Pilot Study of a Multidisciplinary Intervention in ICU Survivors At Risk for Psychological or Physical Morbidity
Recruiting
N/A
Interventional Study
Post-Intensive Care Syndrome
Depressive Symptoms
Anxiety
Physical Disability
Posttraumatic Stress Symptom
Critical Care, Intensive Care
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
- Prevention
- Participants needed
- 60 (estimated)
- Sponsor
- Region Stockholm · Government
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About This Trial
Pilot study of the feasibility and utility of an early, in-hospital multidisciplinary intervention in ICU survivors at risk for psychological and physical problems post-ICU stay
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
\- Patients admitted ≥12 hours to the ICU with an increased risk for physical or psychological sequelae (assessed with the PROGRESS-ICU/PREPICS instruments)
Exclusion Criteria:
* Dementia or other major cognitive problems
* Structural brain or spinal cord injury
* Multiple lim…
Contacts