Effect of a Multimodal Pain Therapy Concept Including Intensive Physiotherapy on the Perception of Pain and the Quality of Life of Patients With Chronic Back Pain: A Prospective Observational Multicenter Study Named "RütmuS".

IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY
Pain Research & Management Pub Date : 2025-05-10 eCollection Date: 2025-01-01 DOI:10.1155/prm/6693678
Katharina Zaglauer, Andrea Kunsorg, Vanessa Jakob, Lara Görg, Arndt Oehlschlägel, Rainer Riedel, Ursula Marschall, Dieter Welsink, Horst Schuhmacher, Maria Wittmann
{"title":"Effect of a Multimodal Pain Therapy Concept Including Intensive Physiotherapy on the Perception of Pain and the Quality of Life of Patients With Chronic Back Pain: A Prospective Observational Multicenter Study Named \"RütmuS\".","authors":"Katharina Zaglauer, Andrea Kunsorg, Vanessa Jakob, Lara Görg, Arndt Oehlschlägel, Rainer Riedel, Ursula Marschall, Dieter Welsink, Horst Schuhmacher, Maria Wittmann","doi":"10.1155/prm/6693678","DOIUrl":null,"url":null,"abstract":"<p><p><b>Question and Outcome Measures:</b> In this study, an intervention group (multimodal therapy for chronic back pain) and a control group (standard outpatient treatment) were compared with regard to the primary endpoint of pain (NRS) at rest and the secondary endpoints pain (NRS) during movement, general health status (Short Form 12 (SF-12)), health-related quality of life (EQ-5D-5L), pain disability index (PDI), Hospital Anxiety and Depression Scale-Germany (HADS-D), and Hannover Functional Ability Questionnaire for Measuring Back Pain-Related Disability (FFbH-R). <b>Design and Participants:</b> The total patient cohort of this prospective observational multicenter study consisted of 477 patients who were initially enrolled in the study from January 2019 to September 2020. <b>Intervention:</b> The intervention group received physiotherapy, pain therapy (pain-therapeutic, body-related, and patient-specific treatment), and control examinations from the responsible physician in a 6-month structured interdisciplinary program. The evaluation points used in the analysis are the baseline survey, 6 months and 12 months after the start of the study. <b>Results:</b> A total of 477 patients (243 in the intervention group and 234 in the control group) were included in the analysis; 42 patients in the intervention group deviated from the eligibility criteria due to insufficient adherence to study participation. Nonetheless, they were included in the analysis in line with the ITT principle. The primary endpoint, pain at rest (NRS), showed greater reductions in the intervention group compared to the control group, with mean differences of -0.492 (95% CI: [-0.866, -0.118], <i>p</i> = 0.010) at 6 months (EVA 3) and -0.463 (95% CI: [-0.837, -0.089], <i>p</i> = 0.015) at 12 months (EVA 5), respectively. Regarding the secondary endpoints, pain during movement exhibited a significantly greater reduction in the intervention group compared to the control group (<i>p</i> < 0.001). Quality of life, measured via the EQ-5D-5L index, improved significantly more in the intervention group than in the control group, as did functional capacity (FFbH-R) and physical health (SF-12 KSK) (<i>p</i> < 0.001). In contrast, mental health (SF-12 PSK) declined significantly during the intervention (<i>p</i> < 0.001). Disability (PDI) exhibited a significantly greater reduction in the intervention group compared to the control group (<i>p</i> < 0.001), whereas anxiety and depression levels (HADS-D) showed only slight changes in both groups, with anxiety being significant at <i>p</i> = 0.0164 and depression not significant at <i>p</i> = 0.1093. These results underscore the intervention's effectiveness across multiple health dimensions, particularly pain reduction and quality of life. <b>Conclusion:</b> Multimodal pain therapy over a 6-month period is an effective intervention to improve the perception of pain at rest and during movement while enhancing the subjective quality of life. These benefits persist beyond the therapy period, underscoring the intervention's lasting impact. <b>Trial Registration:</b> German Clinical Trials Register: DRKS00015800.