首页> 外文期刊>Journal of Neurology, Neurosurgery and Psychiatry >A pragmatic parallel arm multi-centre randomised controlled trial to assess the effectiveness and cost-effectiveness of a group-based fatigue management programme (FACETS) for people with multiple sclerosis
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A pragmatic parallel arm multi-centre randomised controlled trial to assess the effectiveness and cost-effectiveness of a group-based fatigue management programme (FACETS) for people with multiple sclerosis

机译:务实的多臂平行多中心随机对照试验,用于评估针对多发性硬化症患者的基于小组的疲劳管理计划(FACETS)的有效性和成本效益

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Background Fatigue is a common and troubling symptom for people with multiple sclerosis (MS). Aim To evaluate the effectiveness and cost-effectiveness of a six-session group-based programme for managing MS-fatigue (Fatigue: Applying Cognitive behavioural and Energy effectiveness Techniques to lifeStyle (FACETS)). Methods Three-centre parallel arm randomised controlled trial with economic evaluation. Patients with MS and significant fatigue were randomised to FACETS plus current local practice (FACETS) or current local practice alone (CLP), using concealed computergenerated randomisation. Participant blinding was not possible. Primary outcomes were fatigue severity (Fatigue Assessment Instrument), self-efficacy (Multiple Sclerosis- Fatigue Self-Efficacy) and disease-specific quality of life (Multiple Sclerosis Impact Scale (MSIS-29)) at 1 and 4 months postintervention (follow-up 1 and 2). Quality adjusted life years (QALYs) were calculated (EuroQoL 5- Dimensions questionnaire and the Short-form 6- Dimensions questionnaire). Results Between May 2008 and November 2009, 164 patients were randomised; primary outcome data were available for 146 (89%). Statistically significant differences favour the intervention group on fatigue selfefficacy at follow-up 1 (mean difference (MD) 9, 95% CI (4 to 14), standardised effect size (SES) 0.54, p=0.001) and follow-up 2 (MD 6, 95% CI (0 to 12), SES 0.36, p=0.05) and fatigue severity at follow-up 2 (MD -0.36, 95% CI (-0.63 to -0.08), SES -0.35, p=0.01) but no differences for MSIS-29 or QALYs. No adverse events reported. Estimated cost per person for FACETS is £453; findings suggest an incremental cost-effectiveness ratio of £2157 per additional person with a clinically significant improvement in fatigue. Conclusions FACETS is effective in reducing fatigue severity and increasing fatigue self-efficacy. However, it is difficult to assess the additional cost in terms of costeffectiveness (ie, cost per QALY) as improvements in fatigue are not reflected in the QALY outcomes, with no significant differences between FACETS and CLP. The strengths of this trial are its pragmatic nature and high external validity.
机译:背景疲劳是多发性硬化症(MS)患者的常见症状和令人不安的症状。目的评估六阶段基于小组的管理MS疲劳(疲劳:将认知行为和能量效率技术应用于生活方式(FACETS))的有效性和成本效益。方法采用经济评价的三中心平行臂随机对照试验。患有MS和严重疲劳的患者使用隐蔽的计算机生成的随机方法,随机分为FACETS加当前局部治疗(FACETS)或仅当前局部治疗(CLP)。参与者盲目化是不可能的。主要结局指标为干预后1和4个月的疲劳严重程度(疲劳评估工具),自我效能(多发性硬化症-疲劳自我效能)和特定疾病的生活质量(多发性硬化症影响量表(MSIS-29))( 1和2)。计算质量调整生命年(QALYs)(EuroQoL 5维问卷和简表6维问卷)。结果2008年5月至2009年11月,随机抽取164例患者。主要结果数据为146(89%)。统计学上的显着差异有利于干预组在随访1(平均差异(MD)9、95%CI(4至14),标准化效应量(SES)0.54,p = 0.001)和随访2(干预后) MD 6,95%CI(0至12),SES 0.36,p = 0.05)和随访2时的疲劳严重程度(MD -0.36,95%CI(-0.63至-0.08),SES -0.35,p = 0.01 ),但对于MSIS-29或QALY则没有区别。没有不良反应的报道。 FACETS的每人估计费用为453英镑;研究结果表明,每增加一个人,其成本效益比将增加2157英镑,并且在疲劳方面具有明显的临床改善。结论FACETS可有效减轻疲劳严重程度并提高疲劳自我效能。但是,由于疲劳改善并未反映在QALY结果中,因此FACETS和CLP之间没有显着差异,因此很难从成本效益(即每QALY成本)方面评估额外成本。该试验的优势在于其务实的性质和高度的外部有效性。

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