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临床试验/NCT02517047
NCT02517047已完成不适用

Community Empowerment to Pilot a Novel Device for Monitoring Rescue Medication Use in Urban Children With Asthma

Boston Children's Hospital2 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2016年3月最近更新:
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
26
试验地点
2
主要终点
Number of Participants With Rescue Inhaler Use

研究概览

简要总结

Background: Pediatric asthma is the most common chronic illness among children and is associated with poor quality of life, activity restriction, school absences, and thousands of physician visits annually. The purpose of this study is to measure the effectiveness of using an innovative tracking system (CareTRx) for the self-management of asthma, including daily and rescue medication use, among children and adolescents with pediatric asthma.

详细描述

The primary study objective is to measure the effectiveness of using an innovative tracking system (CareTRx) for the self-management of asthma, including daily and rescue medication use, among children with asthma. The study objectives will be achieved using a pre-post design for the participants. The investigators aim to enroll at least 26 participants for a 3-month intervention period. With this pilot study, the investigators hope to examine the impact of self-management behaviors on health outcomes including asthma symptoms and quality of life measures.

研究设计

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

入排标准

年龄范围
6 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Youth with a primary diagnosis of persistent asthma according by NHLBI criteria
  • Females or males between the ages of 6-17 years of age
  • Youth or caregiver must have an Android smart phone with operating system 4.3 or above and data plan for the duration of the study period

排除标准

  • Youth with other cardiac, pulmonary, or neuromuscular disorders that impact breathing
  • Youth with documented developmental delays or impairments that would interfere with ability to use CareTRx system

研究组 & 干预措施

CareTRx Device

Experimental

Subject will receive CareTRx device for rescue inhaler as well as the application downloaded to their Android phone. The device will track when the rescue inhaler is administered. The information will then be loaded to phone app.

干预措施: CareTRx (Device)

结局指标

主要结局

Number of Participants With Rescue Inhaler Use

时间窗: 12 weeks

Total number participants with rescue inhaler use throughout the course of the study.

Number of Participants With Daily Medication Compliance

时间窗: 12 weeks

Total number participants who took their medication as planned will be measured. This will include measuring the number of participants with medication compliance who take their medications as planned based on the data from the monitoring device.

次要结局

  • Asthma Symptoms(12 weeks)
  • Forced Expiratory Volume(Baseline)

研究者

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

Wanda Phipatanakul

Principle Investigator

Boston Children's Hospital

研究点 (2)

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