Evidence map›Paper›PMID 36703104›Full record

ArticleBMC pregnancy and childbirth2023

Study protocol for the sheMATTERS study (iMproving cArdiovascular healTh in new moThERS): a randomized behavioral trial assessing the effect of a self-efficacy enhancing breastfeeding intervention on postpartum blood pressure and breastfeeding continuation in women with hypertensive disorders of pregnancy.

Natalie Dayan, Graeme Smith, Atanas Nedelchev, Haim Abenhaim, Richard Brown, Deborah Da Costa, Suhad Ali, Jesseca Perlman, Tuong-Vi Nguyen, Cindy-Lee Dennis and 2 more

Registry-linked trialOpen access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMC pregnancy and childbirth, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04580927 (Improving Cardiovascular Health in New Mothers), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04580927 naunknown statusnot on this map

Improving Cardiovascular Health in New Mothers: Multi-Centre Open-Label Randomized Trial of a Breastfeeding Intervention to Improve Breastfeeding Practices and Lower Blood Pressure in Women With Hypertensive Disorders of Pregnancy

TypeinterventionalSponsorMcGill University Health Centre/Research Institute of the McGill University Health CentreRan2021 to 2025Enrolled221ConditionsHypertensive Disorder of Pregnancy, Pregnancy Complications, Pre-Eclampsia, Hypertension, Pregnancy-InducedArmsBreastfeeding self-efficacy (BSE)
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
  2. Implementation strategies: bridging obstetrics and long-term care.American journal of obstetrics & gynecology MFM · 2026
    Review
  3. Breastfeeding and Maternal and Child Cardiometabolic Outcomes 10-14 Years after Delivery.Breastfeeding medicine : the official journal of the Academy of Breastfeeding Medicine · 2025
    Article
  4. Tracking of blood pressure levels from childhood.Pediatric nephrology (Berlin, Germany) · 2025
    Review
  5. Article
  6. Article
  7. High-risk pregnancy and risk of breastfeeding failure.The Journal of the Egyptian Public Health Association · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 1 country.

Natalie DayanDepartment of Medicine, McGill University, Montréal, Canada. natalie.dayan@mcgill.ca.ORCID http://orcid.org/0000-0002-7747-2343
Graeme SmithDepartment of Obstetrics and Gynecology, Queen's University, Kingston Health Science Centre, Kingston, Canada.
Atanas NedelchevDepartment of Obstetrics and Gynecology, St. Mary's Hospital Center, Montreal, Canada.
Haim AbenhaimDepartment of Obstetrics and Gynecology, McGill University, Montréal, Canada.
Richard BrownDepartment of Medicine, McGill University, Montréal, Canada.
Deborah Da CostaDepartment of Medicine, McGill University, Montréal, Canada.
Suhad AliDepartment of Medicine, McGill University, Montréal, Canada.
Jesseca PerlmanCentre for Outcomes Research and Evaluation (CORE), Research Institute of the McGill University Health Centre (RI-MUHC), 5252 de Maisonneuve West, 2B.40, Montreal, Quebec, H4A 3S5, Canada.
Tuong-Vi NguyenDepartment of Obstetrics and Gynecology, McGill University, Montréal, Canada.
Cindy-Lee DennisLaurence S Bloomfield Faculty of Nursing, University of Toronto, Toronto, Canada.
Wael AbdelmageedDepartment of Medicine, McGill University, Montréal, Canada.
Sonia SemenicCentre for Outcomes Research and Evaluation (CORE), Research Institute of the McGill University Health Centre (RI-MUHC), 5252 de Maisonneuve West, 2B.40, Montreal, Quebec, H4A 3S5, Canada.
McGill University Health Centre · CAMcGill University · CAJewish General Hospital · CAQueen's University · CASt Mary's Hospital Centre · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIndividuals with hypertensive disorders of pregnancy (HDP) have an elevated lifetime risk of chronic hypertension, metabolic syndrome, and premature cardiovascular disease. Because breastfeeding duration and exclusivity have been associated in observational studies with improved cardiovascular health, optimizing breastfeeding in those with HDP might be an unrealized cardio-prevention approach, in particular because individuals with HDP have more breastfeeding challenges. Breastfeeding supportive interventions targeting one's breastfeeding self-efficacy have been shown to improve breastfeeding rates.

methodsWe designed an open-label, multi-center 1:1 randomized behavioral trial to test whether a previously validated self-efficacy enhancing breastfeeding intervention can improve breastfeeding duration and/or exclusivity, and lower postpartum blood pressure at 12 months. Randomization is computer-generated and stratified by site (four hospitals in Montreal, Quebec and one hospital in Kingston, Ontario; all in Canada). Included are breastfeeding participants with HDP (chronic/gestational hypertension or preeclampsia) who delivered a live singleton infant at > 34 weeks, speak English or French, and have no contraindications to breastfeeding. Informed and written consent is obtained at hospitalization for delivery or a re-admission with hypertension within 1 week of discharge. Participants assigned to the intervention group receive a breastfeeding self-efficacy-based intervention delivered by a trained lactation consultant in hospital, with continued reactive/proactive support by phone or text message for up to 6 months postpartum. Regardless of group assignment, participants are followed for self-reported outcomes, automated office blood pressure, and home blood pressure at several time points with end of follow-up at 12 months. DISCUSSION: This study will assess whether an intensive nurse-led behavioral intervention can improve breastfeeding rates and, in turn, postpartum blood pressure - an early marker for atherosclerotic cardiovascular disease. If effective, this form of enhanced breastfeeding support, along with closer BP and metabolic surveillance, can be implemented broadly in individuals lactating after HDP.

trial registrationClinicalTrials.gov, # NCT04580927 , registered on Oct 9, 2020.

Indexed as

Cardiovascular DiseasesHypertension, Pregnancy-InducedPre-EclampsiaBlood PressureBreast FeedingFemaleHumansInfantLactationMulticenter Studies as TopicOntarioPostpartum PeriodPregnancyRandomized Controlled Trials as TopicSelf EfficacyBreastfeedingHypertensive disorders of pregnancyMaternal healthPostpartum cardiovascular healthSelf-efficacy

Identifiers

PMID36703104
PMCPMC9878496
OpenAlexW4318067256

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.