It is time for using adequate assessment and new designs to improve the effectiveness of treatment in chronic musculoskeletal pain

R. Smeets
{"title":"It is time for using adequate assessment and new designs to improve the effectiveness of treatment in chronic musculoskeletal pain","authors":"R. Smeets","doi":"10.3109/21679169.2013.862909","DOIUrl":null,"url":null,"abstract":"’ t know who benefi ts most from what type of treatment – or sometimes even combining types of CBT that might also be contra productive, for example gradually increasing activities by using operant principles on a time contingent basis and teaching the patient to rebalance activity – rest using a pain-contingent approach. Results of randomized, controlled trials (RCTs) in which multidisciplinary treatments are being studied show only low to moderate effect sizes and at least half of the patients do not even show a clinically relevant improvement of personal relevant activities and participation (6). It should be mentioned that many trials do not even use personal relevant outcome measures. But why are the results so moderate? Shouldn ’ t we fi rst perform an adequate assessment of each patient on the basis of his/her goals and a hierarchy of factors that maintain the chronicity of disability to decide what treatment modalities should be provided? I do think that is what we commonly do in clinical practice, but it is diffi cult to study within an RCT design (7). By applying newer techniques using sophisticated statistical analyses, such as randomization testing in single case design (SCD) studies (8), we can make signifi cant progress. This type of study really resembles our daily clinical practice, and by multiple sampling of each patient provides much data to ensure suffi cient power to test whether the hypothesis that the selected treatment modality works can be confi rmed or rejected. Unfortunately, most journals, and especially communities involved in meta-analysis such as the Cochrane collaboration, still view this type of study as being of low quality. I do think it is time to change this view. Another important topic of intervention studies is the description of the content of the treatment and the check as to whether the provided treatment is similar to the treatment protocol, the so-called process evaluation. Many studies still only briefl y discuss the content and treatment rationale (underlying theory) and hardly ever present data on the process evaluation. Regrettably, an extensive description of the diagnostic process, selection of treatment and EDITORIAL","PeriodicalId":186472,"journal":{"name":"The European Journal of Physiotherapy","volume":"52 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2013-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The European Journal of Physiotherapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/21679169.2013.862909","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

’ t know who benefi ts most from what type of treatment – or sometimes even combining types of CBT that might also be contra productive, for example gradually increasing activities by using operant principles on a time contingent basis and teaching the patient to rebalance activity – rest using a pain-contingent approach. Results of randomized, controlled trials (RCTs) in which multidisciplinary treatments are being studied show only low to moderate effect sizes and at least half of the patients do not even show a clinically relevant improvement of personal relevant activities and participation (6). It should be mentioned that many trials do not even use personal relevant outcome measures. But why are the results so moderate? Shouldn ’ t we fi rst perform an adequate assessment of each patient on the basis of his/her goals and a hierarchy of factors that maintain the chronicity of disability to decide what treatment modalities should be provided? I do think that is what we commonly do in clinical practice, but it is diffi cult to study within an RCT design (7). By applying newer techniques using sophisticated statistical analyses, such as randomization testing in single case design (SCD) studies (8), we can make signifi cant progress. This type of study really resembles our daily clinical practice, and by multiple sampling of each patient provides much data to ensure suffi cient power to test whether the hypothesis that the selected treatment modality works can be confi rmed or rejected. Unfortunately, most journals, and especially communities involved in meta-analysis such as the Cochrane collaboration, still view this type of study as being of low quality. I do think it is time to change this view. Another important topic of intervention studies is the description of the content of the treatment and the check as to whether the provided treatment is similar to the treatment protocol, the so-called process evaluation. Many studies still only briefl y discuss the content and treatment rationale (underlying theory) and hardly ever present data on the process evaluation. Regrettably, an extensive description of the diagnostic process, selection of treatment and EDITORIAL
是时候使用适当的评估和新的设计,以提高治疗慢性肌肉骨骼疼痛的有效性
我不知道谁从哪种治疗中获益最多——或者有时甚至结合不同类型的认知行为治疗,这也可能适得其反,例如,通过在时间偶然的基础上使用操作原则逐渐增加活动,并教患者重新平衡活动——使用疼痛偶然的方法休息。研究多学科治疗的随机对照试验(RCTs)的结果显示,只有低到中等的效应量,至少一半的患者甚至没有表现出个人相关活动和参与的临床相关改善(6)。应该提到的是,许多试验甚至没有使用个人相关的结局指标。但为什么结果如此温和呢?难道我们不应该首先对每个病人进行充分的评估,根据他/她的目标和维持残疾慢性的因素层次来决定应该提供什么样的治疗方式吗?我确实认为这是我们在临床实践中通常做的事情,但很难在RCT设计中进行研究(7)。通过应用使用复杂统计分析的新技术,例如单例设计(SCD)研究中的随机化测试(8),我们可以取得重大进展。这种类型的研究非常类似于我们的日常临床实践,通过对每个患者进行多次抽样,提供了大量的数据,以确保有足够的能力来检验所选择的治疗方式有效的假设是否可以被证实或拒绝。不幸的是,大多数期刊,特别是参与meta分析的社区,如Cochrane合作,仍然认为这类研究的质量很低。我认为是时候改变这种观点了。干预研究的另一个重要课题是描述治疗的内容,并检查所提供的治疗是否与治疗方案相似,即所谓的过程评估。许多研究仍然只是简单地讨论了治疗的内容和基本原理(基础理论),几乎没有提供有关过程评估的数据。遗憾的是,广泛的描述诊断过程,选择治疗和编辑
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书