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Study identifier: NCT07525284 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Reported Experience Measurement on Reducing Patient Discomfort in Intensive Care

Condition: PTSD - Post Traumatic Stress Disorder  ·  Sponsor: Almaviva Sante

PhaseNA
Planned participants1242
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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 the use of psychotropic drugs and mental health services, and impair health-related quality of life. This research is based on the hypothesis that the traumatic nature of intensive care hospitalisation can be reduced by implementing programmes to improve intensive care hospitalisation conditions, promoting changes in the practices of all healthcare professionals involved in intensive care. IPREA3 study (Kalfon et al, 2017) demonstrated that implementation of a tailor-made, multi-component programme, led by a doctor/non-medical caregiver significantly reduced the overall discomfort score (derived from the IPREA questionnaire) perceived by patients hospitalised in an intensive care unit with sufficient experience in applying this programme, having used it for at least 5 months (Kalfon et al, 2017) . The originality and interest of this research, in comparison with the IPREA3 study, lie in the following aspects: * the use of the most recent version of the IPREA questionnaire, * the questionnaire was completed by the patient themselves without the intervention of a caregiver (self-admi…

This description comes directly from the study's public registry record.

Talk to the study team

Pierre KALFON, MD  ·  + 33 6 38 39 24 18  ·  pierrekalfon@sfr.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Hôpital Privé La CasamanceAubagne, France, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07525284