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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01822158
Other study ID # PHS PSPH N 002
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 12, 2013
Est. completion date December 31, 2013

Study information

Verified date March 2019
Source Providence Health & Services
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is to determine if using a standardized debrief checklist after vaginal delivery improves communication between the vaginal delivery health care team members and if using the checklist increases a sense of enhanced communication between team members.


Description:

This is a study for providers who are a part of the health care team involved with vaginal delivery of newborns. A checklist has been developed that may improve communication between team members following birth. The goal of this study is to evaluate whether the checklist improves or enhances team member communication.


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date December 31, 2013
Est. primary completion date October 31, 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Registered Nurses (RNs) and Licensed Practical Nurses (LPNs) in the Women's and Children's Services Department who attend vaginal deliveries as well as providers who attend vaginal deliveries at Providence St Peter Hospital Family Birth Center in Olympia Washington (WA).

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Vaginal Delivery Debrief Checklist
Participating team members will utilize Vaginal Delivery Debrief checklist

Locations

Country Name City State
United States Providence St Peter Hospital 413 Lilly RD NE Olympia Washington

Sponsors (1)

Lead Sponsor Collaborator
Providence Health & Services

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Determine if there is a change in satisfaction with team communication following the use of a structured debrief checklist after vaginal deliveries. An electronic opinion survey will be administered to participants both pre and post checklist utilization. The survey was derived from communication literature on medical teams such as the collaboration items and 3 subscales from the labour and delivery version of the Safety Attitudes Questionnaire (SAQ) and the Agency for Healthcare Research and Quality (AHRQ) TeamSTEPPS training program for high functioning medical teams. Within 6 months of data collection
Secondary Determine if the use of a vaginal delivery debrief checklist will reduce documentation of conflicting data in the electronic medical record. Utilizing the pre-validated Vaginal Delivery Debrief Medical Record Audit Tool, records will be examined pre and post use of the Vaginal Delivery Debrief Checklist. Assessment will be made to determine if there are fewer conflicting data points in the electronic medical record (EMR) for key elements following use of the Vaginal Delivery Debrief Checklist. Within 6 months of data collection