Spahrkäs Simon S, Looijmans Anne, Sanderman Robbert, Hagedoorn Mariët
Department of Health Psychology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
Department of Psychology, Health & Technology, University of Twente, Enschede, Netherlands.
JMIR Res Protoc. 2020 Feb 14;9(2):e15969. doi: 10.2196/15969.
Many cancer patients and survivors worldwide experience disabling fatigue as the main side effect of their illness and the treatments involved. Face-to-face therapy is effective in treating cancer-related fatigue (CRF), but it is also resource-intensive. Offering a self-management program via a mobile phone app (ie, the Untire app), based on elements of effective face-to-face treatments, might increase the number of patients receiving adequate support for fatigue and decrease care costs.
The aim of this protocol is to describe a randomized controlled trial (RCT) to assess the effectiveness of the Untire app in reducing fatigue in cancer patients and survivors after 12 weeks of app use as compared with a waiting list control group. Substudies nested within this trial include questions concerning the reach and costs of online recruitment and uptake and usage of the Untire app.
The Untire app study is a waiting list RCT targeting cancer patients and survivors who experience moderate to severe fatigue via social media (Facebook and Instagram) across 4 English-speaking countries (Australia, Canada, the United Kingdom, and the United States). The Untire app includes psychoeducation and exercises concerning energy conservation, activity management, optimizing restful sleep, mindfulness-based stress reduction, psychosocial support, cognitive behavioral therapy, and physical activity. After randomization, participants in the intervention group could access the Untire app immediately, whereas control participants had no access to the Untire app until the primary follow-up assessment at 12 weeks. Participants completed questionnaires at baseline before randomization and after 4, 8, 12, and 24 weeks. The study outcomes are fatigue (primary) and quality of life (QoL; secondary). Potential moderators and mediators of the hypothesized treatment effect on levels of fatigue and QoL were also assessed. Link clicks and app activation are used to assess reach and uptake, respectively. Log data are used to explore the characteristics of app use. Sample size calculations for the primary outcome showed that we needed to include 164 participants with complete 12-week measures both in the intervention and the control groups. The intention-to-treat approach is used in the primary analyses, which refers to analyzing all participants regardless of their app use.
Participants were recruited from March to October 2018. The last participant completed the 24-week assessment in March 2019.
This mobile health (mHealth) RCT recruited participants online in multiple countries to examine the uptake and effectiveness of the Untire self-management app to reduce CRF. Many advantages of mHealth apps are assumed, such as the immediate access to the app, the low thresholds to seek support, and the absence of contact with care professionals that will reduce costs. If found effective, this app can easily be offered worldwide to patients experiencing CRF.
Netherlands Trial Register NL6642; https://www.trialregister.nl/trial/6642.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/15969.
全球许多癌症患者及幸存者都经历着致残性疲劳,这是他们疾病及相关治疗的主要副作用。面对面治疗在治疗癌症相关疲劳(CRF)方面有效,但资源消耗大。基于有效面对面治疗的要素,通过手机应用程序(即Untire应用程序)提供自我管理项目,可能会增加获得疲劳充分支持的患者数量,并降低护理成本。
本方案的目的是描述一项随机对照试验(RCT),以评估与等待名单对照组相比,使用Untire应用程序12周后,该应用程序在减轻癌症患者及幸存者疲劳方面的有效性。嵌套在该试验中的子研究包括有关在线招募的覆盖范围和成本以及Untire应用程序的使用和采用情况的问题。
Untire应用程序研究是一项等待名单RCT,目标是通过社交媒体(Facebook和Instagram)在4个英语国家(澳大利亚、加拿大、英国和美国)招募经历中度至重度疲劳的癌症患者及幸存者。Untire应用程序包括有关能量节约、活动管理、优化安稳睡眠、基于正念的减压、心理社会支持、认知行为疗法和体育活动的心理教育及练习。随机分组后,干预组参与者可立即使用Untire应用程序,而对照组参与者在12周的主要随访评估前无法使用Untire应用程序。参与者在随机分组前的基线以及4周、8周、12周和24周后完成问卷。研究结果为疲劳(主要)和生活质量(QoL;次要)。还评估了假设的治疗效果对疲劳水平和QoL的潜在调节因素和中介因素。链接点击量和应用程序激活量分别用于评估覆盖范围和采用情况。日志数据用于探索应用程序使用的特征。主要结局的样本量计算表明,干预组和对照组均需要纳入164名有完整12周测量数据的参与者。主要分析采用意向性分析方法,即分析所有参与者,无论其是否使用应用程序。
参与者于2018年3月至10月招募。最后一名参与者于2019年3月完成了24周评估。
这项移动健康(mHealth)RCT在多个国家在线招募参与者,以检验Untire自我管理应用程序减轻CRF的采用情况和有效性。假定移动健康应用程序有许多优点,如可立即访问应用程序、寻求支持的门槛低以及无需与护理专业人员接触,这将降低成本。如果该应用程序被证明有效,可轻松地在全球范围内提供给经历CRF的患者。
荷兰试验注册库NL6642;https://www.trialregister.nl/trial/6642。
国际注册报告标识符(IRRID):DERR1-10.2196/15969。