- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01822158
Vaginal Delivery Debrief Checklist to Improve Team Communication (VDD)
April 2, 2019 updated by: Providence Health & Services
Vaginal Delivery Debrief: A Nursing Research Study
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.
Study Overview
Status
Completed
Intervention / Treatment
Detailed 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.
Study Type
Interventional
Enrollment (Actual)
44
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Washington
-
Olympia, Washington, United States, 98506
- Providence St Peter Hospital 413 Lilly RD NE
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
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:
- None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: vaginal delivery debrief checklist
Utilization of a Vaginal Delivery Debrief Checklist after vaginal deliveries for a period of three months, by team members who have consented to be a part of this study and who are present at vaginal deliveries.
The Vaginal Delivery Debrief checklist consists of 2 levels.
The first level includes a list of 6 key elements, such as APGAR scores,estimated blood loss, perineal repair, etc.
The second level,or extended debrief, occurs whenever unanticipated outcomes, such as low APGAR scores, postpartum hemorrhage or a difficult delivery occurs.
Team members complete the checklist after each delivery they attend.
|
Participating team members will utilize Vaginal Delivery Debrief checklist
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Determine if there is a change in satisfaction with team communication following the use of a structured debrief checklist after vaginal deliveries.
Time Frame: Within 6 months of data collection
|
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.
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Within 6 months of data collection
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Determine if the use of a vaginal delivery debrief checklist will reduce documentation of conflicting data in the electronic medical record.
Time Frame: Within 6 months of data collection
|
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.
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Within 6 months of data collection
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Daren B Sachet, RN, BSN, MPA, Providence Health & Services
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 12, 2013
Primary Completion (Actual)
October 31, 2013
Study Completion (Actual)
December 31, 2013
Study Registration Dates
First Submitted
March 20, 2013
First Submitted That Met QC Criteria
April 1, 2013
First Posted (Estimate)
April 2, 2013
Study Record Updates
Last Update Posted (Actual)
April 4, 2019
Last Update Submitted That Met QC Criteria
April 2, 2019
Last Verified
March 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PHS PSPH N 002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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