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临床试验/NCT02792738
NCT02792738已完成不适用

Effect of Hypnosis on Dyspnea

Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2016年5月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20
试验地点
2
主要终点
Subject rating of Breathing Discomfort (affective component of dyspnea)

研究概览

简要总结

The purpose of this protocol is to test the effect of hypnosis on laboratory dyspnea.

详细描述

This is a study of permissive suggestion in two laboratory models of dyspnea ("work/effort", "air hunger"). Breathing discomfort rating induced by laboratory models of dyspnea will be assessed before, during and after hypnosis.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

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

  • healthy volunteers

排除标准

  • pregnancy
  • ongoing pain
  • respiratory disease
  • high levels of depression, panic disorder, or other significant mental health problems
  • not fluent in french

研究组 & 干预措施

hypnosis, visual distraction

Experimental

This is a crossover study in which each subject will be exposed to a 5 min phase of hypnotic suggestion and visual distraction.

For hypnotic suggestion, subject will be invited to experience a pleasant memory . Indirect and permissive suggestion will be used.

For visual distraction, subject will be watching the movie "la marche des empereurs"

干预措施: hypnosis (Behavioral)

结局指标

主要结局

Subject rating of Breathing Discomfort (affective component of dyspnea)

时间窗: continuous measurement for 5 minutes

Subjects will rate breathing discomfort using a visual analog scale at baseline (pre-intervention), during the intervention (hypnosis/ visual distraction) and after intervention (recovery) while subject will be submitted to the laboratory model of dyspnea for 5 minutes (three runs of laboratory dyspnea (baseline, intervention and recovery).

Subject rating of dyspnea intensity (sensory component of dyspnea)

时间窗: continuous measurement for 5 minutes

Subjects will rate dyspnea intensity using a visual analog scale at baseline (pre-intervention), during the intervention (hypnosis/ visual distraction) and after intervention (recovery) while subject will be submitted to the laboratory model of dyspnea for 5 minutes (three runs of laboratory dyspnea (baseline, intervention and recovery).

次要结局

未报告次要终点

研究者

发起方
Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil
申办方类型
Other
责任方
Sponsor

研究点 (2)

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