Ignite Creation Date:
2024-05-06 @ 3:32 PM
Last Modification Date:
2024-10-26 @ 1:51 PM
Study NCT ID:
NCT04665505
Status:
NOT_YET_RECRUITING
Last Update Posted:
2023-12-05
First Post:
2020-11-10
Brief Title:
Resource Optimization in the Intensive Care Unit Setting
Sponsor:
Ottawa Hospital Research Institute
Organization:
Ottawa Hospital Research Institute
Study Overview
Official Title:
Resource Optimization in the Intensive Care Unit Setting A Staff Education and Scheduling Pilot Study to Improve Treatment Decisions and Staff Satisfaction
Status:
NOT_YET_RECRUITING
Status Verified Date:
2023-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of the study is to facilitate cost-effective high quality care within the the ICUs of two Ottawa teaching hospitals through educational workshops and nurse scheduling optimization
Detailed Description:
This intervention pilot study has been developed for Intensive Care Unit ICU physicians and nurses by the Resource Optimization Network RON for implementation in The Ottawa Hospital TOH Civic Campus and the Montfort Hospital The intervention targets ICU staff and is designed to reduce overall costs associated with ICU health care service delivery and improve staff satisfaction through reducing stress and associated burnout without sacrificing quality of care and patient outcomes The intervention involves two components that a build ICU staffs ie physicians and nurses knowledge to facilitate cost-effective and evidence-based decision making about patient care including tests treatments and procedures and b optimize nurse scheduling to ensure the presence of the appropriate number of nurses per shift thereby reducing stress burnout and limiting the need for overtime To evaluate the impact of the intervention a prepost-intervention design will be employed with a 3-month pre-intervention period followed by a 6-month intervention period and a 3-month post-intervention period
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None