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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03529214
Other study ID # IRB18-0550
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 29, 2018
Est. completion date December 31, 2019

Study information

Verified date March 2020
Source Harvard School of Public Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the feasibility of a pilot project to improve communication and teamwork and to increase vaginal delivery rates at hospital in the United States


Recruitment information / eligibility

Status Completed
Enrollment 5217
Est. completion date December 31, 2019
Est. primary completion date September 30, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Clinician Participant Inclusion Criteria:

- All clinicians who have practice privileges at a study site

Clinician Participant Exclusion Criteria:

- None

Implementation Team Participant Inclusion Criteria:

- Champions, super-users and others who have been involved in the implementation of "Team Birth Project" at a study site

Implementation Team Participant Exclusion Criteria:

- None

Patient Participant Inclusion Criteria:

- 18 years or older

- Live birth. Includes: spontaneous or induction of labor; Vaginally, with an instruments (forceps / vacuum), or unscheduled cesarean delivery

- Patient at a study site piloting "Team Birth Project"

Patient Participant Exclusion Criteria:

- Under 18 years old

- Scheduled cesarean delivery

- Experienced intrapartum, stillbirth, or neonatal death

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Exposed study site
The study sites will pilot the Team Birth Project designed to improve team communication (between providers, as well as providers and patients). The project includes three key implementation steps that involve: preparing local sites for the implementation of the project; training and coaching on the use of the tools; and sustainment through peer coaching and data feedback. A mixed methods approach will be used to assess acceptability and feasibility, including: (1) clinician surveys and interviews, (2) implementation team focus groups, and (3) patient surveys.

Locations

Country Name City State
United States Overlake Medical Center Bellevue Washington
United States EvergreenHealth Medical Center Kirkland Washington
United States Saint Francis Hospital Tulsa Oklahoma
United States South Shore Hospital Weymouth Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Harvard School of Public Health Brigham and Women's Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Acceptability to clinicians At the project midline, percent of clinicians (physicians, midwives, and nurses) who would definitely or probably recommend the Team Birth project tools for use in other labor and delivery units. The window begins on the 180th day to the 270th day from the start date at each site (180 days to 270 days). If clinicians complete more than one survey in the window, we will use the first one.
Primary Acceptability to patients At the project midline, percent of patients who definitely or somewhat had the role they wanted in making decisions about their labor, among patients who wanted to make collaborative decisions with clinicians. The window begins on the 180th day to the 270th day from the start date at each site (180 days to 270 days).
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