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NWO-FCB project: stress and human breastmilk composition

NWO-FCB project: stress and human breastmilk composition - Amsterdam Mothersmilk Study (AMS)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON45377
Enrollment
180
Registered
2017-05-02
Start date
2017-11-09
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

borstvoeding, stress stress

Interventions

None listed

Sponsors

Universiteit van Amsterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - written informed consent - maternal age > 18 years - Mother is planning to fully breastfeed their infant during the first month after giving birth

Exclusion criteria

Exclusion criteria: - Maternal use of systemic glucocorticoid-medication after giving birth - Maternal hepatic or renal disorder - Maternal use of SSRI - Maternal pre-existing or gestational diabetes - Major congenital anomalies of the neonate

Design outcomes

Primary

MeasureTime frame
- Biological measures of maternal stress: cortisol/cortisone levels in maternal saliva - Psychological measures of maternal stress: perceived stress - Breast milk composition (micronutrient content, macronutrient content, fatty acid profile, metabolite content, cortisol/cortisone content)

Secondary

MeasureTime frame
- (Childhood) stress history of the mother - Perceived maternal stress during pregnancy - Infant temperament assessed at 3 months of age - Anthropometrics of the infant (length, bodyweight, head circumference at 1, 2, 3, months of age, which will be collected during the standard visits at the consulatiebureau) - Cortisol content in the infant faecal samples - Food intake of the mother (during the early-lactation phase)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)