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.
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