跳至主要内容
临床试验/NL-OMON49609
NL-OMON49609已完成不适用

Touch; reducing pain in Parkinson patients study 1 - Touch; reducing pain in Parkinson patients study 1

niversiteit Utrecht0 个研究点目标入组 35 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
入组人数
35

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • -Age >=18
  • -Diagnosed with PD, confirmed by ParkinsonNEXT and if necessary; i.e. inclusion
  • criteria are unclear or the experimenter still has some questions, the
  • experiment will check with the patient*s general practitioner.
  • -Pain associated with PD (musculoskeletal, dystonic, akathisia) and pain
  • worsened by PD (i.e. (osteo)arthritis or other age related pain conditions)
  • -Pain must be present for at least 3 months, with clear impact on
  • physical/psychological functioning, which must be assessed as at least moderate
  • in intensity (>=4 points on an 11-point Likert pain scale).
  • -Written informed consent (to assess whether participants are able to give
  • informed consent the MoCa will be used prior to intervention).

排除标准

  • -Incapability of giving informed consent
  • -Incapability of interpreting questionnaires
  • The following criteria will be checked for and confirmed by ParkinsonNEXT and
  • if necessary; i.e. inclusion criteria are unclear or the experimenter still has
  • some questions, the experiment will check with the patient*s general
  • practitioner:
  • -Suffering from conditions that affect the ability to feel or process touch
  • -Pain conditions that can also influence the perception and processing of
  • touch; i.e. Neuropathic pain;
  • -A history of cerebral traumata or psychiatric disorders unrelated to PD (e.g.,
  • schizophrenic episodes)
  • -Currently suffering from a mood disorder (e.g. depression or anxiety disorder)

研究者

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