The SBAR Effect on Safety Attitudes in the Perinatal Department

This study has been completed.

Sponsor:

Information provided by (Responsible Party):

Sheng-Mou Hsiao, Far Eastern Memorial Hospital

ClinicalTrials.gov Identifier:

NCT01570335

First received: April 2, 2012

Last updated: March 8, 2013

Last verified: March 2013

Purpose

The aim of this study is to analyze the impact of SBAR by the SAQ questionnaire in the perinatal department.

Condition
Fetal Distress

Study Type:	Observational
Study Design:	Observational Model: Cohort Time Perspective: Cross-Sectional

Further study details as provided by Far Eastern Memorial Hospital:

Primary Outcome Measures:

Changes of patient safety attitude after introducing SBAR [ Time Frame: 6 month ] [ Designated as safety issue: No ]
Changes of patient safety attitude after introducing SBAR in the perinatal ward

Enrollment:	40
Study Start Date:	April 2012
Study Completion Date:	March 2013
Primary Completion Date:	March 2013 (Final data collection date for primary outcome measure)

Eligibility

Study Population

All Physicians and Nurses in the Perinatal Department

Criteria

Inclusion Criteria:

Exclusion Criteria:

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT01570335

Locations

Taiwan
Far Eastern Memorial Hospital
Banqiao, New Taipei, Taiwan, 22050

Sponsors and Collaborators

Far Eastern Memorial Hospital

More Information

No publications provided

Responsible Party:	Sheng-Mou Hsiao, Chief, Department of Obstetrics & Gynecology, Far Eastern Memorial Hospital
ClinicalTrials.gov Identifier:	NCT01570335 History of Changes
Other Study ID Numbers:	101010-E
Study First Received:	April 2, 2012
Last Updated:	March 8, 2013
Health Authority:	Taiwan: Institutional Review Board

Keywords provided by Far Eastern Memorial Hospital:

SBAR,
SAQ,
Team Resource Management

Additional relevant MeSH terms:

Fetal Distress
Signs and Symptoms

ClinicalTrials.gov processed this record on June 17, 2013