Effects of an Integrated Sleep Promotion Bundle on Sleep Quality and Delirium in Trauma Intensive Care Unit Patients

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0011718

Enrollment

Registered

2026-03-12

Start date

2026-03-16

Completion date

Unknown

Last updated

2026-03-16

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

Conditions

None listed

Interventions

Behavioral : 1. Control Group The control group receives routine care according to the standard nursing protocols of the trauma intensive care unit (TICU). To induce sleep, room lights and televisions

the intervention is considered successfully implemented if the participant remains asleep. (2) Light Management Room lights are

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1) Adults aged 18 years or older. (2) Patients admitted to the Trauma Intensive Care Unit (TICU) due to trauma. (3) Hemodynamically stable patients (minimal use of vasopressors and MAP >65mmHg). (4) Patients with a Richmond Agitation-Sedation Scale (RASS) score between -1 and +1 who are capable of communication. (5) Individuals who fully understand the study's purpose and procedures and provide voluntary informed consent to participate.

Exclusion criteria

Exclusion criteria: (1) Patients diagnosed with and undergoing treatment for pre-existing sleep disorders (e.g., narcolepsy, insomnia, or severe sleep apnea) prior to admission. (2) Patients for whom active treatment is deemed futile due to imminent death (end-of-life care). (3) Patients unable to wear a commercial wearable activity tracker due to physical conditions such as quadriplegia or limb amputation. (4) Patients who refuse or are unable to wear sleep aids (e.g., earplugs, sleep masks). (5) Patients whose TICU stay is less than 72 hours. (6) Individuals with photosensitive epilepsy or those within 3 months following retinal surgery.

Design outcomes

Primary

Measure	Time frame
Korean version of Richmond Campbell Sleep Questionnaire;Korean version of the Confusion Assessment Method for the Intensive Care Unit;Objective sleep parameters, including total sleep time (TST), sleep efficiency (SE), and wake after sleep onset (WASO), are measured using a wearable activity tracker (Fitbit).	—

Countries

Korea, Republic of

Contacts

Public ContactYunkag LEE

Armed Forces Capital Hospital

lsyk8c@gmail.com+82-31-789-2850

Outcome results