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临床试验/NCT02519946
NCT02519946已完成不适用

On-Line Intervention to Lower Cardiovascular Risk in Pediatric Heart Transplant Patients

Stanford University2 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2015年8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
14
试验地点
2
主要终点
Change in Endothelial Pulse Amplitude Testing Index

研究概览

简要总结

Pediatric heart transplant patients have a high-risk cardiovascular profile affecting their long-term outcomes and survival. Currently, no effective cardiovascular preventative care is provided for this pediatric population, in part, due to the fact that clinic-based programs are not easily accessible to children and their families. However, tele-health has been show to improve medical outcomes by making care more accessible to these patients. This study aims to meet the urgent need for an effective and sustainable delivery of preventative care to pediatric heart transplant patients using a diet and exercise intervention program delivered live over the internet direct to these patients' homes.

研究设计

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

入排标准

年龄范围
9 Years 至 19 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Heart transplant >11 months before baseline visit
  • Able to fast overnight
  • Cardiac clearance to exercise by the primary cardiologist
  • Presence of an adult at home during the exercise training sessions for patients < 14 years of age

排除标准

  • Acute illness
  • Latex allergy
  • Document transplant rejection < 3 months
  • Re-transplantation or multi-organ transplantation
  • Malignancy

研究组 & 干预措施

On-Line Diet and Exercise Intervention

Experimental

干预措施: On-Line Diet and Exercise Intervention (Other)

结局指标

主要结局

Change in Endothelial Pulse Amplitude Testing Index

时间窗: Baseline, 16 weeks, and 32 weeks

Test of endothelial function

次要结局

  • Arterial Tonometry(Baseline, 16 weeks, and 32 weeks)
  • Carotid Artery Imaging(Baseline, 16 weeks, and 32 weeks)
  • Fasting Low-Density Lipoprotein Level(Baseline, 16 weeks, and 32 weeks)
  • Volume of Oxygen Consumed at Maximal Exertion(Baseline, 16 weeks, and 32 weeks)
  • Physical and Psychosocial Health Questionnaire Scores(Baseline, 16 weeks, and 32 weeks)
  • Functional Movement Screening Score(Baseline, 16 weeks, and 32 weeks)

研究者

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

Seda Tierney

Principal Investigator

Stanford University

研究点 (2)

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