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临床试验/NL-OMON55629
NL-OMON55629已完成不适用

The role of nocebo effects in identifying patients at risk for pain progression in fibromyalgia - Nocebo effects in fibromyalgia pain progression

niversiteit Leiden0 个研究点目标入组 75 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
75

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 64(—)

入选标准

  • 18-65 years old female
  • Good understanding of written and spoken Dutch
  • Additionally for Patients:
  • Diagnosis of fibromyalgia (provided by a rheumatologist)

排除标准

  • For patients:
  • Physical conditions other than fibromyalgia explaining pain symptoms
  • Psychiatric conditions not related to fibromyalgia symptoms (e.g.,
  • schizophrenia)
  • Use of painkillers different than usual dose of treatment on the day of
  • experimentation*
  • For healthy controls:
  • Chronic pain complaints (>=3 months) in the past or present or a diagnosis of
  • fibromyalgia
  • Severe physical or psychiatric co-morbidities that may interfere with the study
  • protocol (e.g., DSM-V diagnosis)
  • Current pain (>=3/10 on the Numeric Rating Scale) on the day of experimentation*
  • Use of painkillers within 24 hours before the day of experimentation*
  • Common criteria for both groups:
  • Pregnancy or lactation
  • Color blindness
  • Injuries/open wounds on the non-dominant hand or arm*
  • Carrying a pacemaker/implanted pumps
  • Having implanted metals on the non-dominant hand or arm
  • Refusal to remove artificial nails, nail polish, or any other substance
  • covering the thumbnail*
  • Unsuccessful pressure calibration, i.e., not being able to stably distinguish
  • relevant pressure intensities
  • *Exclusion criteria marked with a * pertain to the day of testing. In case one
  • or more of these criteria are met at the day of testing, the appointment will
  • be rescheduled if possible.

研究者

发起方
niversiteit Leiden

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