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.
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