The SBAR Effect on Safety Attitudes in the Perinatal Department

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

Completed

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Key information

Conditions

Fetal Distress Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

20 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Far Eastern Memorial Hospital

Banqiao District, New Taipei, 22050, Taiwan

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

All Physicians and Nurses in the Perinatal Department

Exclusion criteria

Treatment and study plan

Primary outcomes

Changes of patient safety attitude after introducing SBAR

Time frame: 6 month

Changes of patient safety attitude after introducing SBAR in the perinatal ward

Sponsors and collaborators

Lead sponsor

Far Eastern Memorial Hospital

Other

Registry information

Important dates

Study start: 2012
Primary completion: 2013
Study completion: 2013
First posted: Apr 4, 2012
Registry last updated: Dec 3, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed