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Evaluation of a Peer Counseling Breastfeeding Support Program for Mother-preterm Infant Dyads

Breastfeeding Peer Counselling for Mothers of Preterm Neonates: a Stepped- Wedge Cluster Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03156946
Acronym
ALAIS
Enrollment
1774
Registered
2017-05-17
Start date
2018-11-05
Completion date
2022-12-22
Last updated
2025-11-21

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

Conditions

Infant Premature

Keywords

breastfeeding, mother-to-mother support, lactation consultant, stepped wedge cluster randomized trial, peer counseling

Brief summary

Breastfeeding has a fundamental impact on the short-, medium- and long-term health of children and has an important impact on women's health. Breastfeeding protects against gastrointestinal and respiratory illnesses and is associated with better cognitive development in childhood, particularly in preterm infants. Despite these potential benefits, preterm infants experience lower rates of breastfeeding initiation and continuation compared to term infants. The use of breastfeeding peer support initiatives, in which advice is given by experienced and trained peer counselors, is an effective way to promote and support breastfeeding, regardless of a woman's socioeconomic status. Several small studies have shown that breastfeeding peer support initiatives were effective for preterm infants and that this efficacy was increased by the co-intervention of lactation consultants. The purpose of this study is to develop and to evaluate the effectiveness of a breastfeeding support program among mother-preterm infant dyads in Europe, by evaluating the impact of the intervention on 1) breastfeeding rates, 2) morbidity and mortality during the hospitalization, 3) children's cognitive development and behavior 4) mothers' mental health, 4) costs benefits. The breastfeeding support program will include peer counselors under the supervision of lactation consultants. Breastfeeding counselors will be voluntary mothers who have had a positive breastfeeding experience with at least one preterm infant. After a training course, they will meet the future or new mothers by face-to-face and share their experiences at least once a week during hospitalization and provide phone support up to 1 month after discharge from hospital. The study design will be a stepped wedge cluster trial conducted in 8 NICU in Europe (France, Switzerland and Belgium). Infants and mothers will be followed up from the time of hospitalization in the maternity and NICU up to 6 months after the discharge. The cost analysis will be performed in a subgroup of mother-preterm infant dyads that will be followed up at 24-months after their discharge

Interventions

BEHAVIORALbreastfeeding mother-to-mother support

The mother-infant dyads in the intervention arm will receive breastfeeding mother-to-mother support from the hospitalization in the maternity and NICU up to 1 month after discharge. The intervention will be in addition to the usual or routine care. Breastfeeding counselors will be voluntary mothers who breastfed their own preterm infant (aged between 6 months and 5 years at the time of the study) for a minimum of 2 months, and who have had a positive personal breastfeeding experience, and who have undertaken a training course.

BEHAVIORALControl

The mother-infant dyads in the control arm will continue to receive the usual/routine care provided by participating centers during the hospitalization and Mother and Infant Protection service after discharge.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

stepped wedge

Eligibility

Sex/Gender
ALL
Age
No minimum to 35 Weeks
Healthy volunteers
No

Inclusion criteria

* any infant born \<35 weeks' gestation, * hospitalised in NICU before 24 hours old * and younger than 168 hours (7 days) old.

Exclusion criteria

* infant with foetal malformation that is life-threatening * infant with medical contraindication for breastfeeding * parent(s)' non-consent to be involved in the study * mother with prolonged medical contraindication for breastfeeding * mother with psychiatric disorders making breastfeeding support impossible * if no communication is possible with the mother * if the level of communication with the mother does not allow breastfeeding support, with or without a third party

Design outcomes

Primary

MeasureTime frameDescription
Breastfeeding continuation ratesat corrected postnatal age of 2 monthsBreastfeeding will be defined as the consumption of any mother's own milk. It will be classed as exclusive when all of the fed milk is the mother's own milk, or mixed when it will be completed by other milk and/or food.

Secondary

MeasureTime frameDescription
Breastfeeding rateat 2 months of corrected age
Breastfeeding durationat 6 months of corrected age
Costs effectiveness of breastfeedingup to first two years of lifeCosts will include initial hospitalization, hospital readmissions, outpatient visits and tests.
Neonatal severe complicationsat 36 weeks of corrected ageMorbidity outcomes will include intraventricular haemorrhage grade≥3, periventricular leucomalacia, sepsis (proven or clinical), persistent ductus arteriosus requiring treatment, necrotising enterocolitis grade≥2, and bronchopulmonary dysplasia (need of oxygen and/or ventilation support at 36 weeks of corrected age), retinopathy of prematurity grade\>2.
Death ratesat 36 weeks of corrected ageMorbidity outcomes will include intraventricular haemorrhage grade≥3, periventricular leucomalacia, sepsis (proven or clinical), persistent ductus arteriosus requiring treatment, necrotising enterocolitis grade≥2, and bronchopulmonary dysplasia (need of oxygen and/or ventilation support at 36 weeks of corrected age), retinopathy of prematurity grade\>2.
Infant behavioursat corrected postnatal age of 6 monthsBehavior will be assessed by the validated Infant Behavior questionnaire completed by mothers.
cost consequence of breastfeedingup to first two years of lifeCosts will include hospitalization rate and mortality between the two strategies.
Mother-Infant bondingat corrected postnatal age of 6 monthsDisabilities will include cerebral palsy, mental retardation assessed by the developmental quotient less than 85 on the Brunet- Lézine scale, and visual and hearing deficits. -Infant bonding assessed by the Mother-Infant Bonding Scale (MIBS)
Rate of breastfeeding initiatedat 2 months of corrected age
Neurodevelopment rate by Brunet Lézine scaleat corrected postnatal age of 24 months
Anxiety by the Hospital Anxiety and Depression Scale (HADS)at corrected postnatal age of 6 months
Depression by the Edinburgh Postnatal Depression Scale.at corrected postnatal age of 6 months
Posttraumatic stress by the Post-traumatic stress disorder Checklist version DSM-5 (PCL-5)at corrected postnatal age of 6 months
Parents stress by the Parenting Stress Index Fourth Edition Short Form (PSI-4 SFat corrected postnatal age of 6 months
Feasibility of the breastfeeding support program24 monthsTo assess the feasibility of the intervention, we will depict : - the socio-demographic characteristics of breastfeeding counselors - and the number of contacts between mothers and breastfeeding counselors (frequency and duration) and the information
Acceptability of the breastfeeding support program24 monthsTo assess the acceptability of the breastfeeding support program, we will collect : * the perception of breastfeeding support by mothers and their spouses, by staff members (lactation consultant, nurses) in each participating centers and by breastfeeding counselors. * the number of mothers who refuse to be managed by a breastfeeding counselors and their reasons, * the duration of each breastfeeding counselor intervention and the number of mothers who will stop the intervention before 1 month after the hospital discharge.
Disability rateat corrected postnatal age of 24 monthsDisabilities will include cerebral palsy, mental retardation assessed by the developmental quotient less than 85 on the Brunet- Lézine scale, and visual and hearing deficits.

Countries

Belgium, France, Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026