Vaginal Delivery Debrief Checklist to Improve Team Communication (VDD)
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT01822158|
Recruitment Status : Unknown
Verified May 2013 by Providence Health & Services.
Recruitment status was: Enrolling by invitation
First Posted : April 2, 2013
Last Update Posted : May 22, 2013
|Condition or disease||Intervention/treatment|
|Other Specified Complications of Labor and Delivery||Other: Vaginal Delivery Debrief Checklist|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||100 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Vaginal Delivery Debrief: A Nursing Research Study|
|Study Start Date :||May 2013|
|Estimated Primary Completion Date :||October 2013|
|Estimated Study Completion Date :||December 2013|
Experimental: 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.
Other: Vaginal Delivery Debrief Checklist
Participating team members will utilize Vaginal Delivery Debrief checklist
- 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.
- 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.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01822158
|United States, Washington|
|Providence St Peter Hospital 413 Lilly RD NE|
|Olympia, Washington, United States, 98506|
|Principal Investigator:||Daren B Sachet, RN, BSN, MPA||Providence Health & Services|