跳至主要内容
临床试验/NCT05249283
NCT05249283已完成不适用

Self and Body Perception in Otoneurological Disorders: Translation and Validation of Measurement Scales

Hôpital Européen Marseille1 个研究点 分布在 1 个国家目标入组 612 人开始时间: 2022年3月31日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
612
试验地点
1
主要终点
Scores from the CDS questionnaire translated according to standardized methods (forward translation, back translation, consensus) in patients with other vestibular disorders and control subjects.

研究概览

简要总结

Depersonalization-derealization (DD) disorders are a clinical phenomenon characterized by feeling disconnected or detached from one's self. Individuals may report feeling as if they are an outside observer of their own thoughts or body, and often report feeling a loss of control over their thoughts or actions.

Several scales have been developed to measure DD, and the Cambridge Depersonalization Scale (CDS) appears to be the most relevant and consistent to characterize the clinical symptoms of these disorders as well as their duration and frequency. This scale, originally written in English, must be translated and validated according to standardized methods that include testing steps patients with dizziness and in individuals with no vestibular disorder.

Persistent postural-perceptual dizziness (PPPD) is a chronic, persistent vestibular syndrome generally preceded by acute vestibular disorders. The main symptoms are rotational dizziness, unsteadiness and / or non-rotating dizziness that are exacerbated by upright posture, walking, active or passive movement, and exposure to moving visual stimuli or complex visual patterns. To help diagnose this syndrome, a questionnaire was developed in Japan in 2019, the Niigata questionnaire, however no French version has yet been validated. Similarly, this scale needs to be validated in patient with PPPD and in control populations.

The main objective of this study is to validate the French translation of these two scales, the CDS questionnaire and the Niigata PPPD questionnaire, according to standard methods (forward translation, back translation, consensus).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • For patient:
  • Age ≥ 18 years
  • Patient with acute or chronic otoneurological disorders
  • Patient having or having experienced dizziness and / or balance disorders
  • Patient with PPPD
  • Fluency in French
  • Having given free and informed written consent
  • Being affiliated with or benefiting from social security
  • For control subjects:
  • Age ≥ 18 years
  • Fluency in French
  • Having given free and informed written consent
  • Being affiliated with or benefiting from social security.

排除标准

  • For patient:
  • Past or present psychiatric and neurological disease (other than otoneurological or PPPD, as declared by the participant)
  • For control subjects:
  • Past or present psychiatric and neurological disease (as declared by the participant) and vestibular and/or auditory system disorders (as declared by the participant)
  • For all participants:
  • Persons still in a period of exclusion from another study and persons simultaneously participating in another study
  • Subject to a measure for the protection of justice

结局指标

主要结局

Scores from the CDS questionnaire translated according to standardized methods (forward translation, back translation, consensus) in patients with other vestibular disorders and control subjects.

时间窗: 24 months

Scores from the Niigata PPPD questionnaire translated according to standardized methods (forward translation, back translation, consensus) in patients with PPPD, patients with other vestibular disorders and control subjects.

时间窗: 24 months

次要结局

  • Measurement of the HADS score in patients with PPPD, in patients with other vestibular disorders and in control subjects(24 months)
  • Measurement of the DHI score in patients with PPPD, patients with other vestibular disorders and control subjects(24 months)

研究者

发起方
Hôpital Européen Marseille
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验