Program of Research for the Optimization of a Supervised Patient Pathway for Expectant According to Risk in Obstetrics

NACompletedINTERVENTIONAL
Enrollment

1,532

Participants

Timeline

Start Date

December 5, 2016

Primary Completion Date

July 31, 2018

Study Completion Date

July 31, 2018

Conditions
Pregnancy
Interventions
BEHAVIORAL

PROSPERO

"The intervention is carried out in 3 steps:~1. At the start of the pregnancy: a number of process steps are defined for a patient's pathway adapted to medical, obstetric and social risk factors.~2. During pregnancy: city based doctors and midwives work together with their hospital peers enabling patients to participate through the reporting via a medical information system~3. The entrance in the delivery room: patients are classified as low or high risk for greater vigilance from midwives."

OTHER

control

At the start of the pregnancy, medical, obstetric and social risk factors are checked in the same way than the PROSPERO group. An adapted patient pathway was defined by a Clinical Research Assistant but unreachable from patients, midwifes and physicians. The electronic patient care reporting information system will be disabled and midwifes cannot create the classification checklist for low or high risk delivery.

Trial Locations (2)

69002

Hospices Civils de Lyon, Lyon

69677

Hôpital Femme Mère Enfant, Bron

All Listed Sponsors
lead

Hospices Civils de Lyon

OTHER

NCT02593292 - Program of Research for the Optimization of a Supervised Patient Pathway for Expectant According to Risk in Obstetrics | Biotech Hunter | Biotech Hunter