跳至主要内容
临床试验/NL-OMON50372
NL-OMON50372已完成不适用

Acceptance and potential clinical added value of Sense-IT in psychiatric patients with autism spectrum disorder and/or intellectual disability and/or borderline personality disorder: a proof-of-concept study. - Sense-IT in forensic psychiatric patients with ASD and/or ID and/or BPD

niversiteit Twente0 个研究点目标入组 25 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
25

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • Patients with ASD and/or ID
  • In order to be eligible to participate in this study, a subject must meet all
  • of the following criteria:
  • 1) is admitted to inpatient care at FPA De Boog, GGNet, Warnsveld
  • 2) is diagnosed with ASD and/or ID according to DSM-5 criteria (APA,
  • 3) is mentally competent and willing to participate in the study
  • Patients with BPD
  • In order to be eligible to participate in this study, a subject must meet all
  • of the following criteria:
  • 1) is admitted to inpatient care at Scelta, GGNet, Apeldoorn
  • 2) is diagnosed with BPD according to DSM-5 criteria (APA, 2013)
  • 3) is mentally competent and willing to participate in the study
  • In order to be eligible to participate in this study, a subject must meet all
  • of the following criteria:
  • 1) is working at FPA De Boog, GGNet or at Scelta, GGNet

排除标准

  • A potential subject who meets any of the following criteria will be excluded
  • from participation in this study:
  • 1) is unable to read, speak or write the Dutch language
  • 2) is using beta-blockers, Nurses
  • A potential subject who meets any of the following criteria will be excluded
  • from participation in this study:
  • 1) is unable to read, speak or write the Dutch language.

研究者

发起方
niversiteit Twente

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