SIESTA: Sleep for Inpatients: Empowering Staff to Act

Sponsor
University of Chicago (Other)
Overall Status
Recruiting
CT.gov ID
NCT02025959
Collaborator
(none)
300
1
1
108
2.8

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Educating hospital staff on good sleep hygiene for patients and screening for sleep disorders
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
N/A
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 :
Aug 1, 2013
Anticipated Primary Completion Date :
Aug 1, 2022
Anticipated Study Completion Date :
Aug 1, 2022

Arms and Interventions

Arm Intervention/Treatment
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

Outcome Measures

Primary Outcome Measures

  1. Impact of Educational program [Four years]

    We will assess if the SIESTA program translates into behavior change based on staff satisfaction, knowledge, behavior and qualitative analysis.

Secondary Outcome Measures

  1. Patient Outcomes [Four Years]

    We will asses affect of Intervention on hospitalized patient outcomes.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Chicago Medical Center Chicago Illinois United States 60637

Sponsors and Collaborators

  • University of Chicago

Investigators

  • Principal Investigator: Vineet M Arora, MD, MAPP, University of Chicago

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Chicago
ClinicalTrials.gov Identifier:
NCT02025959
Other Study ID Numbers:
  • 12-1766
First Posted:
Jan 1, 2014
Last Update Posted:
May 17, 2021
Last Verified:
May 1, 2021
Keywords provided by University of Chicago
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 17, 2021