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NCT Number: NCT07533578

Chrononutrition in Preterm Infants: a Randomised Controlled Trial of Time-matched Breast Milk Feeding and Its Effects on Sleep and Circadian Development

This study investigates whether the timing of feeding expressed breast milk influences infant sleep and circadian (day-night) development in preterm infants.

In early life, infants produce very little of the hormone melatonin, which plays a key role in regulating sleep and circadian rhythms. Breast milk naturally contains melatonin, and its levels vary across the day, with higher concentrations at night. This variation may provide important biological signals that help infants develop healthy sleep-wake patterns.

However, expressed breast milk is often fed without considering the time it was expressed. This may disrupt the transfer of circadian signals from mother to infant.

The aim of this randomised controlled trial is to determine whether feeding expressed breast milk according to the time of expression (e.g. giving night-time milk at night) improves sleep consolidation and circadian development compared with usual feeding practices.

A total of 200 preterm infants born between 32+0 and 36+6 weeks' gestation who are receiving expressed breast milk will be enrolled and randomly assigned to one of two groups:

Intervention group: preterm infants receive expressed breast milk matched to the time of day it was expressed (day, evening or night)

Control group: preterm infants receive expressed breast milk without regard to timing (usual practice)

The main outcome is sleep consolidation at 6 months of age, measured objectively using actigraphy (a small wearable device that records sleep and activity). Additional outcomes include sleep patterns over time, circadian development, melatonin exposure, gut microbiota composition, and clinical outcomes such as infections and neurodevelopment.

The intervention does not involve any medication and uses the infant's usual nutrition. Risks are minimal and mainly relate to the additional effort required for milk labelling and timing.

This study will provide evidence on whether a simple, low-risk change in feeding practice can support infant sleep and early-life circadian development, with potential benefits for child health and family well-being.

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Key information

Age range

0 day–1 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kantonsspital Luzern, Universität Luzern

Lucerne, Switzerland

About this study

This study investigates whether the timing of feeding expressed breast milk influences infant sleep and circadian (day-night) development in preterm infants.

In early life, infants produce very little of the hormone melatonin, which plays a key role in regulating sleep and circadian rhythms. Breast milk naturally contains melatonin, and its levels vary across the day, with higher concentrations at night. This variation may provide important biological signals that help infants develop healthy sleep-wake patterns.

However, expressed breast milk is often fed without considering the time it was expressed. This may disrupt the transfer of circadian signals from mother to infant.

The aim of this randomised controlled trial is to determine whether feeding expressed breast milk according to the time of expression (e.g. giving night-time milk at night) improves sleep consolidation and circadian development compared with usual feeding practices.

A total of 200 preterm infants born between 32+0 and 36+6 weeks' gestation who are receiving expressed breast milk will be enrolled and randomly assigned to one of two groups:

Intervention group: preterm infants receive expressed breast milk matched to the time of day it was expressed (day, evening or night) Control group: preterm infants receive expressed breast milk without regard to timing (usual practice)

The main outcome is sleep consolidation at 6 months of age, measured objectively using actigraphy (a small wearable device that records sleep and activity). Additional outcomes include sleep patterns over time, circadian development, melatonin exposure, gut microbiota composition, and clinical outcomes such as infections and neurodevelopment.

The intervention does not involve any medication and uses the infant's usual nutrition. Risks are minimal and mainly relate to the additional effort required for milk labelling and timing.

This study will provide evidence on whether a simple, low-risk change in feeding practice can support infant sleep and early-life circadian development, with potential benefits for child health and family well-being.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Preterm infants born between 32+0 and 36+6 weeks' gestation
  • Age ≤ 1 month at enrolment
  • Infants routinely receiving expressed breast milk (fully or partially breastfed)
  • Written informed consent obtained from parent(s) or legal representative(s)
  • Ability of caregivers to comply with study procedures including milk labelling and feeding according to study allocation

Exclusion criteria

  • Prenatal exposure to illicit drugs (e.g. cannabis, cocaine, heroin, opiates) or significant alcohol exposure
  • Major congenital malformations or congenital infections
  • Significant underlying disease (excluding transient neonatal conditions such as feeding difficulties, hyperbilirubinaemia, hypoglycaemia, anaemia, respiratory distress syndrome, or apnoea-bradycardia syndrome)

Treatment and study plan

Chronobiologically Timed Feeding of Expressed Breast Milk

Other

Expressed breast milk is labelled at the time of expression and categorised into predefined time windows:

Day milk: 06:00-17:59 Evening milk: 18:00-21:59 Night milk: 22:00-05:59 Infants are fed milk corresponding to the appropriate time-of-day window to align feeding with circadian rhythms. Caregivers receive standardised training, and adherence is monitored using feeding logs.

Usual Feeding Practice (Untimed Expressed Breast Milk)

Other

Expressed breast milk is fed without consideration of the time of expression. Milk handling, storage, and preparation follow standard procedures. No modification of milk composition or additional substances are introduced.

Primary outcomes

  1. Sleep consolidation (longest nocturnal sleep bout)

    Time frame: At 6 months of age

    Measured by actigraphy

Secondary outcomes

  1. Sleep fragmentation

    Time frame: At 2, 4, 6, 12, and 24 months

    Assessed by actigraphy and sleep-wake diaries

  2. Circadian rhythm development (day-night activity ratios and circadian function index)

    Time frame: At 2, 4, 6, 12, and 24 months

    Assessed by actigraphy

  3. Parent-reported sleep outcomes

    Time frame: At 2, 4, 6, 12, and 24 months

    Assessed using the Brief Infant Sleep Questionnaire (BISQ)

  4. Melatonin circadian profiles

    Time frame: At 2, 4, 6, 12, and 24 months

    In breast milk and infant stool

  5. Intestinal microbiota composition

    Time frame: At 2, 4, 6, 12, and 24 months

    Assessed by shotgun metagenomic sequencing

  6. Infection rates

    Time frame: At 2, 4, 6, 12, and 24 months

    Clinically diagnosed infections (including otitis media and lower respiratory tract infections), assessed via medical records and parental report

  7. Neurodevelopmental outcomes

    Time frame: 24 months

    Bayley Scales of Infant and Toddler Development (Bayley-III)

Study contacts

Contact information is provided by the study sponsor or research team.

Petra Zimmermann, MD, PhD

CONTACT

[email protected]

+4141 205 82 69

Sponsors and collaborators

Lead sponsor

Luzerner Kantonsspital

Other

Registry information

Important dates

Study start
2026
Primary completion
2030
Study completion
2031
First posted
Apr 16, 2026
Registry last updated
Apr 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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