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Video Game Playing Effects on Obesity in an Adolescent with Autism Spectrum Disorder: A Case Study 电子游戏对自闭症谱系障碍青少年肥胖的影响:个案研究
Pub Date : 2015-12-10 DOI: 10.1155/2015/128365
Brandy E. Strahan, J. Elder
Adolescent obesity has tripled in the past two decades, and adolescents with disabilities, specifically autism spectrum disorders (ASD), may be at greater risk for obesity due to the behavioral, physical, and psychosocial complications related to their disorder. This case study reports the effects of video game playing on an obese adolescent with ASD and illustrates the use of a multiple baseline single subject design. Over 12 weeks, the participant played inactive (6 weeks) and active video games (6 weeks) on the Wii console. Physiological data were evaluated weekly at home. Stress and anxiety were measured via the Stress Survey Schedule for Individuals with Autism and Other Pervasive Non-Developmental Disorders (SSS) and the Behavior Assessment System for Children Second Edition (BASC-2) pre- and postintervention. The Therapy Attitude Inventory (TAI) was used to determine parental perception of video game playing as a socially valid intervention to reduce stress and anxiety. Results demonstrated that active video game playing slowed and/or reduced weight and BMI with minimal changes to waist-to-hip ratios, triceps skinfolds, and stress and anxiety. This study demonstrates how alternative methods for physical activity may be used to improve health outcomes of overweight/obese adolescents with ASD and suggests directions for future research.
青少年肥胖在过去二十年中增加了两倍,残疾青少年,特别是自闭症谱系障碍(ASD),由于与他们的障碍相关的行为、身体和社会心理并发症,可能面临更大的肥胖风险。本案例研究报告了视频游戏对患有自闭症的肥胖青少年的影响,并说明了多基线单受试者设计的使用。在12周的时间里,参与者分别在Wii游戏机上玩非活动(6周)和活动(6周)视频游戏。每周在家评估生理数据。干预前后分别采用《自闭症及其他广泛性非发育障碍患者压力调查表》(SSS)和《儿童行为评估系统第二版》(BASC-2)对压力和焦虑进行测量。使用治疗态度量表(TAI)来确定父母对电子游戏作为一种社会有效干预来减少压力和焦虑的看法。结果表明,积极的电子游戏会减缓或减少体重和BMI,而腰臀比、三头肌皮肤褶皱、压力和焦虑的变化很小。本研究展示了体育活动的替代方法如何用于改善超重/肥胖ASD青少年的健康结果,并为未来的研究提出了方向。
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引用次数: 10
Characteristics of Two-Year College Students on the Autism Spectrum and Their Support Services Experiences 两年制大学生自闭症谱系特征及其支持服务体验
Pub Date : 2015-11-15 DOI: 10.1155/2015/391693
Anne M. Roux, P. Shattuck, Jessica E Rast, Julianna Rava, A. D. Edwards, Xin Wei, Mary McCracken, Jennifer Yu
Approximately 80% of college-going youth with autism in the US attend a 2-year college at some point. These community-based, universally accessible institutions offer both academic and vocational courses and have experience in teaching diverse learners. This study used nationally representative survey data from the National Longitudinal Transition Study-2 to describe the characteristics and services experiences of adults with autism who attended postsecondary education after high school, focusing on those who attended a 2-year college. Over 60% of those who attended 2-year colleges had little to no trouble conversing or performing functional skills like counting change during high school, and extracurricular participation was common (93.8%). Most 2-year college attenders (85.7%) were able to navigate to places outside the home versus 43.9% of those with no postsecondary education. Over half took vocational courses at 2-year colleges, while one-quarter pursued academic study. Less than half (48.6%) of those who disclosed their disability to the school reported receiving services, accommodations, or other help. Most (87.3%) felt they received enough help, but fewer (68.0%) felt the services they received were useful. Future research should delineate specific needs of students with autism in 2-year college settings and identify what supports are needed to improve persistence and completion rates.
在美国,大约80%的自闭症青少年在某种程度上上了两年制大学。这些以社区为基础、可普遍进入的机构提供学术和职业课程,并具有教授不同学习者的经验。本研究使用全国纵向过渡研究-2的全国代表性调查数据来描述高中毕业后接受高等教育的成年自闭症患者的特征和服务体验,重点关注那些上过两年制大学的人。在上过两年制大学的学生中,超过60%的人在高中期间几乎没有遇到交谈或执行功能技能(如计算零钱)的问题,参加课外活动也很常见(93.8%)。大多数两年制大学的学生(85.7%)能够在家庭以外的地方工作,而没有接受过高等教育的学生中这一比例为43.9%。超过一半的人在两年制大学学习职业课程,而四分之一的人继续学术学习。不到一半(48.6%)的学生向学校透露了他们的残疾,他们表示得到了服务、住宿或其他帮助。大多数人(87.3%)认为他们得到了足够的帮助,但较少人(68.0%)认为他们得到的服务是有用的。未来的研究应该描述两年制大学环境中自闭症学生的具体需求,并确定需要哪些支持来提高持久性和完成率。
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引用次数: 43
