Phillips Siobhan, Solk Payton, Welch Whitney, Auster-Gussman Lisa, Lu Marilyn, Cullather Erin, Torre Emily, Whitaker Madelyn, Izenman Emily, La Jennifer, Lee Jungwha, Spring Bonnie, Gradishar William
Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
JMIR Res Protoc. 2021 Apr 23;10(4):e24254. doi: 10.2196/24254.
Increased incidence and life expectancy have resulted in a growing population of patients with metastatic breast cancer, and these patients experience high rates of morbidity and premature mortality. Increased physical activity (PA) is consistently associated with improved health and disease outcomes among early-stage survivors. However, there is a paucity of research on PA in patients with metastatic breast cancer, and existing PA interventions have exhibited low feasibility because of their focus on intense PA and/or requirement of on-site visits. Mobile health (mHealth)-based PA interventions may be particularly useful for patients with metastatic breast cancer because they allow for remote monitoring, which facilitates individual tailoring of PA recommendations to patients' abilities and may minimize participant burden. However, no studies have examined mHealth PA interventions in patients with metastatic breast cancer.
We aim to address these critical research gaps by testing a highly tailored technology-based intervention to promote PA of any intensity (ie, light, moderate, or vigorous) by increasing daily steps in patients with metastatic breast cancer. The primary aim of this study is to test the feasibility and acceptability of the Fit2ThriveMB intervention. We will also examine outcome patterns suggesting the efficacy of Fit2ThriveMB on symptom burden, quality of life, and functional performance.
The Fit2ThriveMB trial is a two-arm pilot randomized controlled trial that will compare the effects of a smartphone-delivered, home-based PA intervention and an attention-control education condition on PA and quality of life in low-active female patients with metastatic breast cancer. A subsample (n=25) will also complete functional performance measures. This innovative trial will recruit 50 participants who will be randomized into the study's intervention or control arm. The intervention will last 12 weeks. The Fit2ThriveMB intervention consists of a Fitbit, coaching calls, and the Fit2ThriveMB smartphone app that provides self-monitoring, a tailored goal-setting tool, real-time tailored feedback, app notifications, and a group message board. Assessments will occur at baseline and post intervention.
The Fit2ThriveMB study is ongoing. Data collection ended in February 2021.
Data from this study will provide the preliminary effect sizes needed to assemble an intervention that is to be evaluated in a fully powered trial. In addition, these data will provide essential evidence to support the feasibility and acceptability of using a technology-based PA promotion intervention, a scalable strategy that could be easily integrated into care, among patients with metastatic breast cancer.
ClinicalTrials.gov NCT04129346; https://clinicaltrials.gov/ct2/show/NCT04129346.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/24254.
转移性乳腺癌患者的发病率上升和预期寿命延长,导致该患者群体不断增加,这些患者的发病率和过早死亡率很高。身体活动增加(PA)一直与早期幸存者的健康改善和疾病预后相关。然而,关于转移性乳腺癌患者PA的研究较少,现有的PA干预措施由于侧重于高强度PA和/或需要现场就诊,可行性较低。基于移动健康(mHealth)的PA干预措施可能对转移性乳腺癌患者特别有用,因为它们允许远程监测,这有助于根据患者的能力对PA建议进行个性化调整,并可能将参与者的负担降至最低。然而,尚无研究考察转移性乳腺癌患者的mHealth PA干预措施。
我们旨在通过测试一种高度个性化的基于技术的干预措施,以增加转移性乳腺癌患者的每日步数,促进任何强度(即轻度、中度或剧烈)的PA,来填补这些关键的研究空白。本研究的主要目的是测试Fit2ThriveMB干预措施的可行性和可接受性。我们还将检查结果模式,以表明Fit2ThriveMB对症状负担、生活质量和功能表现的疗效。
Fit2ThriveMB试验是一项双臂试点随机对照试验,将比较通过智能手机提供的家庭PA干预措施和注意力控制教育条件对低活动水平的转移性乳腺癌女性患者的PA和生活质量的影响。一个子样本(n = 25)还将完成功能表现测量。这项创新试验将招募50名参与者,他们将被随机分配到研究的干预组或对照组。干预将持续12周。Fit2ThriveMB干预措施包括一个Fitbit、指导电话以及Fit2ThriveMB智能手机应用程序,该应用程序提供自我监测、个性化目标设定工具、实时个性化反馈、应用程序通知和群组留言板。评估将在基线和干预后进行。
Fit2ThriveMB研究正在进行中。数据收集于2021年2月结束。
本研究的数据将提供在全面试验中评估干预措施所需的初步效应大小。此外,这些数据将提供重要证据,以支持基于技术的PA促进干预措施在转移性乳腺癌患者中的可行性和可接受性,这是一种可扩展的策略,可以轻松整合到护理中。
ClinicalTrials.gov NCT04129346;https://clinicaltrials.gov/ct2/show/NCT04129346。
国际注册报告识别码(IRRID):DERR1-10.2196/24254。