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针对患有慢性健康状况的青少年的混合疗法以提高与疲劳相关的自我效能(强化治疗):一项单病例多基线研究方案

Blended therapy for adolescents with chronic health conditions to increase fatigue-related self-efficacy (Booster): protocol for a single-case multiple baseline study.

作者信息

Stutvoet Maartje D, Vroegindeweij Anouk, Houtveen Jan, van Litsenburg Raphaële R L, van de Putte Elise, Veltkamp Remco C, Nijhof Sanne L

机构信息

Department of Paediatrics, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.

Princess Máxima Centre for Paediatric Oncology, Utrecht, The Netherlands.

出版信息

Trials. 2025 Jul 24;26(1):255. doi: 10.1186/s13063-025-08960-1.

Abstract

BACKGROUND

Fatigue is a common symptom in adolescents with a chronic health condition. Persistent fatigue and its impairments may be prevented by early intervention with Booster. Booster is a transdiagnostic blended care intervention that aims to increase fatigue-related self-efficacy (FSE). Through experience sampling methodology (ESM) via the Booster smartphone app, Booster helps users gain personalised insight into the relationship between their thoughts, feelings, activities, and fatigue. Based on this insight and shared-decision making, the participant and executive investigator set personal lifestyle goals, such as more exercise and fewer daytime naps. The previous version of Booster, PROfeel, has already been shown effective in treating persistent fatigue in youth. Booster's value as an early intervention has yet to be studied. To better suit this aim and align with user preferences, the new Booster app includes features like goal attainment assistance, daily outcome tracking, and motivating game mechanics (e.g., rewards and a minigame). This protocol describes a study to examine the effect of Booster on FSE and the other study outcomes fatigue, school participation, life satisfaction, and perceived health. The secondary aim is to explore individual differences regarding (moment of) changes in outcomes during the Booster intervention.

METHODS

It is a single-centre study with a multiple baseline single-case experimental design (SCED). We aim to include twenty adolescents ages 12 to 18 years with a chronic health condition and fatigue. Booster's effect on outcomes will be measured with a daily survey during Phase A (baseline) and B (intervention). The start of phase B will be randomised across cases. The effect will be assessed with the multiple baseline single-case randomisation test (SCRT) at the group level. Additionally, at the single-case level, we will explore change using permutation distancing tests (PDTs), single-case interrupted time series analysis (ITSA), and change point analyses. Also, we will assess participant characteristics associated with (long-term) improvements.

DISCUSSION

Booster uses innovative methods by combining tailored ESM-insight, mHealth and healthcare professional support. Group-level analysis, strengthened by single-case observational analyses, will evaluate the effectiveness of ESM-supported blended care as an early fatigue intervention and identify its potential working mechanisms. It lays the groundwork for implementing ESM tools in clinical practice.

TRIAL REGISTRATION

ClinicalTrials, NCT06562335. Registered on 24 July 2024, https://clinicaltrials.gov/study/NCT06562335 .

摘要

背景

疲劳是患有慢性健康问题的青少年的常见症状。通过使用“助力器”(Booster)进行早期干预,可以预防持续性疲劳及其带来的损害。“助力器”是一种跨诊断混合护理干预措施,旨在提高与疲劳相关的自我效能感(FSE)。通过“助力器”智能手机应用程序的经验抽样方法(ESM),“助力器”帮助用户深入了解自己的思想、感受、活动和疲劳之间的关系。基于这一认识并通过共同决策,参与者和执行研究者设定个人生活方式目标,如增加锻炼和减少白天小睡。“助力器”的前一个版本PROfeel已被证明在治疗青少年持续性疲劳方面有效。“助力器”作为早期干预措施的价值尚未得到研究。为了更好地适应这一目标并符合用户偏好,新的“助力器”应用程序包括目标达成协助、每日结果跟踪和激励游戏机制(如奖励和小游戏)等功能。本方案描述了一项研究,以检验“助力器”对FSE以及其他研究结果疲劳、学校参与度、生活满意度和感知健康的影响。次要目标是探索在“助力器”干预期间结果(变化时刻)的个体差异。

方法

这是一项采用多基线单病例实验设计(SCED)的单中心研究。我们的目标是纳入20名年龄在12至18岁之间、患有慢性健康问题且有疲劳症状 的青少年。在A阶段(基线)和B阶段(干预)期间,将通过每日调查来衡量“助力器”对各项结果的影响。B阶段的开始时间将在各病例间随机确定。将在组水平上使用多基线单病例随机化检验(SCRT)评估效果。此外,在单病例水平上,我们将使用置换距离检验(PDT)、单病例中断时间序列分析(ITSA)和变化点分析来探索变化情况。我们还将评估与(长期)改善相关的参与者特征。

讨论

“助力器”通过结合量身定制的ESM洞察、移动健康和医疗专业支持,采用了创新方法。通过单病例观察分析得到加强的组水平分析,将评估ESM支持的混合护理作为早期疲劳干预措施的有效性,并确定其潜在的作用机制。它为在临床实践中应用ESM工具奠定了基础。

试验注册

ClinicalTrials,NCT06562335。于2024年7月24日注册,https://clinicaltrials.gov/study/NCT06562335

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