在线多组件程序(FATIGUEWALK)对慢性疲劳综合征的疗效:随机对照试验

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-04-01 Epub Date: 2023-12-21 DOI:10.1037/hea0001346
Mayte Serrat, Jaime Navarrete, Sònia Ferrés, William Auer, Ramon Sanmartín-Sentañes, Rubén Nieto, Randy Neblett, Xavier Borràs, Juan V Luciano, Albert Feliu-Soler
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引用次数: 0

摘要

研究目的本研究旨在评估名为 "FATIGUEWALK"(FaW)的在线多成分干预与常规治疗(TAU)相比,对慢性疲劳综合征/肌痛性脑脊髓炎(CFS/ME)患者的疗效:方法:FaW包括疼痛神经科学教育、治疗性运动、认知重组和正念训练。共有 428 名 CFS/ME 患者被随机分为两个研究组:在线 FaW 加 TAU 与单独 TAU。该研究是一项单盲随机对照试验。在为期12周的FaW干预后,对患者报告的疲劳、疼痛、焦虑、抑郁和身体功能等结果进行了验证:在疲劳的多维方面(Cohen's d 从 0.25 到 0.73 不等)和大多数次要结果(疼痛和疲劳强度、抑郁和焦虑症状、功能障碍、运动恐惧、身体功能)方面,观察到在线 FaW 与单独 TAU 相比有统计学意义的改善(中小规模效应)。FaW与TAU相比,绝对风险降低了19%,95%置信区间(CI)[12.19, 25.80],治疗所需人数=6,95%CI[3.9, 8.2]。总体而言,在包括无纤维肌痛合并症患者(n = 70)的敏感性分析中也观察到了类似的临床改善:这是第一项评估在TAU基础上添加在线多成分干预的短期疗效的研究,与单独使用TAU相比,对CFS/ME的治疗效果更好。有必要进行更多试验,包括治疗剂量相当的积极对照组,并评估在线FaW的长期有效性。(PsycInfo Database Record (c) 2023 APA, 版权所有)。
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Effectiveness of an online multicomponent program (FATIGUEWALK) for chronic fatigue syndrome: A randomized controlled trial.

Objective: This study aimed to evaluate the effectiveness of an online multicomponent intervention called FATIGUEWALK (FaW) compared to treatment as usual (TAU) in patients with chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME).

Method: FaW included pain neuroscience education, therapeutic exercise, cognitive restructuring, and mindfulness training. A total of 428 patients with CFS/ME were randomized into two study arms: online FaW plus TAU versus TAU alone. A single-blinded randomized controlled trial was conducted. Validated patient-reported outcome measures of fatigue, pain, anxiety, depression, and physical function were collected at baseline and posttreatment, following the FaW intervention, which lasted 12 weeks.

Results: Statistically significant improvements (with small-to-moderate effect sizes) were observed in online FaW versus TAU alone with respect to multidimensional aspects of fatigue (Cohen's d ranging from 0.25 to 0.73) and most secondary outcomes (pain and fatigue intensity, depressive and anxious symptomatology, functional impairment, kinesiophobia, physical functioning). The absolute risk reduction in FaW versus TAU was 19%, 95% confidence interval (CI) [12.19, 25.80] with number needed to treat = 6, 95% CI [3.9, 8.2]. Overall, similar clinical improvements were observed in sensitivity analyses including a subgroup of patients without comorbidity with fibromyalgia (n = 70).

Conclusions: This is the first study to assess the short-term effectiveness of an online multicomponent intervention added to TAU, compared to TAU alone, for the management of CFS/ME. Further trials, including active control groups with an equivalent treatment dose, and assessing the long-term effectiveness of the online FaW, are warranted. (PsycInfo Database Record (c) 2024 APA, all rights reserved).

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