Tokyo, Sept. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000062726) titled 'Clinical impact of visualization of infant zones on prevalence of Methicillin-Resistant Staphylococcus aureus in the Neonatal Intensive Care Unit in Japan' on Sept. 1.
Study Type:
Interventional
Study Design:
Basic Design - Single arm
Randomization - Non-randomized
Blinding - Open -no one is blinded
Control - Historical
Primary Sponsor:
Institute - University of Shizuoka
Condition:
Condition - MRSA detection in Neonatal Intensive Care Units
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - This study aimed to assess the impact of visualizing patient zone-healthcare area boundaries on hand hygiene compliance and MRSA detection in Neonatal Intensive Care Units treating moderately to severely ill infants.
Basic objectives2 - Efficacy
Intervention:
Interventions/Control_1 - In the pre-intervention period (Before), no visual boundary indicators were present. In the intervention period (After), patient zone-healthcare area boundaries were marked using standardized visual cues (colored tape, floor lines, and signage).
Eligibility:
Age-lower limit - Not applicable
Age-upper limit - Not applicable
Gender - Male and Female
Key inclusion criteria - Neonatal Intensive Care Units designated as core facilities treating severely ill infants or designated facilities treating moderately ill infants (total of 297 facilities invited).
NICUs with an open- floor bed layout.
Facilities that obtained Infection Prevention and Control Fee I in fiscal year 2021.
Facilities that conduct routine active surveillance cultures for MRSA.
Key exclusion criteria - NICUs without an open-floor bed layout.
Facilities that did not obtain Infection Prevention and Control Fee I in fiscal year 2021.
Facilities that do not conduct routine active surveillance cultures for MRSA.
NICUs unable to provide pre-intervention and post-intervention data required for outcome assessment.
Facilities that declined participation or were unable to implement standardized visual boundary markers.
Target Size - 15
Recruitment Status:
Recruitment status - Completed
Date of protocol fixation - 2022 Year 04 Month 21 Day
Date of IRB - 2022 Year 05 Month 06 Day
Anticipated trial start date - 2022 Year 07 Month 01 Day
Last follow-up date - 2023 Year 12 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000069579
Disclaimer: Curated by HT Syndication.