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2025 ","pages":"6693678"},"PeriodicalIF":2.5000,"publicationDate":"2025-05-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12085246/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pain Research & Management","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1155/prm/6693678","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Question and Outcome Measures: In this study, an intervention group (multimodal therapy for chronic back pain) and a control group (standard outpatient treatment) were compared with regard to the primary endpoint of pain (NRS) at rest and the secondary endpoints pain (NRS) during movement, general health status (Short Form 12 (SF-12)), health-related quality of life (EQ-5D-5L), pain disability index (PDI), Hospital Anxiety and Depression Scale-Germany (HADS-D), and Hannover Functional Ability Questionnaire for Measuring Back Pain-Related Disability (FFbH-R). Design and Participants: The total patient cohort of this prospective observational multicenter study consisted of 477 patients who were initially enrolled in the study from January 2019 to September 2020. Intervention: The intervention group received physiotherapy, pain therapy (pain-therapeutic, body-related, and patient-specific treatment), and control examinations from the responsible physician in a 6-month structured interdisciplinary program. The evaluation points used in the analysis are the baseline survey, 6 months and 12 months after the start of the study. Results: A total of 477 patients (243 in the intervention group and 234 in the control group) were included in the analysis; 42 patients in the intervention group deviated from the eligibility criteria due to insufficient adherence to study participation. Nonetheless, they were included in the analysis in line with the ITT principle. The primary endpoint, pain at rest (NRS), showed greater reductions in the intervention group compared to the control group, with mean differences of -0.492 (95% CI: [-0.866, -0.118], p = 0.010) at 6 months (EVA 3) and -0.463 (95% CI: [-0.837, -0.089], p = 0.015) at 12 months (EVA 5), respectively. Regarding the secondary endpoints, pain during movement exhibited a significantly greater reduction in the intervention group compared to the control group (p < 0.001). Quality of life, measured via the EQ-5D-5L index, improved significantly more in the intervention group than in the control group, as did functional capacity (FFbH-R) and physical health (SF-12 KSK) (p < 0.001). In contrast, mental health (SF-12 PSK) declined significantly during the intervention (p < 0.001). Disability (PDI) exhibited a significantly greater reduction in the intervention group compared to the control group (p < 0.001), whereas anxiety and depression levels (HADS-D) showed only slight changes in both groups, with anxiety being significant at p = 0.0164 and depression not significant at p = 0.1093. These results underscore the intervention's effectiveness across multiple health dimensions, particularly pain reduction and quality of life. Conclusion: Multimodal pain therapy over a 6-month period is an effective intervention to improve the perception of pain at rest and during movement while enhancing the subjective quality of life. These benefits persist beyond the therapy period, underscoring the intervention's lasting impact. Trial Registration: German Clinical Trials Register: DRKS00015800.

包括强化物理治疗在内的多模式疼痛治疗概念对慢性背痛患者疼痛感知和生活质量的影响:一项名为“r tmus”的前瞻性观察性多中心研究。
问题和结果测量:在本研究中,对干预组(多模式治疗慢性背痛)和对照组(标准门诊治疗)在休息时疼痛的主要终点(NRS)和运动时疼痛的次要终点(NRS)、一般健康状况(SF-12)、健康相关生活质量(EQ-5D-5L)、疼痛残疾指数(PDI)、医院焦虑和抑郁量表-德国(HADS-D)、汉诺威背痛相关残疾功能能力问卷(FFbH-R)。设计和参与者:这项前瞻性观察性多中心研究的总患者队列包括477名患者,这些患者最初于2019年1月至2020年9月入组。干预:干预组接受物理治疗、疼痛治疗(疼痛治疗、身体相关治疗和患者特异性治疗),并由负责医生进行为期6个月的结构化跨学科项目的对照检查。分析中使用的评价点是基线调查、研究开始后6个月和12个月。结果:共纳入477例患者(干预组243例,对照组234例);干预组中有42例患者因参与研究的依从性不足而偏离了入选标准。尽管如此,它们还是按照国际电话咨询公司的原则列入了分析。主要终点,静止疼痛(NRS),干预组与对照组相比,在6个月(EVA 3)时的平均差异为-0.492 (95% CI: [-0.866, -0.118], p = 0.010),在12个月(EVA 5)时的平均差异为-0.463 (95% CI: [-0.837, -0.089], p = 0.015)。至于次要终点,与对照组相比,干预组在运动过程中的疼痛明显减少(p < 0.001)。通过EQ-5D-5L指数测量的生活质量,干预组的改善明显大于对照组,功能能力(FFbH-R)和身体健康(SF-12 KSK)的改善也明显大于对照组(p < 0.001)。相比之下,心理健康(SF-12 PSK)在干预期间显著下降(p < 0.001)。与对照组相比,干预组的残疾(PDI)显著降低(p < 0.001),而两组的焦虑和抑郁水平(HADS-D)仅略有变化,焦虑显著(p = 0.0164),抑郁无显著(p = 0.1093)。这些结果强调了干预措施在多个健康方面的有效性,特别是减轻疼痛和提高生活质量。结论:为期6个月的多模式疼痛治疗是一种有效的干预措施,可以改善休息和运动时的疼痛感觉,同时提高主观生活质量。这些益处持续超过治疗期,强调了干预的持久影响。试验注册:德国临床试验注册:DRKS00015800。
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
Pain Research & Management
Pain Research & Management CLINICAL NEUROLOGY-
CiteScore
5.30
自引率
0.00%
发文量
109
审稿时长
>12 weeks
期刊介绍: Pain Research and Management is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies in all areas of pain management. The most recent Impact Factor for Pain Research and Management is 1.685 according to the 2015 Journal Citation Reports released by Thomson Reuters in 2016.
×
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:481959085
Book学术官方微信