Alberta Pregnancy Outcomes and Nutrition

Overview

Acronym
APrON
Website
APrON
Investigators
Dr. Nicole Letourneau
University of Calgary
Dr. Bonnie J. Kaplan
University of Calgary
Dr. Deborah Dewey
University of Calgary
Dr. Catherine Field
University of Alberta
Dr. Gerald Giesbrecht
University of Calgary
Dr. Rhonda Bell
University of Alberta
Dr. François Bernier
University of Calgary
Dr. Nalini Singhal
University of Calgary
Dr. Maeve O'Beirne
University of Calgary
Dr. Donna Manca
University of Alberta
Dr. Brenda Leung
University of Lethbridge
Dr. Linda Casey
University of British Columbia
Dr. Jonathan Martin
University of Alberta
Contacts
Dr. Nicole Letourneau
University of Calgary
Andrea Deane
University of Calgary

General Design

Study design
Cohort
Start - End Year
2009 -
General Information on Follow Up (profile, frequency)
Recruitment Target
  • Families
Number of Participants
5,841
Number of Participants with Biological Samples
5,175
Supplementary information about number of participants

Access

Availability of data and biosamples

Possible Access to Data
Possible Access to Biosamples
Other

Sector of research

Possible Access to Data Possible Access to Biosamples
Investigators from the public sector
Investigators from the private sector
Investigators from not-for-profit organization

Transfer

Possible Access to Data Possible Access to Biosamples
Can leave the study facility
Can leave the country

Cost

Possible Access to Data Variable Cost
Possible Access to Biosamples Variable Cost

Cost reduction for co-analyses

Possible Access to Data
Possible Access to Biosamples

Marker Paper

Kaplan BJ, Giesbrecht GF, Leung BM, Field CJ, Dewey D, Bell RC, Manca DP, O'Beirne M, Johnston DW, Pop VJ, Singhal N, Gagnon L, Bernier FP, Eliasziw M, McCargar LJ, Kooistra L, Farmer A, Cantell M, Goonewardene L, Casey LM, Letourneau N, Martin JW; APrON Study Team. The Alberta Pregnancy Outcomes and Nutrition (APrON) cohort study: rationale and methods. Maternal and Child Nutrition. 2014 Jan;10(1):44-60.

PUBMED 22805165

Timeline

Populations

APrON - Mothers

Selection Criteria

Gender
Women only
Minimum age
16
Pregnant Women
  • First trimester
  • Second trimester
Countries
  • Canada
Canadian Provinces
  • Alberta
Territory
Metropolitan areas of Calgary and Edmonton in Alberta
Other Criteria

Sources of Recruitment

General Population
  • Volunteer enrolment
Specific Population
  • Clinic patients
Supplementary Information

Sample Size

Number of Participants
2,189
Number of Participants with Biological Samples
2,041

Data Collection Events

# Name Data sources Data sources - Biosamples Start End
0 APrON - Mothers - First trimester
  • Questionnaires
  • Physical measures
  • Biosamples
  • Blood
2009 (January) 2012 (June)
1 APrON - Mothers - Second trimester
  • Questionnaires
  • Physical measures
  • Biosamples
  • Blood
  • Urine
2009 (May) 2012 (September)
2 APrON - Mothers - Third trimester
  • Questionnaires
  • Physical measures
  • Biosamples
  • Blood
  • Urine
2009 (July) 2012 (November)
3 APrON - Mothers - Birth
  • Other : Medical records
2009 (August) 2013 (February)
4 APrON - Mothers - 12 weeks postpartum
  • Questionnaires
  • Physical measures
  • Biosamples
  • Blood
  • Urine
  • Other : Breast milk
2009 (November) 2013 (May)
5 APrON - Mothers - 24 weeks postpartum
  • Questionnaires
  • Physical measures
2010 (February) 2013 (November)
6 APrON - Mothers - 12 months postpartum
  • Questionnaires
2010 (September) 2014 (June)
7 APrON - Mothers - 24 months postpartum
  • Questionnaires
2011 (August) 2015 (February)
8 APrON - Mothers - 3 years postpartum
  • Questionnaires
2012 (September) 2016 (May)
9 APrON - Mothers - 5 years postpartum
  • Questionnaires
2014 (August) 2018 (May)
APrON - Partners

Selection Criteria

Countries
  • Canada
Canadian Provinces
  • Alberta
Territory
Metropolitan areas of Calgary and Edmonton in Alberta

Sources of Recruitment

Specific Population
  • Other specific population : Partners of the pregnant women already recruited.

Sample Size

Number of Participants
1,483
Number of Participants with Biological Samples
1,343

Data Collection Events

# Name Data sources Data sources - Biosamples Start End
0 APrON - Partners - Second trimester
  • Questionnaires
  • Biosamples
  • Blood
  • Buccal cells
2009 (April) 2012 (December)
1 APrON - Partners - 12 weeks postpartum
  • Questionnaires
2009 (November) 2013 (May)
2 APrON - Partners - 5 years postpartum
  • Questionnaires
2014 (August) 2018 (May)
APrON - Children

Selection Criteria

Newborns
Countries
  • Canada
Canadian Provinces
  • Alberta
Territory
Metropolitan areas of Calgary and Edmonton in Alberta

Sources of Recruitment

Specific Population
  • Other specific population : Newborn children of the women enrolled in the study.

Sample Size

Number of Participants
2,169
Number of Participants with Biological Samples
1,791

Data Collection Events

# Name Data sources Data sources - Biosamples Start End
0 APrON - Children - Birth
  • Other : Medical records
2009 (August) 2013 (May)
1 APrON - Children - 12 weeks postpartum
  • Questionnaires
  • Physical measures
  • Biosamples
  • Blood
  • Buccal cells
2009 (November) 2013 (May)
2 APrON - Children - 24 weeks postpartum
  • Questionnaires
2010 (February) 2013 (August)
3 APrON - Children - 12 months postpartum
  • Questionnaires
2010 (September) 2014 (February)
4 APrON - Children - 24 months postpartum
  • Questionnaires
2011 (August) 2015 (February)
5 APrON - Children - 3 years postpartum
  • Questionnaires
2012 (September) 2016 (May)
6 APrON - Children - 5 years postpartum
  • Questionnaires
2014 (August) 2018 (May)

Participating Studies

Acronym Name Study design Countries

Harmonization Initiatives Included

Acronym Name

Datasets

Name Data Collection Events Variables

Areas of Information Collected

Socio-demographic and economic characteristics
Death
Lifestyle and behaviours
Physical measures and assessments
Birth, pregnancy and reproductive health history
Laboratory measures
Perception of health, quality of life, development and functional limitations
Cognition, personality and psychological measures and assessments
Diseases
Life events, life plans, beliefs and values
Symptoms and signs
Preschool, school and work life
Medication and supplements
Social environment and relationships
Non-pharmacological interventions
Physical environment
Health and community care services utilization
Administrative information

Variables Content Summary

Areas of Information Collected
No Areas of Information Collected
No Scales Collected
Areas of Information Collected per per Population and Data Collection Event
No Areas of Information Collected
No Scales Collected

Networks

Acronym Name Harmonization Initiatives Individual Studies
Last Update: 2021-04-29T17:39:30.305