Post-traumatic stress disorder induced by dyspnea Mental and Behavioural Disorders Post-traumatic stress disorder
Conditions
Interventions
Current intervention as of 30/12/2021:
Experimental induced dyspnea and questionnaires (mood and psychological aspects)
Observational study :
- duration of participation for a subject : 3 months
- du
Sponsors
Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil
Eligibility
Sex/Gender
All
Age
18 Years to 110 Years
Inclusion criteria
Inclusion criteria: Aged 18 years or over
Exclusion criteria
Exclusion criteria: 1. Pregnant 2. Protected adult 3. Person deprived of liberty 4. Existing respiratory pathology 5. Existence of any chronic pathology identified and subject to treatment, including psychiatric disorders 6. Absence of affiliation to social security 7. Vulnerable
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Current primary outcome measure as of 30/12/2021: Presence of post-traumatic stress disorder, assessed with the validated French version of the PCL-5 questionnaire (score >38), 3 months after the experiment _____ Previous primary outcome measure: Presence of post-traumatic stress disorder, assessed with the validated French version of the PCL-5 questionnaire (score >38), 4 weeks after the experiment. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Change in "state anxiety" (STAI A questionnaire) compared with baseline (online, 1 week and 4 weeks after the experiment) 2. Correlation between score using Peritraumatic Distress Inventory (PDI) and score using PCL-5, 4 weeks after the experiment (added 30/09/2020) 3. Persistence of a psychological impact (bad memories, negative emotions, nightmares) 7 days after the last experiment using a semi-structured interview | — |
Countries
France
Contacts
Public ContactSophie Lavault
Outcome results
None listed