Parenting Behavior in Mothers of Preschool Children with ASD: Development of a Self-Report Questionnaire 学龄前自闭症儿童母亲的教养行为:自我报告问卷的编制
Pub Date : 2015-10-29 DOI: 10.1155/2015/381236
Greet Lambrechts, J. Maljaars, H. Boonen, Lotte van Esch, K. Van Leeuwen, I. Noens
Parents of young children with autism spectrum disorder (ASD) encounter many daily challenges and often experience much stress. However, little research exists about parenting behavior among these parents. With this study, we aim to address this gap. We examined the structure and internal consistency of a questionnaire intended to measure parenting behavior among mothers of young children with ASD. Furthermore, we compared parenting behavior among mothers of young children with and without ASD between two and six years old. Factor analyses resulted in a factor solution with seven subscales of parenting behavior. Two additional subscales especially relevant for parenting preschoolers with ASD were also considered. Analyses of covariance, controlling for gender and age, showed significantly higher scores for Discipline and Stimulating the Development in the control group in comparison with the ASD group. These findings suggest that mothers of preschoolers with ASD are still trying to find strategies to guide and stimulate their child's behavior and development effectively.
患有自闭症谱系障碍(ASD)的幼儿的父母每天都会遇到许多挑战,经常会经历很大的压力。然而,关于这些父母的育儿行为的研究很少。通过这项研究,我们的目标是解决这一差距。我们检查了一份问卷的结构和内部一致性,该问卷旨在衡量患有自闭症儿童的母亲的养育行为。此外,我们比较了2至6岁之间患有和没有自闭症儿童的母亲的育儿行为。因子分析的结果是一个包含七个养育行为分量表的因子解决方案。还考虑了另外两个特别与养育患有自闭症的学龄前儿童相关的子量表。在控制性别和年龄的情况下,协方差分析显示,与ASD组相比,对照组在纪律和刺激发展方面的得分明显更高。这些发现表明,患有自闭症谱系障碍的学龄前儿童的母亲仍在努力寻找有效指导和刺激孩子行为和发展的策略。
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引用次数: 13
About Face: Evaluating and Managing Tactile Impairment at the Time of Autism Diagnosis 关于脸:自闭症诊断时触觉障碍的评估与处理
Pub Date : 2015-10-28 DOI: 10.1155/2015/612507
Louisa M. T. Silva, Mark Schalock, Kristen R. Gabrielsen
Evaluation for sensory impairment is a routine part of autism diagnosis. Sensory impairment of hearing, vision, or touch results in developmental delay and must be addressed before delay can resolve. Recent studies confirm that tactile impairment is present in autism and can be effectively treated with a tactile stimulation protocol. The research suggests a change in management at the time of autism diagnosis to include evaluation and treatment of tactile impairment. Here we validate screening and management tool for tactile impairment, the Autism Touch and Self-Regulation Checklist, in 404 typical and autistic preschool children. The tool assesses tactile impairment by location and severity. Autistic children were distinguished by mixed pain and numbness on multiple areas including the face and mouth (F = 412.1 (1,402);p < .000). Oral-facial tactile impairment interferes with the tactile stimulus to orienting. We hypothesized that oral-facial tactile impairment and difficulty orienting are predictive of ASD and that severity of tactile impairment is predictive of severity of ASD. Questions evaluating oral-facial and orienting responses correctly predicted 91% of the autism group. Severity of tactile impairment correctly predicted 81% of mild versus severe ASD. Results underscore the importance of evaluating and treating tactile impairment at the time of autism diagnosis.
对感觉障碍的评估是自闭症诊断的常规部分。听觉、视觉或触觉的感觉障碍会导致发育迟缓,必须在发育迟缓得以解决之前加以解决。最近的研究证实,自闭症中存在触觉障碍,可以通过触觉刺激方案有效地治疗。该研究建议在自闭症诊断时改变管理方式,包括对触觉障碍的评估和治疗。在此,我们对404名典型和自闭症学龄前儿童的触觉障碍筛查和管理工具——自闭症触觉和自我调节检查表进行了验证。该工具根据位置和严重程度评估触觉损伤。自闭症儿童以面部和口腔等多部位的混合性疼痛和麻木来区分(F = 412.1 (1,402);p < .000)。口腔-面部触觉障碍干扰定向触觉刺激。我们假设口腔-面部触觉障碍和定向困难可以预测ASD,而触觉障碍的严重程度可以预测ASD的严重程度。评估口腔-面部和定向反应的问题正确预测了91%的自闭症组。触觉损伤的严重程度正确预测了81%的轻度和重度ASD。结果强调了在自闭症诊断时评估和治疗触觉障碍的重要性。
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引用次数: 8
Early Intervention with a Parent-Delivered Massage Protocol Directed at Tactile Abnormalities Decreases Severity of Autism and Improves Child-to-Parent Interactions: A Replication Study. 针对触觉异常的父母提供的按摩方案的早期干预降低了自闭症的严重程度并改善了儿童与父母的互动:一项重复研究。
Pub Date : 2015-01-01 Epub Date: 2015-03-24 DOI: 10.1155/2015/904585
Louisa M T Silva, Mark Schalock, Kristen R Gabrielsen, Sarojini S Budden, Martha Buenrostro, Gretchen Horton

