Actively Recruiting

Age: 18Years +
All Genders
ID06770751

Family Involvement in the Intensive Care Unit A Prospective Study on Effects on Sedation, Delirium, Ventilator Use, and Length of Stay

Led by Istanbul University - Cerrahpasa · Updated on 2025-01-17

122

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to explore how spending time with family members affects patients treated in a tertiary intensive care unit (ICU). It focuses on whether increased family involvement can reduce the need for sedative medications, lower the occurrence of delirium, decrease the number of days on a ventilator, and shorten the length of ICU stays. The study examines these patient outcomes in a real-world ICU setting. Participants are adult ICU patients who have at least one family member actively involved in their care during their ICU stay. The study observes these patients prospectively, monitoring how time spent with relatives may influence sedation needs and other clinical outcomes. No specific treatment interventions are given, as this is an observational cohort study. During the study, each patient's sedative dose is recorded daily for up to the first four weeks in the ICU. Researchers will also assess delirium, ventilator usage, and length of ICU stay. Participation involves monitoring these health measures and family involvement without changing standard care. The study includes adult patients aged 18 and older and continues throughout their ICU admission as long as they remain eligible.

CONDITIONS

Official Title

Family Involvement in ICU

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 and over.
  • Patients with at least one family member actively involved in the care process in the ICU.
Not Eligible

You will not qualify if you...

  • 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.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Cerrahpaşa Medical Faculty

Istanbul, Turkey (Türkiye), 34153

Actively Recruiting

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Research Team

O

Oguzhan Kayhan

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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