Sleep Promotion for patients undergoing Heart Disease Treatment: randomized clinical trial
Not Applicable
- Conditions
- Sleep Hygiene
- Registration Number
- RBR-2pcycpx
- Lead Sponsor
- niversidade de São Paulo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Age over 18 years, communication and comprehension skills preserved.
Exclusion Criteria
Report of severe sleep disorder requiring daily treatment before hospitalization, such as sleep apnea, narcolepsy and chronic insomnia; presence of serious complication (aortic dissection, bleeding or stroke after the procedure) related to the treatment; presence of delirium as medical record evaluation; severe hearing and visual loss; history of neurological disease or diagnosed psychiatric disorders; admission to the Intensive Care Unit between 9:00 pm to 6:00 am after the percutaneous intervention procedure; treatment with mechanical ventilation; need for sedation during stay in the ICU, who are not fluent in the Portuguese language.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the quality of sleep of the participants in the control and intervention groups measured by the instruments after applying the intervention daily during their stay in the ICU. Participants in the intervention group are expected to have higher sleep quality scores
- Secondary Outcome Measures
Name Time Method The daytime sleepiness of the participants in the intervention group is expected to have lower scores according to the specific assessment instrument;The incidence of delirium is expected to be lower in the intervention group measured by the specific instrument.