Tactile abnormalities are severe and universal in preschool children with autism. They respond well to treatment with a daily massage protocol directed at tactile abnormalities (QST massage for autism). Treatment is based on a model for autism proposing that tactile impairment poses a barrier to development. Two previous randomized controlled trials evaluating five months of massage treatment reported improvement of behavior, social/communication skills, and tactile and other sensory symptoms. This is the first report from a two-year replication study evaluating the protocol in 103 preschool children with autism. Parents gave daily treatment; trained staff gave weekly treatment and parent support. Five-month outcomes replicated earlier studies and showed normalization of receptive language (18%, P = .03), autistic behavior (32%, P = .006), total sensory abnormalities (38%, P = .0000005), tactile abnormalities (49%, P = .0002), and decreased autism severity (medium to large effect size, P = .008). In addition, parents reported improved child-to-parent interactions, bonding, and decreased parenting stress (44%, P = .00008). Early childhood special education programs are tasked with addressing sensory abnormalities and engaging parents in effective home programs. Until now, they have lacked research-based methods to do so. This program fulfills the need. It is recommended to parents and ECSE programs (ages 3-5) at autism diagnosis.

触觉异常在学龄前自闭症儿童中是严重且普遍的。他们对针对触觉异常的每日按摩治疗反应良好(针对自闭症的QST按摩)。治疗是基于自闭症的一个模型,该模型提出触觉障碍是发展的障碍。先前的两项随机对照试验评估了五个月的按摩治疗,报告了行为、社交/沟通技能、触觉和其他感觉症状的改善。这是一项为期两年的重复研究的第一份报告,该研究对103名学龄前自闭症儿童进行了评估。父母每天给他们治疗;训练有素的工作人员每周提供治疗和家长支持。5个月的结果重复了早期的研究,显示接受性语言正常化(18%,P = .03),自闭症行为正常化(32%,P = .006),感觉异常(38%,P = .0000005),触觉异常(49%,P = .0002),自闭症严重程度降低(中大型效应量,P = .008)。此外,父母报告说,改善了子女与父母的互动、联系,减少了养育压力(44%,P = 0.00008)。早期儿童特殊教育项目的任务是解决感官异常,并让父母参与有效的家庭项目。到目前为止,他们还缺乏基于研究的方法来做到这一点。这个程序满足了需求。在自闭症诊断时推荐给家长和ECSE项目(3-5岁)。
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引用次数: 39
Knowledge of Childhood Autism and Challenges of Management among Medical Doctors in Kaduna State, Northwest Nigeria. 尼日利亚西北部卡杜纳州医生对儿童自闭症的了解和管理挑战。
Pub Date : 2015-01-01 Epub Date: 2015-03-23 DOI: 10.1155/2015/892301
E E Eseigbe, F T Nuhu, T L Sheikh, P Eseigbe, K A Sanni, V O Olisah

