For Healthcare Professionals

Sleep Disturbances and Delirium

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About the study

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.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:

  1. age over 18 years
  2. a hospital stay longer than 24 hours
  3. a hospital stay longer than 36 hours
  4. hospitalized for at least 72 hours, without previous sleep disturbances, without cognitive impairment

EXCLUSION CRITERIA

Exclusion Criteria:

  1. Patients with cognitive impairment preventing them from cooperating
  2. Glasgow Coma Scale score below 12
  3. terminal disease
  4. previous and current treatment for sleep disturbances
  5. neurocognitive dysfunction (dementia)
  6. sedative administration over the last 24 hours
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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall +420608714997Email iconEmail Study Center

Study Details


Contition

Sleep Disturbance

Age

18+

Phase

NA

Participants Needed

3240

Est. Completion Date

Dec 31, 2025

Treatment Type

INTERVENTIONAL


Sponsor

University of Ostrava

ClinicalTrials.gov NCT Identifier

NCT05402280

Study Number

SLEEP

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