Reported Experience Measurement on Reducing Patient Discomfort in Intensive Care

Recruiting N/A Interventional Study
PTSD - Post Traumatic Stress Disorder
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Health Services Research
Participants needed
1,242 (estimated)
Sponsor
Almaviva Sante · Other
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About This Trial
Hospitalisation in intensive care is always traumatic and can lead to a long rehabilitation process, slowed down by symptoms of anxiety and/or depression, and/or post-traumatic stress disorder (PTSD). These psychiatric disorders, or post-intensive care syndrome (PICS), can persist for several years after hospitalisation in intensive care and cause functional disability. They are associated with th…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patient, male or female, aged ≥ 18 years * Patient discharged alive from intensive care * Patient hospitalised in intensive care for at least three calendar days * Patient affiliated with or beneficiary of a social security scheme * Patient who speaks French and has signed an …
Contacts

Pierre KALFON, MD

+ 33 6 38 39 24 18

pierrekalfon@sfr.fr

CONTACT