Information During Maternity

Pregnancy Related Clinical Trial

Official title:

Information During Maternity

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03305601
• Other study ID #: SMARTMATER
• Status: Completed
• Phase: N/A
• First received: October 4, 2017
• Last updated: October 9, 2017
• Start date: July 8, 2016
• Est. completion date: July 31, 2017

Study information

• Verified date: October 2017
• Source: Groupe Hospitalier Paris Saint Joseph
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

During the pregnancy , it's now compulsary for the doctors to inform pregnant women and the couple about the medical, non medical informations and explain the physiological changes . As usual, medical staff and doctors explain and inform by oral and with a booklet patient.

In order to cluster and make more accessible these informations, the maternity team of GHPSJ has developed an application on smartphone . If this application has been evaluated on his contents and accordance to recommendations, there is no evaluation about the satisfaction of patient.

The aim is to study the impact of this kind of application on pregnant women satisfaction.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 104
• Est. completion date: July 31, 2017
• Est. primary completion date: January 31, 2017
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• single pregnancy

• delivery at 37 weeks of amenhorrhea

• age > 18

• with an email address

Exclusion Criteria:

• refusing participation

• foetal pathology

Related Conditions & MeSH terms

• Pregnancy Related

Intervention

Other:
• application on smarthphone
application on smarthphone

Locations

Country	Name	City	State
France	Groupe Hospitalier Paris Saint Joseph	Paris	Ile-de-France

Sponsors (1)

Lead Sponsor	Collaborator
Groupe Hospitalier Paris Saint Joseph

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	satisfaction score		9 months