa entre si, porém estatisticamente diferentes em relação ao grupo controle.

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Objective: To compare the segmental and extrasegmental hypoalgesic effects of TENS, IFC and Aussie current on pressure pain threshold (PPT) during and after stimulation in healthy subjects. The second objective was to compare the sensory comfort related to electrical stimulation.Material and Methods: 120 healthy subjects were randomized in TENS, IFC, Aussie current or placebo groups. The electrical stimulation was administered on the forearm. The PPT was measured on the forearm (segmental measure) and on the lower leg (extrasegmental measure) by an algometer at baseline, during and after stimulation of the forearm, and the sensory comfort in relation to electrical stimulation was measured with a visual analogue scale. Statistical analysis was performed using linear mixed models for PPT analysis and one-way ANOVA for sensory comfort analysis.Results: The TENS, IFC and Aussie current increased the segmental and extrasegmental PPTs during application of current compared to the placebo. The PPTs measures and sensory comfort were not significantly different between the TENS, IFC and Aussie current groups.Conclusions: Segmental and extrasegmental hypoalgesic effects may be produced using TENS, IFC or Aussie currents in healthy subjects. Furthermore, all of them presented a similar sensory comfort.

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OBJECTIVE: To compare the effectiveness of tibial nerve transcutaneous electrical nerve stimulation (TENS) for an overactive bladder, considering the sites of application and frequency of attendance. METHODS: This multi-arm randomized controlled trial enrolled 137 adult women (61.0±9.0 years) with overactive bladder from a university hospital. They underwent 12 sessions of 30-min TENS application and were assigned to five groups: one leg, once a week (n=26); one leg, twice a week (n=27); two legs, once a week (n=26); two legs, twice a week (n=28); and placebo (n=30). Symptoms of overactive bladder and its impact on quality of life were evaluated before and after 6 or 12 weeks of treatment using the Overactive Bladder Questionnaire-V8 and voiding diary. ClinicalTrials.gov: NCT01912885. RESULTS: The use of one leg, once a week TENS application reduced the frequency of urgency episodes compared with the placebo (1.0±1.6 vs. 1.4±1.9; p=0.046) and frequency of incontinence episodes compared with the placebo (0.7±1.4 vs.1.4±2.2; p<0.0001). The one-leg, twice a week protocol decreased the urinary frequency compared with the two legs, once a week protocol (8.2±3.5 vs. 9.0±5.1; p=0.026) and placebo (8.2±3.5 vs. 7.9±2.7; p=0.02). Nocturia improved using the two legs, once a week protocol (1.5±1.8) when compared with the one leg, twice a week protocol (1.9±2.0) and placebo (1.7±1.6) (p=0.005 and p=0.027, respectively). Nocturia also improved using the two legs, twice a week protocol when compared with the one leg, twice a week protocol (1.3±1.2 vs.1.9±2.0; p=0.011). CONCLUSION: One-leg stimulation improved the daily urinary frequency, urgency, and incontinence, and the two-leg stimulation once and twice weekly improved nocturia.

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