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临床试验/NCT03616522
NCT03616522已完成不适用

A Prospective Study of Electronic Symptom Reporting Via Mobile Phone Among Patients With Advanced Non-Small Cell Lung Cancer

Abramson Cancer Center at Penn Medicine1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2018年5月21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
25
试验地点
1
主要终点
Number of subjects who will adhere to the mobile phone-based intervention

研究概览

简要总结

Symptoms are common among patients with advanced malignancy undergoing treatment, and yet often go unrecognized by treatment providers. In addition to contributing to morbidity, poorly controlled symptoms drive emergency room utilization and hospital admission in this population, representing significant cost to patients, families, and the health care system. Systematic collection of patient-reported outcomes (PROs) has been proposed as a way to arm providers with the information necessary to intervene early, intensify symptom management, and improve symptom control. Recent research suggests that a standardized, web-based program of weekly patient-reported symptom monitoring leads to improved health-related quality of life and reduced acute care utilization; it may also prolong overall survival. Despite mounting evidence supporting its use among oncology patients, systematic PRO collection is lacking at most cancer centers, and optimal models for collection of PROs are poorly understood. The objective of this study is to evaluate prospectively the feasibility of a novel mobile phone-based intervention of weekly symptom reporting, among patients undergoing treatment for advanced non-small cell lung cancer.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Adult patient (age ≥ 18 years) with advanced (metastatic) non-small cell lung cancer, initiating a new line of palliative-intent treatment at Abramson Cancer Center
  • Ability to read and respond to questions in English
  • Ability to provide informed consent to participate in the study
  • Access to a smart phone capable of SMS-text messaging and internet access

排除标准

  • Inability to read and respond to questions in English
  • Inability or unwillingness to provide informed consent to participate in the study
  • Inability to engage with SMS-text based platform
  • Current enrollment in a clinical trial

结局指标

主要结局

Number of subjects who will adhere to the mobile phone-based intervention

时间窗: 3 months

evaluate subjects to study-level adherence of a mobile phone-based intervention for automated PRO collection

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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