跳至主要内容
临床试验/NCT06998888
NCT06998888招募中不适用

Determining the Effectiveness of Remote Monitoring of Cancer Patients Undergoing Outpatient Oral Cancer Treatment Using Caaring® Software

Persei Vivarium6 个研究点 分布在 1 个国家目标入组 194 人开始时间: 2025年4月11日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
194
试验地点
6
主要终点
Percentage of adherence to treatment prescribed for cancer

研究概览

简要总结

The goal of this clinical trial investigation with device is to determinate the efficacy of the remote monitoring in cancer patients with a software called Caaring® a través del cumplimento terapéutico y de dosis.

The main question it aims to answer is if the development of a self-management platform (Caaring®) empowers cancer patients throughout their illness, reducing the number of in-person and telephone visits assisted by specialized medical and nursing staff. For this, researchers will compare the assessments between the two groups.

This is a randomized study with two arms. Online telemonitoring group: The follow-up of these patients will be carried out prospectively remotely through the Caaring® platform. And Prospective Control group: The data of these patients are collected prospectively for their routine medical visits for 12 weeks after their inclusion.

Caaring group patients must have sufficient technological skills to use a smartphone.

详细描述

This is a longitudinal, comparative non-inferiority, multicenter, with 2 arms Medical Device Clinical Trial.

The protocol and informed consent documents have been reviewed and approved by the hospital human subjects reviewboard and the study will be performed in accordance with the Declaration of Helsinki

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

  • Patients who provide informed consent.
  • Age ≥18 years.
  • Oncology patients undergoing active outpatient oral therapy with: capecitabine, cyclin inhibitors, hormonal therapies, TKI inhibitors, monotherapy with or without intravenous therapy.
  • Oncology patients undergoing active outpatient oral oncology treatment expected within 12 weeks of inclusion.
  • Patients who must demonstrate sufficient technological skills to operate a smartphone through the "technological skills questionnaire."
  • Patients who do not meet the

排除标准

  • Exclusion Criteria:
  • Patients with cognitive or sensory difficulties or insufficient command of Spanish language that, in the opinion of the healthcare professional conducting the recruitment, makes it difficult to understand the questions posed in the surveys, scales, or instruments used in the study, provided they do not have a legal representative capable of participating in the study.
  • Patients for whom it is anticipated that follow-up will not be possible due to a change of residence.
  • Patients who are participating in any other clinical trial or experimental study at the time of recruitment. Participation in observational studies will not be an exclusion criteria.
  • Patients whose primary diagnosis is a mental illness or another poorly controlled medical condition.
  • Terminally ill patients and/or those receiving palliative care according to the criteria of SECPAL (Spanish Society of Palliative Care).
  • Institutionalized patients.
  • Patients who, according to the recruiting professional's assessment, are not considered eligible for inclusion because they are undergoing specific follow-up care in other units (hemodialysis, transplants, etc.) requiring mandatory hospital visits less frequently than once every two months.
  • Patients who do not demonstrate sufficient technological skills to use a smartphone through the "technological skills questionnaire."

结局指标

主要结局

Percentage of adherence to treatment prescribed for cancer

时间窗: 12 weeks

The Percentage of adherence to treatment prescribed for cancer will be calculed: Units minus unused units, multiplied by 100

次要结局

  • Percentage of patients with al least 80% of data completed(Week 12)
  • Percentage of patients with 100% of data completed(Week 12)
  • Changes in the use of health resources(Day 0 and Monthly up to 12 weeks)
  • Patient satisfaction with the software Caaring(Week 12)

研究者

发起方
Persei Vivarium
申办方类型
Other
责任方
Sponsor

研究点 (6)

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