跳至主要内容
临床试验/NCT03982017
NCT03982017终止不适用

Heart Failure Self-care Mobile Application to Reduce Readmissions Trial

University of Pittsburgh2 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2019年7月12日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
32
试验地点
2
主要终点
Time to readmission

研究概览

简要总结

This is a patient-centered comparative effectiveness feasibility pilot designed to examine an intervention to increase heart failure self-care and symptom recognition. The investigators will randomize 100 participants to receive either usual care at the time of discharge after heart failure admission or a smartphone application that enhances self-care.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
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

  • Inpatient admission for acute decompensated heart failure
  • Left ventricular systolic or diastolic heart failure
  • Owns a smartphone with a data plan

排除标准

  • Hospice or life expectancy less than 6 months
  • Palliative inotrope use
  • Heart transplant listed, or status post transplant
  • Ventricular assist devise present, or awaiting placement
  • Not being discharged to home
  • Unable to provide consent or comply with the intervention
  • Current enrollment in a remote monitoring/ telehealth program

结局指标

主要结局

Time to readmission

时间窗: from the date of enrollment until the date of first documented admission or date of death from any cause, whichever comes first, assessed up to 90 days

time to readmission

Kansas City Cardiomyopathy Questionnaire at 30 days post enrollment

时间窗: 30 days post index discharge

Quality of life, subjective level of function

Percent of participants readmitted within 30 days

时间窗: 30 days post index discharge

30-day readmission rate as determined by participant report or medical record query

Percent of participants readmitted within 90 days

时间窗: 90 days post index discharge

90-day readmission rate as determined by participant report or medical record query

Kansas City Cardiomyopathy Questionnaire at 90 days post enrollment

时间窗: 90 days post index discharge

Quality of life, subjective level of function

次要结局

未报告次要终点

研究者

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

Amber Johnson

Assistant Professor

University of Pittsburgh

研究点 (2)

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