Impact of ERCS on Perceived Stress in Patients Hospitalized in the Post-resuscitation Rehabilitation Service
Recruiting
N/A
Interventional Study
Stress Disorders, Post-Traumatic
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
- Other
- Participants needed
- 38 (estimated)
- Sponsor
- Hôpital Européen Marseille · Other
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About This Trial
Surviving an intensive care unit hospitalization (ICU) can be the beginning of a long rehabilitation journey, hindered by symptoms of stress, PTSD, anxiety, and depression. In order to improve the care of these patients, it's essential to explore effective non-pharmacological approaches to reduce stress. Many non-drug techniques are being developed to alleviate the physical and psychological pain …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Aged ≥ 18 years
* Hospitalized adults in a Post-Intensive Care Rehabilitation Unit (SRPR)
* Having given free and informed written consent
Exclusion Criteria:
* Pregnant or breastfeeding woman
* Persons deprived of their liberty by a judicial or administrative decision.
* Pe…
Contacts