癌症患者适应性支持护理系统的可用性和初步疗效:试点随机对照试验。

IF 3.3 Q2 ONCOLOGY JMIR Cancer Pub Date : 2024-07-10 DOI:10.2196/49703
Sharon H Baik, Karen Clark, Marisol Sanchez, Matthew Loscalzo, Ashley Celis, Marianne Razavi, Dershung Yang, William Dale, Niina Haas
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引用次数: 0

摘要

背景:我们的团队采用以用户为中心的迭代设计流程,开发出了以患者为中心的自适应支持性护理系统 PatientCareAnywhere,该系统可为患者提供全面的生物心理社会筛查和自适应的癌症支持性护理。PatientCareAnywhere 的总体目标是提高癌症患者的健康相关生活质量(HRQOL)和自我效能,具体做法是让他们掌握自我管理技能,并直接在家中为他们提供癌症护理支持。这种支持可根据患者的需求和健康状况进行调整,并以转诊、教育、社区资源参与和安全的社会交流等形式从多个来源进行协调:本研究旨在评估新的基于网络的 PatientCareAnywhere 系统的可用性,并检验 PatientCareAnywhere 与常规护理相比在改善患者报告结果方面的初步效果:第一阶段的可用性测试参与者包括癌症患者(4 人)和护理人员(7 人),他们对软件原型进行了评估,并提供了定性(如访谈)和定量(如系统可用性量表)反馈。在第二阶段,为期 3 个月的试点随机对照试验的参与者被随机分配到接受 PatientCareAnywhere 干预(36 人)或常规护理对照条件(36 人)。在基线(干预前评估)和自基线起 12 周(干预后评估)对患者的 HRQOL 和癌症相关自我效能进行评估;比较两组患者干预前和干预后得分的平均差异:结果:参与者对原型非常满意,并表示可用性高于平均水平,系统可用性量表平均得分为 84.09(标准差 10.02)。定性数据支持干预措施的整体可用性和感知有用性,并根据参与者的反馈增加了一些设计功能(如 "帮助请求 "功能)。在随机对照试验方面,与对照组相比,干预组患者的 HRQOL 从干预前到干预后的评分有显著改善(平均差 6.08,标准差 15.26)(平均差 -2.95,标准差 10.63;P=0.01)。相比之下,自我效能感在组间无明显差异(P=.09):总体而言,PatientCareAnywhere 是一种用户友好型、功能性和可接受的支持性护理干预措施,对改善癌症患者的 HRQOL 具有初步疗效。未来的研究需要进一步确定 PatientCareAnywhere 的疗效,探索提高用户参与度的策略,研究干预的最佳强度、频率和使用方法,以改善患者的治疗效果:ClinicalTrials.gov NCT02408406; https://clinicaltrials.gov/study/NCT02408406。
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Usability and Preliminary Efficacy of an Adaptive Supportive Care System for Patients With Cancer: Pilot Randomized Controlled Trial.

Background: Using an iterative user-centered design process, our team developed a patient-centered adaptive supportive care system, PatientCareAnywhere, that provides comprehensive biopsychosocial screening and supportive cancer care to patients across the continuum of care adaptively. The overarching goal of PatientCareAnywhere is to improve health-related quality of life (HRQOL) and self-efficacy of patients with cancer by empowering them with self-management skills and bringing cancer care support directly to them at home. Such support is adaptive to the patient's needs and health status and coordinated across multiple sources in the forms of referrals, education, engagement of community resources, and secure social communication.

Objective: This study aims to assess the usability of the new web-based PatientCareAnywhere system and examine the preliminary efficacy of PatientCareAnywhere to improve patient-reported outcomes compared with usual care.

Methods: For phase 1, usability testing participants included patients with cancer (n=4) and caregivers (n=7) who evaluated the software prototype and provided qualitative (eg, interviews) and quantitative (eg, System Usability Scale) feedback. For phase 2, participants in the 3-month pilot randomized controlled trial were randomized to receive the PatientCareAnywhere intervention (n=36) or usual care control condition (n=36). HRQOL and cancer-relevant self-efficacy were assessed at baseline (preintervention assessment) and 12 weeks from baseline (postintervention assessment); mean differences between pre- and postintervention scores were compared between the 2 groups.

Results: Participants were highly satisfied with the prototype and reported above-average acceptable usability, with a mean System Usability Scale score of 84.09 (SD 10.02). Qualitative data supported the overall usability and perceived usefulness of the intervention, with a few design features (eg, "help request" function) added based on participant feedback. With regard to the randomized controlled trial, patients in the intervention group reported significant improvements in HRQOL from pre- to postintervention scores (mean difference 6.08, SD 15.26) compared with the control group (mean difference -2.95, SD 10.63; P=.01). In contrast, there was no significant between-group difference in self-efficacy (P=.09).

Conclusions: Overall, PatientCareAnywhere represents a user-friendly, functional, and acceptable supportive care intervention with preliminary efficacy to improve HRQOL among patients diagnosed with cancer. Future studies are needed to further establish the efficacy of PatientCareAnywhere as well as explore strategies to enhance user engagement and investigate the optimal intensity, frequency, and use of the intervention to improve patient outcomes.

Trial registration: ClinicalTrials.gov NCT02408406; https://clinicaltrials.gov/study/NCT02408406.

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来源期刊
JMIR Cancer
JMIR Cancer ONCOLOGY-
CiteScore
4.10
自引率
0.00%
发文量
64
审稿时长
12 weeks
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