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临床试验/NCT02165423
NCT02165423已完成不适用

Discharge to Home and Chronic Illness Care Pilot

Medical College of Wisconsin2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2014年6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
20
试验地点
2
主要终点
Evaluate the effectiveness of myFAMI on 30-day post-discharge outcomes.

研究概览

简要总结

The purpose of this study is to address a gap in knowledge needed for care of children with solid organ transplantation (SOT) and their parents by combining mHealth technology with an individualized family centered self-management intervention (referred to as myFAMI). This study is critical to the increased understanding of hospital to home transition and family management at home with the potential to transform the way clinicians approach the care of complex chronic illness children and families.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Health Services Research
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • parent's child has undergone a heart, kidney, or liver transplant and is being discharged home from the hospital
  • the parent is English speaking (to date the tools being used have been validated for English participants only)
  • parent is 18 years of age or older
  • patient is 17 years of age and younger.

排除标准

  • presence of significant communication or cognitive impairment on the part of the parent that would preclude completion of questionnaires based on self-report
  • parent and child has experienced the discharge to home transition from a previous transplant.

研究组 & 干预措施

Control

Experimental

Ten parents will be randomized to the control group defined as 'usual care' and ten to the intervention group, stratified by type of transplant.

干预措施: myFAMI iPad application (Behavioral)

Intervention

Experimental

Ten parents will be randomized to the control group defined as 'usual care' and ten to the intervention group, stratified by type of transplant.

干预措施: myFAMI iPad application (Behavioral)

结局指标

主要结局

Evaluate the effectiveness of myFAMI on 30-day post-discharge outcomes.

时间窗: 30 days following enrollment

Hypothesis: Compared to parents who received standard discharge preparation (usual care), parents receiving myFAMI will report: i) Better care coordination, ii) Higher quality of discharge teaching, iii) Greater readiness for hospital discharge, iv) Improved post-discharge coping, v) Improved family functioning, vi) Better self-management of medication and treatment regimens vii) Fewer emergency department visits and hospital readmissions

次要结局

  • Examine the acceptability of myFAMI:(Enrollment plus 30 days)

研究者

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

Stacee Lerret

Assistant Professor

Medical College of Wisconsin

研究点 (2)

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