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Evaluating a digital tool for supporting breast cancer patients: a randomized controlled trial protocol (ADAPT)

机译:评估支持乳腺癌患者的数字工具:随机对照试验方案(适应)

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BACKGROUND:There are a growing number of mHealth tools for breast cancer patients but a lack of scientific evidence for their effects. Recent studies have shown a mix of positive and negative impacts on users. Here we will assess the impact of OWise Breast Cancer, a mobile application for self-monitoring symptoms and managing care, on the process of self-management.METHODS:This randomized controlled trial with early stage breast cancer patients will assess the effect of OWise use on patient activation at 3?months from diagnosis measured by the PAM-13 questionnaire. We will also assess differences in changes in health-related quality of life, psychological distress, health status, and National Health Service (NHS) health resource utilization over the first year from diagnosis. Participants will be randomly allocated (1:1) to standard care or standard care plus OWise. Participants will complete questionnaires before starting anti-cancer treatment and at 3, 6, and 12?months from diagnosis. Clinical and patient-reported outcome data will be linked to health resource utilization data from Discover, an integrated care record of primary, secondary, and social care in North West London. We will measure contamination in the control group and adjust the sample size to mitigate the dilution of effect estimates. A per-protocol analysis will be conducted as a sensitivity analysis to assess robustness of the primary results.DISCUSSION:This study aims to generate evidence for the effectiveness of OWise at improving patient activation for women with early-stage breast cancer. The results will show the impact of using the tool at the patient level and the NHS health system level. The outcomes of the study will have implications for the application of OWise across the NHS for breast cancer patients and expansion into other tumor types. Assessing publicly available mHealth tools poses a challenge to trialists due to the risk of contamination. Here we apply various methods to measure, mitigate, and assess the effects of contamination.TRIAL REGISTRATION:The study was registered at clincaltrials.gov (NCT03866655) on 7 March 2019.
机译:背景:乳腺癌患者的MHEATH工具​​越来越多,但缺乏科学的效果。最近的研究显示了对用户的积极和负面影响的混合。在这里,我们将评估IONASE乳腺癌的影响,是自我管理过程中的自我监测症状和管理护理的移动应用。方法:这种随机对照试验与早期乳腺癌患者将评估局限性的效果在患者激活3月份,由PAM-13问卷测量的诊断。我们还将评估第一年诊断中的健康有关的生活质量,心理困扰,健康状况和国家卫生资源(NHS)健康资源利用的差异。参与者将被随机分配(1:1)标准护理或标准护理加上欠款。参与者将在开始抗癌治疗之前完成调查问卷,并在3,6和12个月内完成诊断。临床和患者报告的结果数据将与来自Discover的卫生资源利用数据相关联,伦敦西北部的主要,中学和社会护理综合护理记录。我们将测量对照组的污染,并调整样品大小以减轻效果估计的稀释。每协议分析将作为敏感性分析进行,以评估初级结果的鲁棒性。分发:本研究旨在为欠早期乳腺癌改善患者激活的患者激活而产生证据。结果将显示使用该工具在患者水平和NHS卫生系统水平上的影响。该研究的结果将对乳腺癌患者的NHS跨越NHS的局限性的影响以及扩张成其他肿瘤类型。评估公开的MHEHEATH工具​​由于污染风险而对试验主义者提出挑战。在这里,我们应用了各种方法来衡量,减轻和评估污染的影响.TRIAL注册:该研究于2019年3月7日在Clincaltrials.gov(NCT03866655)中注册。

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