跳至主要内容
临床试验/DRKS00022534
DRKS00022534招募中不适用

Requirements analysis for a robotic assistive system to support and promote the autonomy of people with neuromuscular diseases - ArNe - Requirements Analysis

Forschungsgruppe Geriatrie - Charité Universitätsmedizin Berlin0 个研究点目标入组 15 人开始时间: 2020年11月4日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
15

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 Years 至 one(—)
性别
All

入选标准

  • •(a) patients with NME
  • •- Patients from the age of 18 years
  • •- Clinical diagnosis of a NME: possible, probable or confirmed ALS according to the revised elescorial criteria or clinically confirmed diagnosis of an infantile or juvenile form of spinal muscular atrophy (type I, II and III)
  • •- already supplied with a robotic system
  • •b) (nursing) relatives
  • •- at the age of 18 years
  • •- Persons who have a close personal relationship with the patient, come from the patient's family or extended environment and are significantly involved in the care process
  • •c) Nursing professionals
  • •- at the age of 18 years
  • •- registered carer or care assistant
  • •- Experience with the care of people with NME

排除标准

  • •(a) patients with MNE
  • •- lack of ability to consent (concomitant at least moderate dementia)
  • •- unwillingness to record pseudonymised personal and disease-related data
  • •- Severe auditory, visual, sensory and motor limitations
  • •- Psychiatric disorders (e.g. depression, anxiety and compulsions; substance-related disorders in the last 2 years, schizophrenia, other psychotic disorders)
  • •- Severe affective or cognitive disorders (Are you or have you been treated for a mental illness?)
  • •- No testing of or provision of robotic assistance system(s)
  • •b) (nursing) relatives
  • •- absence of consent
  • •- Existence of a significant psychological burden which makes the additional burden of interviewing appear unreasonable from a clinical point of view
  • •c) Nursing professionals
  • •- Lack of experience with the care of ALS patients

研究者

发起方
Forschungsgruppe Geriatrie - Charité Universitätsmedizin Berlin

相似试验