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Continuous Delivery Room Skin-to-skin-study for Moderate and Late Preterm Infants

Continuous Delivery Room Skin-to-skin-study for Moderate and Late Preterm Infants

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05975203
Acronym
COSY
Enrollment
60
Registered
2023-08-03
Start date
2023-08-04
Completion date
2028-12-31
Last updated
2026-02-20

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

Conditions

Preterm Birth, Mother-Infant Interaction, Infant Development

Keywords

preterm behavioral epigenetics, skin-to-skin contact

Brief summary

The goal of this randomized controlled trial is to compare the effect of direct skin-to-skin contact in moderate and late preterm infants. The main questions it aims to answer are: * does skin-to-skin contact in moderate and late preterm infants influence gene expression in the stress signaling pathway? * does skin-to-skin contact in moderate and late preterm infants improve the short- and long-term outcome? Participants will either get immediate separation after vaginal birth or receive immediate skin-to-skin contact. Researchers will compare these two groups to answer the proposed questions.

Detailed description

The planned study investigates prospectively the effect of early intervention (skin-to-skin contact in the delivery room) in moderate and late preterm infants on neonatal programming by determining gene expression in the stress signaling pathway. The working hypothesis of our project is that the intervention will affect gene expression in a way that subsequently leads to better long-term psycho-social and neurological development of these preterm infants. The study aims to improve the understanding of the correlation of behavioral and epigenetic parameters and prove the underlying hypothesis of a novel mechanistic link between immediate skin-to-skin contact in the delivery room and life-long stress tolerance.

Interventions

Immediately after delivery the infant will receive skin-to-skin contact with the mother.

Sponsors

University of Cologne
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Due to the nature of the intervention blinding of participant and care provider is not possible. The investigators are part of the care providing team.

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* preterm birth between gestational age of 32 0/7 and 36 6/7 weeks * vaginal delivery * singleton * informed consent before birth

Exclusion criteria

* malformations or syndromes of the infant * resuscitation of the infant * maternal psychological or severe physical illness * lack of German language skills

Design outcomes

Primary

MeasureTime frameDescription
gene expression in candidate genes of the stress signalling pathway36 to 72 hours after birthDNA will be extracted from peripheral white blood cells and mucosal epithelial cells. The expression of candidate genes of the stress signaling pathways are investigated. The candidate genes are glucocorticoid receptor (NR3C1), corticotropin releasing hormone (CRH), corticotropin-releasing hormone receptor 1 and 2 (CRHR1/2), serotonin transporter (slc6a4), vasopressin and brain-derived neurotrophic factor.

Secondary

MeasureTime frameDescription
mother-child-interactioncorrected 6 months of ageMother-child-interaction is investigated using Mannheim Rating Scales. Therefore a five-minute-videotape of the mother changing the infant's diapers and playing with the infant is used. Mannheim Rating Scales is a good validated standardized observation instrument. Stimulation and response from the mother as well from the infant are being recorded. Different communication channels can be used by mother and child (vocal, facial or motor). All behaviors are analysed at intervals of five seconds (event coding). Then the values are formed from the sum of the coded events. The scale ranges from 0 to 60. If there is no interaction, the scale is 0. If there is an interaction in each interval (every 5 seconds in a 5 minute videotape), the scale is 60. The mother-child interaction is better if the scale is higher.
General Movementscorrected 3 months of ageThe early infant development will be analyzed by general movements assessment by Prechtl. It is a validated diagnostic tool for the functional assessment of the young nervous system.
maternal depressionat inpatient discharge (assessed from 3 to 60 days of life), corrected 6 and 24 months of ageMaternal depression is assessed with the German long form of the Center for Epidemiological Studies Depression Scale (CES-D). It is a self-report questionnaire to measure depressive symptoms and it consists of 20 questions. For each question the response choice are assigned point values (how often a symptom occurred during the last week). The point values are summed to a total measure score. The score ranges from 0 to 60. Zero points represents no symptoms of depression, a score of 15 or higher is interpreted to indicate a risk of depression.
social supportat inpatient discharge (assessed from 3 to 60 days of life), corrected 24 months of ageSocial support is assessed with the short version of the German questionnaire for social support (Fragebogen zur sozialen Unterstützung, questionnaire on social support) scale (F-SozU K-22). The questionnaire records the subjectively perceived or anticipated support from the social environment. There are 22 items and the test person can indicate the degree of agreement on a five-level Likert scale (from 1 = does not apply to 5 = applies completely). The scale ranges from a minimum of 22 points to a maximum of 110 points. The higher the score, the better the subjectively perceived or anticipated support.
socio-economic statusat inpatient discharge (assessed from 3 to 60 days of life)There will be a question to the household income per month and the parents' highest school-leaving certificate as well as the housing situation.
breastfeedingat inpatient discharge (assessed from 3 to 60 days of life) and corrected six months of ageThere will be a question about breastfeeding.
impact of event scalecorrected 6 months of ageSymptoms for post-traumatic stress is assessed with the impact of event scale - revised (IES-R). It is a self-report questionnaire and consists of 22 questions. For each question the response choice are assigned point values (how often a symptom occurred during the last week). The sub-scale values are summed by the corresponding sub-scale items. The three sub-scales are: intrusion, avoidance and hyperarousal. The overall result is calculated by a formula. The score ranges from -4,36 to 2,99. A result above 0 is interpreted to indicate a risk of post-traumatic stress disorder.
Parental Bondingcorrected 6 and 24 months of ageParental Bonding is assessed with the parental bonding questionnaire (PBQ). It consists of 25 items and each item is rated on a scale from 0 to 3 points (response range from "very like" to "very unlike"). There are four sub-scales and the point values of each sub-scale are summed to a total measure score. The four sub-scales are: impaired bonding, rejection and anger, anxiety about care, risk of abuse. The higher the score, the higher the risk of a disorder in each area of the sub-scale.
Parental Stresscorrected 6 and 24 months of ageParental stress is assessed with the German form of the parenting stress index (PSI). It consists of 48 items. The test person can indicate the degree of agreement on a five-level Likert scale (from 1 = does not apply to 5 = applies completely). There are 12 subscales, each consisting of 4 items and the points on the Likert scale are added. In each subscale there can be a minimum of 4 and a maximum of 20 points. The higher the score, the higher the parental stress.
reactivity of hypothalamic-pituitary-adrenal-axis36 to 72 hours after birth and corrected 24 months of ageSalivary cortisol is measured before and 20 minutes after heel lance, respectively after a stressful testing. The saliva is collected by a small cotton roll, which is placed in the infants' mouth. The cortisol is assayed in duplicate using an immunoassay, which is a validated test.

Countries

Germany

Contacts

CONTACTKatrin Mehler, PD Dr.
katrin.mehler@uk-koeln.de004922147885663
CONTACTAngela Kribs, PD Dr.
angela.kribs@uk-koeln.de004922147885663
PRINCIPAL_INVESTIGATORKatrin Mehler, PD Dr.

University of Cologne

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026