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NCT01570335 Clinical Trial

The SBAR Effect on Safety Attitudes in the Perinatal Department

Fetal Distress Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01570335
Other study ID # 101010-E
Secondary ID
Status Completed
Phase N/A
First received April 2, 2012
Last updated December 1, 2015
Start date April 2012
Est. completion date March 2013

Study information
Verified date March 2013
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Institutional Review Board
Study type Observational

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date March 2013
Est. primary completion date March 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

- All Physicians and Nurses in the Perinatal Department

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Locations
Country Name City State
Taiwan Far Eastern Memorial Hospital Banqiao New Taipei

Sponsors (1)
Lead Sponsor Collaborator
Far Eastern Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Changes of patient safety attitude after introducing SBAR Changes of patient safety attitude after introducing SBAR in the perinatal ward 6 month No
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