Sleep for Inpatients: Empowering Staff to Act (SIESTA)
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|ClinicalTrials.gov Identifier: NCT02025959|
Recruitment Status : Recruiting
First Posted : January 1, 2014
Last Update Posted : October 1, 2019
Getting better sleep in the hospital is especially important due to a variety of adverse health effects that can potentially worsen patient recovery.
To address these concerns and improve sleep in US hospitals, we aim to develop the SIESTA (Sleep for Inpatients: Empowering Staff to Act) program as an educational intervention designed to prepare hospital staff to assist patients in obtaining better sleep in hospitals and recognize the importance of screening for sleep disorders. The major educational goals of this proposal is to develop and pilot test an online educational program (SIESTA) which aims to train and motivate medical professionals to provide better sleep for hospitalized patients.
We will utilize data from an ongoing sleep study, performed by the research team at the University of Chicago that looks at how adult patients are able to sleep while they are in the hospital, as a means of education for the participating medical staff.
|Condition or disease||Intervention/treatment||Phase|
|Sleep Disorders Sleep||Behavioral: Educating hospital staff on good sleep hygiene for patients and screening for sleep disorders||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||300 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Health Services Research|
|Official Title:||Sleep for Inpatients: Empowering Staff to Act|
|Study Start Date :||August 2013|
|Estimated Primary Completion Date :||August 2020|
|Estimated Study Completion Date :||August 2020|
Experimental: Educational Intervention
Educating hospital staff on good sleep hygiene for patients and screening for sleep disorders
Behavioral: Educating hospital staff on good sleep hygiene for patients and screening for sleep disorders
- Impact of Educational program [ Time Frame: Four years ]We will assess if the SIESTA program translates into behavior change based on staff satisfaction, knowledge, behavior and qualitative analysis.
- Patient Outcomes [ Time Frame: Four Years ]We will asses affect of Intervention on hospitalized patient outcomes.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02025959
|Contact: Samantha Anderson, BAfirstname.lastname@example.org|
|United States, Illinois|
|University of Chicago Medical Center||Recruiting|
|Chicago, Illinois, United States, 60637|
|Contact: Lisa M Spampinato, BS 773-459-4879 email@example.com|
|Principal Investigator: Vineet M Arora, MD, MAPP|
|Principal Investigator:||Vineet M Arora, MD, MAPP||University of Chicago|