跳至主要内容
临床试验/NCT02833246
NCT02833246已完成不适用

Using a Patient-Centered mHealth Intervention to Improve Adherence to Oral Anticancer Medications

Memorial Sloan Kettering Cancer Center1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2016年6月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
28
试验地点
1
主要终点
objective pill count

研究概览

简要总结

This study is being done to determine if sending reminder text messages helps patients take their Oral Anticancer Medication (OAMs) when they are supposed to.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

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

  • Patient in the Sarcoma, Solid Tumor Gastrointestinal (ST GI), and Thoracic Medicine service at MSK.
  • Starting a new treatment regimen that includes a single oral anticancer medication
  • Patients must have a mobile phone that can send and receive SMS/MMS messages and is internet-enabled.
  • Age 18 or older.
  • Ability to speak and read English because we do not have the resources to translate the text messages into other languages.

排除标准

  • Patient expresses inability or unfamiliarity with using SMS/MMS messaging on their phone and is unwilling to be trained in the use of this technology.

研究组 & 干预措施

SMS/MMS text messaging

Experimental

Patients will be able to tailor their SMS/MMS reminders with respect to when (i.e., what time of day) they wish to receive the reminders, as well as how often the messages are sent (e.g., morning and evening).

干预措施: SMS/MMS text messaging (Other)

usual care

Active Comparator

This includes physician and nursing assessment and intervention for any identified AEs. Of note, there is not currently standard follow-up that patients receive from nursing or physician staff while on an OAM treatment. Patients are encouraged to call their physician's office with any questions or changes in their medical status but are not called routinely by MSK staff.

干预措施: usual care (Other)

结局指标

主要结局

objective pill count

时间窗: 1 year

is greater or less than the amount of OAM that the patient should have in their possession.

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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