Sleep for Inpatients: Empowering Staff to Act (SIESTA)
Primary Purpose
Sleep Disorders, Sleep
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Educating hospital staff on good sleep hygiene for patients and screening for sleep disorders
Sponsored by
About this trial
This is an interventional health services research trial for Sleep Disorders focused on measuring staff empowerment, Sleep Apnea, educational intervention
Eligibility Criteria
Inclusion Criteria:
- To be eligible to participate in this study, the subjects must be University of Chicago hospital employees over the age of 18 years old.
Exclusion Criteria:
- We will exclude any hospital staff under the age of 18 years old from this study as well as hospital patients and non-hospital staff.
Sites / Locations
- University of Chicago Medical CenterRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Educational Intervention
Arm Description
Educating hospital staff on good sleep hygiene for patients and screening for sleep disorders
Outcomes
Primary Outcome Measures
Impact of Educational program
We will assess if the SIESTA program translates into behavior change based on staff satisfaction, knowledge, behavior and qualitative analysis.
Secondary Outcome Measures
Patient Outcomes
We will asses affect of Intervention on hospitalized patient outcomes.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02025959
Brief Title
Sleep for Inpatients: Empowering Staff to Act
Acronym
SIESTA
Official Title
Sleep for Inpatients: Empowering Staff to Act
Study Type
Interventional
2. Study Status
Record Verification Date
May 2021
Overall Recruitment Status
Unknown status
Study Start Date
August 2013 (undefined)
Primary Completion Date
August 2022 (Anticipated)
Study Completion Date
August 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Chicago
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Disorders, Sleep
Keywords
staff empowerment, Sleep Apnea, educational intervention
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Educational Intervention
Arm Type
Experimental
Arm Description
Educating hospital staff on good sleep hygiene for patients and screening for sleep disorders
Intervention Type
Behavioral
Intervention Name(s)
Educating hospital staff on good sleep hygiene for patients and screening for sleep disorders
Primary Outcome Measure Information:
Title
Impact of Educational program
Description
We will assess if the SIESTA program translates into behavior change based on staff satisfaction, knowledge, behavior and qualitative analysis.
Time Frame
Four years
Secondary Outcome Measure Information:
Title
Patient Outcomes
Description
We will asses affect of Intervention on hospitalized patient outcomes.
Time Frame
Four Years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
To be eligible to participate in this study, the subjects must be University of Chicago hospital employees over the age of 18 years old.
Exclusion Criteria:
We will exclude any hospital staff under the age of 18 years old from this study as well as hospital patients and non-hospital staff.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Samantha Anderson, BA
Phone
773-834-8904
Email
sanderson7@medicine.bsd.uchicago.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vineet M Arora, MD, MAPP
Organizational Affiliation
University of Chicago
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Chicago Medical Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60637
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lisa M Spampinato, BS
Phone
773-459-4879
Email
lspampinato@medicine.bsd.uchicago.edu
First Name & Middle Initial & Last Name & Degree
Vineet M Arora, MD, MAPP
12. IPD Sharing Statement
Citations:
PubMed Identifier
25317085
Citation
Shear TC, Balachandran JS, Mokhlesi B, Spampinato LM, Knutson KL, Meltzer DO, Arora VM. Risk of sleep apnea in hospitalized older patients. J Clin Sleep Med. 2014 Oct 15;10(10):1061-6. doi: 10.5664/jcsm.4098.
Results Reference
result
Learn more about this trial
Sleep for Inpatients: Empowering Staff to Act
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