Trials Sponsors Conditions Drugs Pricing

Conditions

Pregnant Women and Partners

Outcome Measures

Primary Outcomes (1)

Change from Baseline Perinatal Knowledge
Measured with an adapted version of the Health Pregnancies Knowledge Survey
10-20 weeks of pregnancy; 33 weeks of pregnancy

Secondary Outcomes (10)

Change from Baseline Psychological Distress
10-20 weeks of pregnancy; 33 weeks of pregnancy; 6 weeks after child birth
Change from Baseline Breastfeeding Self-Efficacy
10-20 weeks of pregnancy; 33 weeks of pregnancy; 6 weeks after child birth
Change from Baseline Anxiety
10-20 weeks of pregnancy; 33 weeks of pregnancy; 6 weeks after child birth
Change from Baseline Self-Efficacy in the Parenting Role
10-20 weeks of pregnancy; 33 weeks of pregnancy; 6 weeks after child birth
Change from Baseline Depression
10-20 weeks of pregnancy; 33 weeks of pregnancy; 6 weeks after child birth
+5 more secondary outcomes

Study Arms (3)

Group prenatal education

Prenatal education delivered in-person by health and social services centers

Other: Prenatal education

Online prenatal education

Online prenatal education provided or recommended by health and social services centers

Other: Prenatal education

Control group

Absence of prenatal education

Interventions

Prenatal educationOther

Observational study : natural distribution of participants between groups

Group prenatal educationOnline prenatal education

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersYes

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

Pregnant women and partners. Recruitment methods : * By the research team in hospital waiting rooms, before ultrasound appointments * By health professionals in community centers during routine appointments * Posters with the team's contact information * Registration using advertisements on Facebook

You may qualify if:

weeks of pregnancy

Sponsors & Collaborators

Fonds de la Recherche en Santé du Québec
Governmentcollaborator
CHU de Quebec-Universite Laval
Otherlead

Study Sites (1)

CHU de Québec

Québec, G1L3L5, Canada

MeSH Terms

Interventions

Prenatal Education

Intervention Hierarchy (Ancestors)

Patient Education as TopicHealth EducationPreventive Health ServicesHealth ServicesHealth Care Facilities Workforce and Services

Enrollment

1,208 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

February 16, 2018

First Posted

March 14, 2018

Study Start

June 18, 2018

Actual (reported)

Impacts of Online and Group Perinatal Education

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (10)

Study Arms (3)

Group prenatal education

Online prenatal education

Control group

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Interventions

Intervention Hierarchy (Ancestors)

Enrollment

Study Design

Study Record Dates

Data Sharing

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (10)

Study Arms (3)

Group prenatal education

Online prenatal education

Control group

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Interventions

Intervention Hierarchy (Ancestors)

Enrollment

Study Design

Study Record Dates

Data Sharing

Source record

Locations