Autism is a neurodevelopmental disorder with serious implications in childhood. There is a significant gap in the identification and provision of health and social services for autism in Africa. The knowledge of autism among health care providers and identifying challenges associated with its management could facilitate bridging the gap and ensuring better outcomes. A self-administered tool, the Knowledge about Childhood Autism among Health Workers (KCAHW) questionnaire, was used in assessing knowledge of autism among 175 medical doctors (participants) attending an annual scientific meeting in northwest Nigeria. Other parameters assessed were sociodemographic and professional characteristics of the participants and challenges encountered in the management of autism. Out of 175 questionnaires distributed, 167 (95.4%) were returned. Good knowledge (KCAHW score ≥15) was significantly associated with being a paediatrician or psychiatrist and practicing in a tertiary health facility (P < 0.05), while poor knowledge (KCAHW score <15) was significant among general practitioners (P < 0.05). The highest knowledge gap was associated with onset of autism and its comorbidities (KCAHW Domain 4) while the least was concerning communication impairments (KCAHW Domain 2). Major challenges encountered in autism management were dearth of specialist services, cost of evaluation, and poor caregiver perspectives of autism.

自闭症是一种严重影响儿童的神经发育障碍。非洲在确定和提供针对自闭症的保健和社会服务方面存在重大差距。卫生保健提供者了解自闭症并确定与管理自闭症有关的挑战,可有助于弥合差距并确保取得更好的结果。在尼日利亚西北部参加年度科学会议的175名医生(参与者)中,使用了一种自我管理的工具——卫生工作者关于儿童自闭症的知识调查表。评估的其他参数包括参与者的社会人口学和专业特征,以及在自闭症管理中遇到的挑战。共发放175份问卷,回收167份(95.4%)。良好的知识(KCAHW评分≥15)与成为儿科医生或精神科医生以及在三级卫生机构执业显著相关(P < 0.05),而知识差(KCAHW评分)
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引用次数: 56
Preliminary efficacy of adapted responsive teaching for infants at risk of autism spectrum disorder in a community sample. 在社区样本中,针对自闭症谱系障碍高危婴儿的适应性反应教学的初步效果。
Pub Date : 2015-01-01 Epub Date: 2015-01-11 DOI: 10.1155/2015/386951
Grace T Baranek, Linda R Watson, Lauren Turner-Brown, Samuel H Field, Elizabeth R Crais, Linn Wakeford, Lauren M Little, J Steven Reznick

This study examined the (a) feasibility of enrolling 12-month-olds at risk of ASD from a community sample into a randomized controlled trial, (b) subsequent utilization of community services, and (c) potential of a novel parent-mediated intervention to improve outcomes. The First Year Inventory was used to screen and recruit 12-month-old infants at risk of ASD to compare the effects of 6-9 months of Adapted Responsive Teaching (ART) versus referral to early intervention and monitoring (REIM). Eighteen families were followed for ~20 months. Assessments were conducted before randomization, after treatment, and at 6-month follow-up. Utilization of community services was highest for the REIM group. ART significantly outperformed REIM on parent-reported and observed measures of child receptive language with good linear model fit. Multiphase growth models had better fit for more variables, showing the greatest effects in the active treatment phase, where ART outperformed REIM on parental interactive style (less directive), child sensory responsiveness (less hyporesponsive), and adaptive behavior (increased communication and socialization). This study demonstrates the promise of a parent-mediated intervention for improving developmental outcomes for infants at risk of ASD in a community sample and highlights the utility of earlier identification for access to community services earlier than standard practice.

