Actively Recruiting
Sleep Disturbances and Delirium
Led by University of Ostrava · Updated on 2025-02-25
3240
Participants Needed
1
Research Sites
191 weeks
Total Duration
On this page
Sponsors
U
University of Ostrava
Lead Sponsor
U
University Hospital Ostrava
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Sleep Disturbances and Delirium
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years
- Hospital stay longer than 24 hours
- Hospital stay longer than 36 hours
- Hospitalized for at least 72 hours without previous sleep disturbances or cognitive impairment
You will not qualify if you...
- Cognitive impairment preventing cooperation
- Glasgow Coma Scale score below 12
- Terminal disease
- Previous or current treatment for sleep disturbances
- Neurocognitive dysfunction such as dementia
- Sedative use within the last 24 hours
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University of Ostrava
Ostrava, Česká Republika, Czechia, 70300
Actively Recruiting
Research Team
M
Michaela Rybova
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
NON_RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
4
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