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Family Involvement in ICU

I

Istanbul University - Cerrahpasa

Status

Enrolling

Conditions

Delirium in the Intensive Care Unit
Family
Relatives
Sedatives
Intensive Care Patients

Study type

Observational

Funder types

Other

Identifiers

NCT06770751
2024/231

Details and patient eligibility

About

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?

Enrollment

122 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

122 participants in 2 patient groups

Short involvement of family
Description:
A group where relatives spend up to 2 hours with patients and are involved in their care.
Long involvement of family
Description:
A group where relatives spend more than 2 hours with patients and are involved in their care.

Trial contacts and locations

1

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Central trial contact

Oguzhan Kayhan

Data sourced from clinicaltrials.gov

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