Ireland
--:--IST
Recruiting Not applicable

Sleep Disturbances and Delirium

NCT05402280 · tracked via the Priya Life Science Czechia tracker
Phase
Not applicable
Started
2022-05-01
Last updated
2025-02-25

Condition(s) studied

Sleep Disturbance

Investigational drug(s) / intervention(s)

Sleep protocol

Sleep protocol: To investigate the effect of a multicomponent sleep protocol on the quality of sleep hospitalized patients assessed both subjectively and objectively.

Study summary

Delirium is a frequent and serious problem in hospitalized patients; it is associated with multiple hospital-acquired complications. There is evidence that the incidence of deliri-um may be minimized by multimodal interventions (pain management, shortening the duration of mechanical ventilation, light sedation, avoiding benzodiazepines, routine delirium monitoring, and early mobilization). Even though a clear association between sleep and delirium has not been established, many studies suggest that sleep disturban-ces may be a key risk factor for the development of delirium. Therefore, sleep promoti-on is becoming an integral part of clinical care. The project support the hypothesis that non-pharmacological preventive interventions promoting sleep (sleep protocol) positive-ly influence the quality of sleep and reduce the incidence of delirium in hospitalized patients. This will be verified by qualitative and quantitative research methods, with the quantitative study being divided into three prospective cross-sectional studies and one interventional study. Data will be obtained from 3240 hospitalized patients by combi-ning subjective methods (questionnaire surveys) and objective measurements (acti-graphy). The project outcomes will allow better understanding of the relationship betwe-en sleep and delirium. A set of non-pharmacological preventive interventions promoting sleep will be developed, with a subsidiary aim to potentially reduce the incidence of delirium in hospitalized patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * age over 18 years * a hospital stay longer than 24 hours * a hospital stay longer than 36 hours * hospitalized for at least 72 hours, without previous sleep disturbances, without cognitive impairment Exclusion Criteria: * Patients with cognitive impairment preventing them from cooperating * Glasgow Coma Scale score below 12 * terminal disease * previous and current treatment for sleep disturbances * neurocognitive dysfunction (dementia) * sedative administration over the last 24 hours

Primary outcome measure(s)

  • Change quality of sleep during hospitalization (subjectively and objectively) — 25 months
    Assessment of quality of sleep using Richards Campbell Sleep Questionnaire (RCSQ) five-item visual analogue scale was designed as an outcome measure for assessing the perception of sleep in patients. The RCSQ contains 5 items (sleep depth, sleep latency, awakenings, returning to sleep and sleep quality) plus noise as an optional item (evaluated separately). Each item is scored by using a 0-100 visual analogue scale. The total score is calculated as the mean of all items, with 0 and 100 representing the worst and best sleep, respectively. Objectively sleep were assed by actigraphy -the method collects and stores data generated by patient movements.

Trial sites (1)

FacilityCityRegionStatus
University of Ostrava Ostrava Česká Republika Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05402280 on ClinicalTrials.gov ↗ ← All trials in Czechia