本研究考察了(a)从社区样本中招募 12 个月大的有 ASD 风险的婴儿参加随机对照试验的可行性,(b)随后社区服务的利用情况,以及(c)新型家长干预措施改善结果的潜力。利用 "一岁量表 "筛选和招募 12 个月大的有 ASD 风险的婴儿,比较 6-9 个月的适应性反应教学 (ART) 与转介到早期干预和监测 (REIM) 的效果。对 18 个家庭进行了约 20 个月的跟踪调查。分别在随机分配前、治疗后和 6 个月的随访中进行了评估。REIM 组对社区服务的利用率最高。在家长报告和观察到的儿童接受语言测量结果方面,ART 的表现明显优于 REIM,且线性模型拟合度较高。多阶段成长模型对更多变量的拟合效果更好,显示出积极治疗阶段的最大效果,在该阶段,ART 在父母互动方式(指令性较少)、儿童感官反应能力(反应不足较少)和适应行为(沟通和社交能力增强)方面的表现优于 REIM。这项研究表明,在社区样本中,以父母为中介的干预措施有望改善有 ASD 风险的婴儿的发育成果,并强调了比标准做法更早地识别并获得社区服务的效用。
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引用次数: 0
Parent-Child Agreement Using the Spence Children's Anxiety Scale and a Thermometer in Children with Autism Spectrum Disorder. 使用Spence儿童焦虑量表和体温计在自闭症谱系障碍儿童中的亲子协议。
Pub Date : 2015-01-01 Epub Date: 2015-04-02 DOI: 10.1155/2015/315495
T May, K Cornish, N J Rinehart

Children with Autism Spectrum Disorder (ASD) experience high anxiety which often prompts clinical referral and requires intervention. This study aimed to compare parent and child reports on the Spence Children's Anxiety Scale (SCAS) and a child-reported "worry thermometer" in 88 children aged 8-13 years, 44 with ASD and 44 age, gender, and perceptual IQ matched typically developing children. There were no gender differences in child report on the SCAS and worry thermometers. Results indicated generally good correlations between parent and child self-reported SCAS symptoms for typically developing children but poor agreement in parent-child ASD dyads. The worry thermometer child-report did not reflect child or parent reports on the SCAS. Findings suggest 8-13-year-old children with ASD may have difficulties accurately reporting their anxiety levels. The clinical implications were discussed.

患有自闭症谱系障碍(ASD)的儿童经历高度焦虑,这往往促使临床转诊并需要干预。本研究旨在比较88名8-13岁儿童的斯宾塞儿童焦虑量表(SCAS)和儿童报告的“焦虑温度计”,其中44名患有ASD, 44名年龄、性别和感知智商匹配的正常发育儿童。儿童对SCAS和焦虑体温计的报告无性别差异。结果表明,在典型发育儿童中,父母和孩子自我报告的SCAS症状之间普遍存在良好的相关性,但在父母和孩子之间的一致性较差。忧虑温度计儿童报告并没有反映儿童或家长对SCAS的报告。研究结果表明,8-13岁的自闭症儿童可能很难准确地报告他们的焦虑水平。讨论了临床意义。
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引用次数: 16
Gait deviations in children with autism spectrum disorders: a review. 自闭症谱系障碍儿童的步态偏差:综述。
Pub Date : 2015-01-01 Epub Date: 2015-04-02 DOI: 10.1155/2015/741480
Deirdre Kindregan, Louise Gallagher, John Gormley

