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Recruiting NCT06770751

NCT06770751 Family Involvement in ICU

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Clinical Trial Summary
NCT ID NCT06770751
Status Recruiting
Phase
Sponsor Istanbul University - Cerrahpasa
Condition Intensive Care Patients
Study Type OBSERVATIONAL
Enrollment 122 participants
Start Date 2025-01-13
Primary Completion 2025-06-30

Trial Parameters

Condition Intensive Care Patients
Sponsor Istanbul University - Cerrahpasa
Study Type OBSERVATIONAL
Phase N/A
Enrollment 122
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-01-13
Completion 2025-06-30

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Brief Summary

The aim of this prospective cohort study was to investigate the effect of the time spent with relatives of patients treated in a tertiary intensive care unit on patient outcomes. The main question it aimed to answer was: Does spending more time with relatives of patients in intensive care result in lower sedative agent requirements? Does spending more time with relatives of patients in intensive care result in less delirium, fewer ventilator days, and shorter ICU stays?

Eligibility Criteria

Inclusion Criteria: * Patients aged 18 and over. * Patients with at least one family member actively involved in the care process in the ICU. Exclusion Criteria: * Patients with pre-existing cognitive impairment or dementia. * Patients with severe traumatic brain injury. * Patients with an expected mortality in the ICU of more than 80%. * Absence of family members for patients admitted to the ICU.

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