Patient-Generated Health Data Collection During Chemoradiotherapy for Lung Cancer: A Pilot Study

The New York Proton Center2 个研究点分布在 1 个国家目标入组 40 人2024年3月22日

概览

简要总结

This is an observational study involving the collection of patient-generated health data using an Apple Watch, a home pulse oximeter, and a smartphone during a course of proton beam radiotherapy for lung cancer. The study period over which this information is collected will range from the day of study enrollment until two weeks after radiotherapy completion. Subjects will complete a short satisfaction survey at the end of the study period. Other information that is collected as part of routine care for this patient population will be extracted from subjects' medical records during the study period and afterwards.

详细描述

This is an observational study involving the collection of patient-generated health data using an Apple Watch, a home pulse oximeter, and a smartphone during a course of proton beam radiotherapy for lung cancer. The study period over which this information is collected will range from the day of study enrollment until two weeks after radiotherapy completion. Subjects will complete a short satisfaction survey at the end of the study period. Other information that is collected as part of routine care for this patient population will be extracted from subjects' medical records during the study period and afterwards. Primary Objective • To demonstrate the feasibility of patient-generated health data collection during thoracic proton beam radiotherapy for lung cancer. Secondary Objective • To demonstrate the face validity of physical activity and vital sign data collected during proton beam radiotherapy for lung cancer. Exploratory Objective • To explore associations between radiotherapy treatment parameters, wearable device data, patient-reported outcomes, adverse events, and long-term clinical outcomes.

注册库

clinicaltrials.gov

开始日期

2024年3月22日

结束日期

2031年3月21日

最后更新

19天前

研究类型

Observational

性别

All

研究者

发起方

The New York Proton Center

责任方

Sponsor

入排标准

入选标准

•Plan for fractionated (≥15 treatments) proton beam thoracic radiotherapy with curative intent for lung cancer
•Non-small cell lung cancer (NSCLC) or small cell lung cancer (SCLC) histology is permitted.
•Concurrent chemotherapy is permitted but not required..
•Previous thoracic radiotherapy is allowed.
•Ability to complete study surveys in English or Spanish
•Age \>/= 18
•Concurrent enrollment on other trials is permitted
•Patients who already use wearable devices and/or smartphones that monitor physical activity are eligible for this trial, provided they agree to utilize the devices provided by the study team during the study period
•All patients must sign study-specific informed consent prior to study entry

排除标准

•Ongoing treatment for another cancer that is expected to affect the toxicity profile of thoracic radiotherapy
•Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception; this exclusion is necessary because the treatment involved in this study may be significantly teratogenic

结局指标

主要结局

Demonstrate the feasibility of patient-generated health data collection during thoracic proton beam radiotherapy for lung cancer, based on the quantity of data collected from the day of radiotherapy initiation to the day of radiotherapy completion.

时间窗: 4-5 Weeks

Feasibility assessed based on the quantity of data collected from day of radiotherapy initiation to day of radiotherapy completion. The feasibility of physical activity data collection will be assessed based on usage information provided by the Apple Watch. Descriptive statistics to be used to report the distribution of average use times in the study cohort and the proportion of days subjects wear the Apple Watch for at least 8 hours. The feasibility of daily home pulse oximeter data collection reported using frequencies and percentages. The feasibility of weekly electronic PRO collection reported using frequencies and percentages.

次要结局

Demonstrate the face validity of physical activity and vital sign data collected in this trial by reviewing the distribution of values obtained for each measure quantitatively using descriptive statistics.(4-5 Weeks)