In recent years, it has become clear that children with autism spectrum disorders (ASDs) have difficulty with gross motor function and coordination, factors which influence gait. Knowledge of gait abnormalities may be useful for assessment and treatment planning. This paper reviews the literature assessing gait deviations in children with ASD. Five online databases were searched using keywords "gait" and "autism," and 11 studies were found which examined gait in childhood ASD. Children with ASD tend to augment their walking stability with a reduced stride length, increased step width and therefore wider base of support, and increased time in the stance phase. Children with ASD have reduced range of motion at the ankle and knee during gait, with increased hip flexion. Decreased peak hip flexor and ankle plantar flexor moments in children with ASD may imply weakness around these joints, which is further exhibited by a reduction in ground reaction forces at toe-off in children with ASD. Children with ASD have altered gait patterns to healthy controls, widened base of support, and reduced range of motion. Several studies refer to cerebellar and basal ganglia involvement as the patterns described suggest alterations in those areas of the brain. Further research should compare children with ASD to other clinical groups to improve assessment and treatment planning.

近年来,自闭症谱系障碍(asd)儿童在大运动功能和协调方面存在困难,这是影响步态的因素。步态异常的知识可能有助于评估和治疗计划。本文综述了评估ASD儿童步态偏差的文献。以“步态”和“自闭症”为关键词搜索了5个在线数据库,发现了11项关于儿童ASD步态的研究。ASD患儿倾向于通过减小步长、增大步宽从而扩大支撑基础和增加站立阶段的时间来增强其行走稳定性。患有ASD的儿童在走路时踝关节和膝关节的活动范围减小,髋部屈曲增加。ASD患儿髋屈肌和足底屈肌峰值力矩的减少可能意味着这些关节周围的无力,这进一步表现为ASD患儿脚尖起跳时地面反作用力的减少。与健康对照相比,自闭症儿童的步态模式发生了改变,支撑基础变宽,活动范围减小。一些研究提到小脑和基底神经节受累,因为所描述的模式表明大脑的这些区域发生了变化。进一步的研究应该将自闭症儿童与其他临床组进行比较,以改进评估和治疗计划。
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引用次数: 111
Gaze Behavior of Children with ASD toward Pictures of Facial Expressions. ASD儿童对面部表情图片的注视行为
Pub Date : 2015-01-01 Epub Date: 2015-05-19 DOI: 10.1155/2015/617190
Soichiro Matsuda, Yasuyo Minagawa, Junichi Yamamoto

Atypical gaze behavior in response to a face has been well documented in individuals with autism spectrum disorders (ASDs). Children with ASD appear to differ from typically developing (TD) children in gaze behavior for spoken and dynamic face stimuli but not for nonspeaking, static face stimuli. Furthermore, children with ASD and TD children show a difference in their gaze behavior for certain expressions. However, few studies have examined the relationship between autism severity and gaze behavior toward certain facial expressions. The present study replicated and extended previous studies by examining gaze behavior towards pictures of facial expressions. We presented ASD and TD children with pictures of surprised, happy, neutral, angry, and sad facial expressions. Autism severity was assessed using the Childhood Autism Rating Scale (CARS). The results showed that there was no group difference in gaze behavior when looking at pictures of facial expressions. Conversely, the children with ASD who had more severe autistic symptomatology had a tendency to gaze at angry facial expressions for a shorter duration in comparison to other facial expressions. These findings suggest that autism severity should be considered when examining atypical responses to certain facial expressions.

在自闭症谱系障碍(asd)患者中,对面部的非典型凝视行为已经得到了很好的记录。ASD儿童在言语和动态面部刺激下的凝视行为与正常发育(TD)儿童不同,而在非言语、静态面部刺激下则不同。此外,ASD儿童和TD儿童在某些表情的注视行为上表现出差异。然而,很少有研究调查自闭症严重程度与注视某些面部表情行为之间的关系。本研究复制并扩展了之前的研究,研究了人们对面部表情图片的凝视行为。我们向ASD和TD儿童展示了惊讶、快乐、中性、愤怒和悲伤的面部表情图片。使用儿童自闭症评定量表(CARS)评估自闭症严重程度。结果表明,在观看面部表情图片时,注视行为没有组间差异。相反,与其他面部表情相比,自闭症症状更严重的自闭症儿童倾向于盯着愤怒的面部表情看的时间更短。这些发现表明,在检查对某些面部表情的非典型反应时,应该考虑自闭症的严重程度。
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引用次数: 27
期刊
Autism Research and Treatment
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