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NCT02792738 Clinical Trial

Effect of Hypnosis on Dyspnea

Healthy Clinical Trial

— Hypnopnee  

Official title:
Effect of Hypnosis on Dyspnea

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02792738
Other study ID # ADOREPS_3
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 23, 2016
Est. completion date September 13, 2016

Study information
Verified date September 2019
Source Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

Description:

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.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date September 13, 2016
Est. primary completion date September 13, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- healthy volunteers

Exclusion Criteria:

- pregnancy

- ongoing pain

- respiratory disease

- high levels of depression, panic disorder, or other significant mental health problems

- not fluent in french

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• hypnosis

Locations
Country Name City State
France Service de Pneumologie et Réanimation Médicale Paris

Sponsors (1)
Lead Sponsor Collaborator
Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Subject rating of Breathing Discomfort (affective component of dyspnea) 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). continuous measurement for 5 minutes
Primary Subject rating of dyspnea intensity (sensory component of dyspnea) 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). continuous measurement for 5 minutes
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