Sleep Iniciation and Mantainance Disturbs
Conditions
Interventions
Observational cross-over trial, with 30 patients. A BIS sensor (Covidien IIc, Mainsfield, United States of America) will be attached to the forehead of the patients, to register sleep pattern in two c
Device
Sponsors
Hospital de Clínicas da Universidade Federal do Paraná
Instituto de Tecnologia para o Desenvolvimento - Lactec
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Adult and elderly critically ill individuals; admitted at the intensive care unit 2 of the Hospital de Clínicas da Universidade Federal do Paraná; with mild and moderate gravity diseases; with perspective of spending the next night at that unit; and that are able to understand and accept the terms of the Informed Consent.
Exclusion criteria
Exclusion criteria: Individuals with severe organ disfunction; wich compromise the comprehension and acceptance of the terms of the Informed Consent; individual who don't accept these terms; those identified as delirious; those who decide to leave the study after the inclusion. Individuals may decline participation at any time independently of justification.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Statistically significant increase in duration of slow wave sleep in nights preceded by bed bath, in comparison with nights not preceded by bed bath, considering the affered Bispectral Index®. This outcome will be verified after the second night of aferitions. | — |
Secondary
| Measure | Time frame |
|---|---|
| First secondary outcome: Increase in the duration of the profound sleep in nights preceded by bed bath occur independently of the confusion factors investigated: medication; pain; noise and luminosity. This outcome will be verified after the second night of aferitions, through analisys of the Bispectral Index®.;Second secondary outcome: Temperature evolution (central and cutaneous) on nights non preceded by bed bath and nights preceded by bed bath; measured with a tympanic thermometer and miniaturized thermal sensors. This outcome will be verified after the second night of aferitions. | — |
Countries
Brazil
Contacts
Public ContactRodolfo Pedrão
Hospital de Clínicas da Universidade Federal do Paraná
Outcome results
None listed