Delirium Clinical Trials

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Effect of a Triple Sleep-Promotion Protocol on Delirium Incidence in Intensive Care Units: A Multicenter Stratified Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Delirium is a common complication in intensive care units (ICUs) and may be associated with sleep disruption and frequent nighttime disturbances. This randomized controlled trial will evaluate whether a multicomponent nighttime sleep-promotion intervention, called the Triple Sleep-Promotion Protocol, can reduce the occurrence of new-onset delirium in adult ICU patients. The study is being conducted in four ICUs in Türkiye. Eligible patients who do not have delirium at the beginning of the study will be randomly assigned to either the intervention group or the control group. The intervention includes clustering nighttime nursing care, offering an eye mask and earplugs during protected sleep periods, and reducing avoidable nighttime light and noise whenever clinically feasible. Patients in the control group will receive usual ICU care. Patient safety and clinically necessary care will take priority over all sleep-promotion procedures. Participants will be followed during their ICU stay for up to five days. Delirium will be assessed twice daily using the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU). Nighttime sleep quality will also be assessed each morning using the Richards-Campbell Sleep Questionnaire. The primary aim is to determine whether the Triple Sleep-Promotion Protocol reduces the incidence of new-onset delirium compared with usual ICU care.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age 18 years or older. Admitted to one of the participating intensive care units. Expected ICU stay of at least 24 hours. Richmond Agitation-Sedation Scale (RASS) score between -3 and +4 at baseline. Negative Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) assessment at baseline.

⁃ Able to communicate in Turkish when communication is required for study assessments.

⁃ Written informed consent provided by the patient or, when the patient is unable to provide consent because of their clinical condition, by a first-degree relative.

Locations
Other Locations
Turkey
Çanakkale Onsekiz Mart University, Faculty of Health Sciences
RECRUITING
Çanakkale
Contact Information
Primary
Naile Alankaya, Assosiate Prof. PhD
naile.alankaya@gmail.com
+905334256510
Backup
Sevda Ateş
naile.alankaya@gmail.com
Time Frame
Start Date: 2026-08-15
Estimated Completion Date: 2027-03
Participants
Target number of participants: 200
Treatments
No_intervention: Usual ICU Care
Participants assigned to this arm receive usual ICU care according to the routine practices of the participating ICU. No study-specific nighttime care clustering, eye mask, earplugs, or structured reduction of nighttime light and noise is provided as part of the study. All routine clinical monitoring, nursing care, and medically necessary procedures continue according to standard ICU practice.
Experimental: Triple Sleep-Promotion Protocol
Participants assigned to this arm receive the Triple Sleep-Promotion Protocol in addition to usual ICU care. The protocol includes clustering nighttime nursing care, offering an eye mask and earplugs during designated protected sleep periods, and reducing avoidable nighttime light and noise whenever clinically feasible. The intervention is implemented during the nighttime period, approximately 22:00-08:00. Urgent or clinically necessary care, monitoring, and patient safety requirements take priority over all sleep-promotion procedures.
Related Therapeutic Areas
Sponsors
Leads: Naile ALANKAYA

This content was sourced from clinicaltrials.gov