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临床试验/NCT01663610
NCT01663610已完成不适用

Online Course for Adults With ADHD or Subclinical ADHD Teaching How to Use a Smartphone as a Support in Their Everyday Life

Karolinska Institutet2 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2012年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
58
试验地点
2
主要终点
Change (from baseline) in symptoms of inattention and concentration

研究概览

简要总结

This study is a randomized controlled trial (RCT) to evaluate the effect of an internet-based, guided self-help course for individuals who have recivied an ADHD diagnsis or struggle with organizing daily life and/or easily get distracted. The course (vardagsSMART) teach the participants how to use a Smartphone to better organize their everday life and will be compared to a wait list control group (CONT) that later will recieve the same course without guidance from a supervisor(selfSMART). It is hypothesized that VardagsSMART will be superior to CONT on ability to organize everyday life and ADHD-symptoms, and that vardagsSMART will be superior to selfSMART on adherence, understanding and perecived usefullness.

详细描述

Smartphones have a potential to improve the life of individuals who have major problems with structure and remembrance of everyday tasks. The automation by smartphones of these tasks away from caregivers to the individual is a process that is both time saving and positive for the individuals sense of autonomy.

There is too little research to date to say with clarity that smartphones is this tool for most of the patient group but many patients with ADHD report that a smartphone system for organisation and remembrance is a key that helps many live a more meaningful life.

The best way to teach these skills has not yet been proven. There is a clear advantage with teaching courses concerning IT in an online setting since hyperlinks and other texts can be easily forwarded and the course participants can easily use premade calendars and other tools. This research will try to determine if this type of online course is helpful for these patients.

VardagsSMART is an online course which will be compared to a waiting list controll group (CONT) which weekly records how they manage their ADHD symptoms.

The main purpose of this study is to examine whether the VardagsSMART course have a positive effect for the patient group. An untreated control group is used to ensure that the effects are not only due to spontaneous improvement. The control group will afterwards be offered the course without therapist support (SelfSMART), in order to make a preliminary evaluation of the importance of therapist support.

研究设计

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

  • have problems organizing daily activity measured by more then 17 points on the ASRS questionaire item 1-4 and 7-11-
  • has acces to a smartphone (android or iphone) with internet acces.
  • at least 18 years
  • speaks, writes and read Swedish
  • can not foresee any practical barriers to participation.

排除标准

  • has a high alcohol or drug use assessed by the AUDIT / DUDIT and assessment interview.
  • somatic or psychiatric problems that are directly contraindicated or seriously hamper the implementation of the treatment (eg, psychotic disorders).
  • have severe depression, defined as MADRS-S over 30 or suicidal risk judged by more than 4 points on the MADRS-S question 9 or according to the structured telephone assessment.
  • currently undergoing some form of treatment that focuses on reducing symptoms of ADHD.

结局指标

主要结局

Change (from baseline) in symptoms of inattention and concentration

时间窗: 6 weeks (Post) and 9 months (FU)

Adult Self Report Scale (ASRS), the subscale measuring inattention and concentration (item 1-4 and 7-11)

次要结局

  • Change (from baseline) in dialy life function(6 weeks (Post) and 9 months (FU))
  • Change (from baseline) in Depression and Anxiety(6 weeks (Post) and 9 months (FU))
  • Change (from baseline) in ADHD symptoms(6 weeks (Post) and 9 months (FU))
  • Change (from baseline) in perecived stress(6 weeks (Post) and 9 months (FU))

研究者

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

Viktor Kaldo

Principal Investigator

Karolinska Institutet

研究点 (2)

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