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临床试验/NCT03592771
NCT03592771已完成不适用

Communication App to Manage Symptoms and Improve Adjuvant Endocrine Therapy Adherence

Emory University4 个研究点 分布在 1 个国家目标入组 304 人开始时间: 2018年11月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
304
试验地点
4
主要终点
Adjuvant Endocrine Therapy (AET) Medication Adherence

研究概览

简要总结

This study will test the use of a web-enabled app that is integrated directly with patients' electronic health records, with and without tailored feedback. The app-based intervention is designed to improve patient-provider communication outside of clinic visits, resulting in improved symptom management and adjuvant endocrine therapy adherence among diverse patients with hormone receptor-positive breast cancer. The researchers will evaluate the impact of the intervention on a comprehensive set of outcomes, including rigorous measures of long-term adherence, quality of life, and costs.

详细描述

For women with hormone receptor-positive breast cancer, long-term use of adjuvant endocrine therapy (AET) significantly reduces the risk of hospitalizations, cancer recurrence and mortality, and increases quality of life. Despite the known benefits of AETs, many patients are nonadherent due to adverse side effects. Furthermore, lower AET adherence among black women may be contributing to the large and growing disparities in mortality outcomes. Real-time monitoring of treatment-related adverse symptoms and adherence could result in more effective management of symptoms, higher medication adherence, and ultimately lower recurrence and mortality. To date, however, only a few interventions have aimed to improve AET adherence, even fewer have targeted symptom management as a means to improve adherence, and none have found a statistically significant improvement on adherence. This study will fill this research gap by testing a web-enabled app designed with the explicit goal of improving long-term AET adherence. Patient-reported symptoms will be integrated directly with the patient's electronic health record, and concerning reports will trigger an alert to the patient's care team in order to improve timely patient-provider communication and care outside of clinic visits. In a small pilot trial of the study app, the researchers found that participants who had recently initiated a new AET and received weekly reminders to use the app reported significantly higher adherence to AETs at 8 weeks compared with a control group (91% vs. 68%, p=0.02). The proposed study builds on the success of the pilot by: 1) expanding the intervention period to six months in order to capture later-onset adverse symptoms that are slower to develop; 2) following participants for one to three years, depending on enrollment year, to test longer-term effects of the intervention on medication adherence and other outcomes; 3) including a larger sample powered to test multiple levels of the intervention; and 4) race-stratifying to test for a differential impact by race. This study will randomize 360 participants to one of three arms: 1) an "App" group (n=120) that will receive weekly reminders to use the study app; 2) an "App+Feedback" group (n=120) that will receive weekly reminders and personalized feedback based on their use of the app; or 3) a "Usual Care" group (n=120) that will receive usual care only. The app will include questions about AET adherence and adverse symptoms with built-in alerts sent to the patient's care team if any concerning symptoms or trends are reported. The researchers hypothesize that monitoring symptoms and adherence with actionable alerts and tailored feedback reports to patients will result in timelier symptom management and higher long-term adherence to AET. By evaluating the impact of the intervention on a comprehensive set of measures, including AET adherence, patient outcomes, racial disparities and resource use-related costs, this study will provide valuable and actionable results for providers, policy makers, and insurers who strive to achieve the "Triple Aim" - reduce costs while improving health outcomes and the patient experience.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 110 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Adult female patients (age≥18)
  • Diagnosis of ductal carcinoma in situ or Stage I-III hormone receptor-positive breast cancer
  • New prescription for an aromatase inhibitor or tamoxifen
  • Have a mobile device with a data plan or a home computer with Internet
  • Have a valid email address
  • Willing to complete brief surveys on a web-enabled device
  • AET is indicated as standard of care

排除标准

  • Unable to communicate in English
  • Prior use of adjuvant endocrine therapy (aromatase inhibitor or tamoxifen) for current diagnosis
  • Concurrently undergoing surgery, chemotherapy or radiation
  • Current diagnosis of rheumatoid arthritis
  • Chronic daily narcotic usage
  • Patient plans to move or transfer their care within the next year

结局指标

主要结局

Adjuvant Endocrine Therapy (AET) Medication Adherence

时间窗: Up to Month 12

Medication adherence with prescribed AET (aromatase inhibitor or tamoxifen) is captured using an electronic monitoring pillbox (Wisepill).

次要结局

  • Short Form Health Survey (SF-12) Mental Component Summary (MCS) Score(Baseline, Month 12)
  • 19 Item Endocrine Symptom Subscale (ESS-19) Score of the Functional Assessment of Cancer Therapy - Endocrine Symptoms (FACT-ES)(Baseline, Month 12)
  • Short Form Health Survey (SF-12) Physical Component Summary (PCS) Score(Baseline, Month 12)
  • Patient-Reported Outcomes Measurement Information System (PROMIS) Self-Efficacy for Managing Symptoms Score(Baseline, Month 12)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ilana Graetz

Associate Professor

Emory University

研究点 (4)

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