Effectiveness of a Person-Centered Interdisciplinary Rehabilitation Treatment of Post-COVID-19 Condition: Protocol for a Single-Case Experimental Design Study.

IF 1.4 Q3 HEALTH CARE SCIENCES & SERVICES JMIR Research Protocols Pub Date : 2024-10-11 DOI:10.2196/63951
Carolina M H Wiertz, Thijs van Meulenbroek, Cynthia Lamper, Bea Hemmen, Simone Sep, Ivan Huijnen, Marielle E J B Goossens, Jako Burgers, Jeanine Verbunt
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Abstract

Background: Patients with post-COVID-19 condition (PCC) experience a wide range of complaints (physical, cognitive, and mental), sometimes with high levels of disability in daily activities. Evidence of effective interdisciplinary rehabilitation treatment is lacking. A person-centered, biopsychosocial, interdisciplinary rehabilitation program, adapted to expert opinions and the patient's needs, was therefore developed.

Objective: This study aims to present a study protocol for a clinical trial to evaluate the effect of a new, person-centered, interdisciplinary rehabilitation treatment for PCC. It is aimed at improving participation in society and health-related quality of life in patients with PCC who perceive a high level of disability in daily activities or participation.

Methods: A total of 20 Dutch adults, aged 18 years or older, with high levels of disability in daily activities and participation in society will be included in this replicated and randomized single-case experimental design study, from October 2023 onward. The replicated and randomized single-case experimental design consists of 3 phases. The baseline phase is the observational period, in which no specific treatment will be given. In the intervention phase, patients will receive the new outpatient treatment 3 times a week for 12 weeks, followed by a 12-week follow-up phase. During the intervention phase, the treatment will be personalized according to the patient's physical, mental, and cognitive symptoms and goals. The treatment team can consist of a rehabilitation physician, physiotherapist, occupational therapist, speech therapist, and psychologist. The primary outcomes of the study are daily diaries, which consist of 8 questions selected from validated questionnaires (Utrecht Scale for Evaluation of Rehabilitation-Participation, EQ-5D-5L, and the Hospital Anxiety and Depression Scale). The other primary outcome measurements are participation in society (Utrecht Scale for Evaluation of Rehabilitation-Participation) and health-related quality of life (EQ-5D-5L). The secondary outcomes are physical tests and validated questionnaires aimed at physical, mental, and cognitive complaints. Effect evaluation based on daily assessments will include visual analysis, calculation of effect sizes (Nonoverlap of All Pairs), randomization tests, and multilevel analysis. In addition, other analyses will be based on ANOVA or a 2-tailed Student t test.

Results: Data collection for this study started in October 2023 and is planned to be completed in July 2024. The results will be published in peer-reviewed journals and presented at international conferences.

Conclusions: This is the first study investigating the effect of an interdisciplinary rehabilitation treatment with a person-centered, biopsychosocial approach in patients with PCC. Our findings will help to improve the treatment and support of patients with PCC.

Trial registration: German Clinical Trials Register DRKS00032636; https://drks.de/search/en/trial/DRKS00032636.

International registered report identifier (irrid): DERR1-10.2196/63951.

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以人为本的跨学科康复治疗对后 COVID-19 症状的疗效:单病例实验设计研究方案。
背景:COVID-19 后遗症(PCC)患者会出现各种不适(身体、认知和精神方面),有时在日常活动中会出现高度残疾。目前缺乏有效的跨学科康复治疗证据。因此,我们根据专家的意见和患者的需求,制定了一项以人为本的生物心理社会跨学科康复计划:本研究旨在介绍一项临床试验的研究方案,以评估以人为本、跨学科的新型 PCC 康复治疗的效果。目的:本研究旨在介绍一项临床试验的研究方案,以评估一种以人为本、跨学科的新型 PCC 康复治疗方法的效果,其目的是改善 PCC 患者的社会参与和与健康相关的生活质量,因为这些患者认为自己在日常活动或参与方面存在严重残疾:从 2023 年 10 月起,共有 20 名年龄在 18 岁或以上、在日常活动和社会参与方面有高度残疾的荷兰成年人将被纳入这项复制和随机单病例实验设计研究。复制和随机单一病例实验设计包括三个阶段。基线阶段为观察期,在此期间不进行任何具体治疗。在干预阶段,患者将接受新的门诊治疗,每周 3 次,为期 12 周,然后是为期 12 周的随访阶段。在干预阶段,将根据患者的身体、精神和认知症状及目标进行个性化治疗。治疗团队可由康复医师、物理治疗师、职业治疗师、语言治疗师和心理学家组成。研究的主要结果是每日日记,其中包括从有效问卷(乌得勒支康复参与评估量表、EQ-5D-5L 和医院焦虑抑郁量表)中选出的 8 个问题。其他主要测量结果包括社会参与度(乌得勒支康复参与度评估量表)和与健康相关的生活质量(EQ-5D-5L)。次要结果是身体测试和针对身体、精神和认知症状的有效问卷。基于日常评估的效果评估将包括视觉分析、效果大小计算(所有配对的非重叠)、随机化测试和多层次分析。此外,其他分析将基于方差分析或双尾学生 t 检验:本研究的数据收集工作于 2023 年 10 月开始,计划于 2024 年 7 月完成。研究结果将在同行评审期刊上发表,并在国际会议上展示:这是第一项调查跨学科康复治疗效果的研究,该治疗采用以人为本的生物心理社会方法,适用于 PCC 患者。我们的研究结果将有助于改善对 PCC 患者的治疗和支持:德国临床试验注册中心 DRKS00032636;https://drks.de/search/en/trial/DRKS00032636.International 注册报告标识符 (irrid):DERR1-10.2196/63951。
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CiteScore
2.40
自引率
5.90%
发文量
414
审稿时长
12 weeks
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