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Environmental Intervention on Delirious Patients

The Effect of Environmental Intervention on Critically-ill Surgical Patients With Delirium

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04042649
Enrollment
192
Registered
2019-08-02
Start date
2013-06-01
Completion date
2014-10-31
Last updated
2019-08-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delirium

Keywords

intensive care unit, critically ill patients, environmental intervention

Brief summary

The implementation of environmental intervention program reduced the duration of delirium and length of stay at the ICU in critically-ill surgical patients.

Detailed description

Purpose: Delirium occurs among patients in intensive care unit at high rates and increases the risk for morbidity and mortality. The purpose of this study is to investigate the effects of environmental interventions for the prevention of delirium. Methods: A total of 192 patients who had been admitted to the surgical intensive care unit (SICU) in Asan Medical Center during the pre-intervention period (Jun 2013 to Oct 2013) and the post-intervention period (Jun 2014 to Oct 2014) was enrolled and prospective cohort study was done. The environmental intervention included cognitive assessment, providing orientation and comfortable environment, and a proper sleeping environment. The primary outcomes were the incidence rate of delirium, time of delirium onset, and the duration of delirium.

Interventions

provide environmental intervention (help sleep cycle, provide comfortable environment)

Sponsors

Asan Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* with an age of 18 years or older * who understood the purpose of this study and agreed to participate * stayed in the SICU for a period of 48 hours or longer

Exclusion criteria

* who remained unresponsive \[defined as the Richmond Agitation-Sedation Scale (RASS) less than -4\] * who could not measure Confusion Assessment Method (CAM-ICU) due to severe visual or hearing disturbance * who had a history of severe psychiatric or neurologic deficit * who required an isolation room due to transplantation or immunologic compromise * who were discharged from ICU within 48 hours * who were re-admitted to the ICU * who were less than 18 years old * who were admitted to the Surgical ICU through another ICU

Design outcomes

Primary

MeasureTime frame
the duration of delirium5 month
the incidence rate of delirium5 month
time to delirium onset5 month

Secondary

MeasureTime frame
the rate of re-admission to the SICU5 month
the number of days of ventilator use5 month
mortality rate.5 month
the length of stay at the SICU5 month
the length of stay at hospital5 month

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026