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Providing Postnatal Breastfeeding Support Through the Canada Prenatal Nutrition Program

Effectiveness and Feasibility of Providing Postnatal Breastfeeding Support to Vulnerable Mothers as an Extension to the Canada Prenatal Nutrition Program

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03589963
Acronym
PINSTEP-4
Enrollment
151
Registered
2018-07-18
Start date
2018-11-01
Completion date
2021-07-13
Last updated
2022-05-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breastfeeding, Breastfeeding, Exclusive, Complementary Feeding, Infant Nutrition

Brief summary

The Canada Prenatal Nutrition Program (CPNP) aims to improve birth outcomes among Canadian women in challenging life circumstances, including those who are adolescents, newcomers, low-income or single mothers. The CPNP strongly promotes breastfeeding prenatally, resulting in high initiation rates, but continued postnatal support is needed to optimize breastfeeding duration and exclusivity. The aim of this research is to investigate the effects of adding postnatal lactation support as an extension to the CPNP on breastfeeding duration and exclusivity in the first six months postpartum. The research will be conducted at two CPNP sites in Toronto, Parkdale Queen West Community Health Centre and The Stop Community Food Centre. A quasi-experimental design will be used to compare the infant feeding practices of CPNP clients before and after introduction of a postnatal lactation support intervention which will include in-home professional lactation support and provision of high-quality breast pumps. These services will be delivered as CPNP program components and will be accessible to all clients at the two participating sites during the post-intervention period. Infant feeding practices will be assessed by a questionnaire administered at 2 weeks, 1, 2, 3, 4, 5 and 6 months postpartum. The hypothesis is that significantly more mothers in the post-intervention group will be exclusively breastfeeding at four months postpartum. The effect is expected to be mediated through increased breastfeeding self-efficacy, which will be assessed using validated scales prenatally and at 2 weeks and 2 months postpartum.

Interventions

BEHAVIORALPostnatal Lactation Support

In-home breastfeeding support delivered by professional lactation consultants and provision of a high-quality breast pump

Sponsors

Sprott Foundation
CollaboratorUNKNOWN
Parkdale Queen West Community Health Centre
CollaboratorUNKNOWN
University of Toronto
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
15 Years to 49 Years
Healthy volunteers
Yes

Inclusion criteria

* CPNP clients registered prenatally * intention to initiate breastfeeding * intention to remain in Toronto with the infant for 6 months postpartum * willing to share contact information * birth at 34 weeks gestation or later

Exclusion criteria

* preterm birth (below 34 weeks) * infant has congenital abnormality or medical condition affecting feeding * mother or infant still in hospital at 2 weeks postpartum

Design outcomes

Primary

MeasureTime frameDescription
Exclusive breastfeeding at 4 months postpartumbirth to 4 months postpartumReported exclusive breastfeeding at four months postpartum assessed by a prospective infant feeding questionnaire

Secondary

MeasureTime frameDescription
Duration of any breastfeeding in the first six months postpartumbirth to 6 months postpartumDuration of any breastfeeding from birth to 6 months assessed by a prospective infant feeding questionnaire
Duration of exclusive breastfeeding in the first six months postpartumbirth to 6 months postpartumDuration of exclusive breastfeeding from birth to 6 months assessed by a prospective infant feeding questionnaire
Age of introduction of breastmilk substitutesbirth to 6 months postpartumReported timing of the introduction of breastmilk substitutes from birth to 6 months in response to a prospective infant feeding questionnaire
Age of introduction of complementary foodsbirth to 6 months postpartumReported timing of the introduction of complementary foods from birth to 6 months in response to a prospective infant feeding questionnaire

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026