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临床试验/NCT03639233
NCT03639233已完成不适用

Youth Epilepsy and Successful Self-Management Intervention

University of Minnesota2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2018年10月1日最近更新:
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
120
试验地点
2
主要终点
Feasibility of recruiting and enrollment procedures and

研究概览

简要总结

This study is designed as a pilot test of the YESS! web-based intervention for adolescents with epilepsy. One hundred twenty participants will be given access to the intervention for a period of eight weeks. The investigators are testing the feasibility and acceptability of the the study procedures, measures and of the intervention itself. The study also evaluats the potential for impact on the users.

详细描述

YESS! is a web-based self management program developed to enhance the motivation and skills of youth with epilepsy.

This clinical trial uses a pre-test, post-test design where all consenting participants are given access to the intervention.

研究设计

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

入排标准

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

入选标准

  • Age as above
  • Epilepsy diagnosed by a physician
  • Currently taking anti-seizure medications or use device
  • Ability to understand and respond to questions about health and epilepsy
  • Ability to utilize an internet based intervention website

排除标准

  • 未提供

研究组 & 干预措施

Arm 1

Other

Intervention access

干预措施: YESS! (Behavioral)

结局指标

主要结局

Feasibility of recruiting and enrollment procedures and

时间窗: 8 weeks after getting access to the web intervention

Measure the extent to which the recruitment and enrollment procedures meet the study aims in terms of number of participants log in to the intervention

Acceptability of intervention website users

时间窗: 8 weeks after getting access to the web intervention

and the extent to which users (study subjects) find the intervention easy to use, enjoyable to use, useful, engaging. Acceptability is a multifaceted and complex concept. As such it it is best examined as a system of interacting attributes.

次要结局

  • Participant Well-being(8 weeks after getting access to the web intervention and 8 weeks after that.)
  • Participant Quality of Life(8 weeks after getting access to the web intervention and 8 weeks after that.)
  • self-management behavior profile(8 weeks after getting access to the web intervention and 8 weeks after that.)
  • self-management motivation profile(8 weeks after getting access to the web intervention and 8 weeks after that.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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