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Post Intensive Care Syndrome / Anxiety / Depressive Symptoms · Interventional Study
ClinicalTrials.gov · August 13, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a terminated pilot study registered on ClinicalTrials.gov with no published results in the registry record. The study aimed to assess feasibility and utility of a case-manager led multidisciplinary intervention for ICU survivors at risk for post-intensive care syndrome and psychological morbidity. No outcome data are available to evaluate clinical or operational effectiveness.
Interventional, Single Group, Open label, Prevention purpose. Post-Intensive Care Syndrome, Depressive Symptoms, Anxiety, Physical Disability, Posttraumatic Stress Symptom, Critical Care, Intensive Care; age from 18 Years. Intervention: Interventional arm. n = 41. 2 sites: Sweden.
This is a terminated pilot study registered on ClinicalTrials.gov with no published results in the registry record. The study aimed to assess feasibility and utility of a case-manager led multidisciplinary intervention for ICU survivors at risk for post-intensive care syndrome and psychological morbidity. No outcome data are available to evaluate clinical or operational effectiveness.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
This is a terminated pilot study with no posted results; the registry record describes planned feasibility and utility assessment only, without outcome data.
As stated by the source record.
Quoted from the source exactly as published.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT06118606). This is a study registration, not published results. Lead sponsor: Region Stockholm. Recruitment status: TERMINATED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 41 participants (ACTUAL). Conditions: Post-Intensive Care Syndrome, Depressive Symptoms, Anxiety, Physical Disability, Posttraumatic Stress Symptom, Critical Care, Intensive Care. Interventions: OTHER: Case-manager led multidisciplinary follow-up after intensive care. Primary outcome measures: Feasibility of the intervention , Outcome measured during and after termination of data collection and end of intervention; Utility of the intervention , Outcome measured three-four months after ICU discharge. Brief summary: 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
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.