Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05402280

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

University of Ostrava

Ostrava, Česká Republika, Czechia, 70300

Actively Recruiting

Loading map...

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here