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A Pilot Randomized Controlled Trial of the Effects of Daily Skin-to-skin Contact (PRCTS2S)

A Pilot Randomized Controlled Trial of the Effects of Daily Skin-to-skin Contact Compared to Standard Care on the Stress Responses of Late Preterm Infants in the First Week of Life

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04368767
Acronym
PRCTS2S
Enrollment
8
Registered
2020-04-30
Start date
2020-08-03
Completion date
2020-09-30
Last updated
2020-11-12

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

Conditions

Mother-Infant Interaction, Oxidative Stress, Premature Baby 33 to 36 Weeks

Brief summary

Late preterm infants are at risk of experiencing inadequate glycogen stores with immature glucose metabolism and increased adenosine triphosphate (ATP) degradation, which indicates cellular increased and stress. Processes mediating infant acute/chronic stress symptoms and their biochemical effects have not been adequately investigated. Skin-to-skin contact (SSC), also known as Kangaroo Mother Care (KMC), is as an intervention that activates mechanisms of energy preservation that decrease stress in preterm infants. SSC has been shown in numerous clinical trials to reduce mortality and morbidity by stabilization of breathing, thermal regulation, oxygen saturation, and heart rate. SSC also reduces behavioral distress during painful and stressful procedures and improves breast-feeding parent bonding. However, little is known about how SSC affects biomarkers of stress and energy expenditure in late preterm infants in the first week of life. The aim of this pilot randomized controlled trial is to evaluate changes in biomarkers of stress, stress modulation and energy expenditure in late preterm infants who receive two hours of continuous SSC care or two hours of lying undisturbed in an incubator administered daily for 3 consecutive days in the first week of life, and to provide preliminary data for future research comparing the effects of usual incubator care with prolonged SSC on stress biomarkers in preterm infants.

Interventions

BEHAVIORALSkin-to-skin

Skin-to-skin contact will be performed for two hours daily for three consecutive days in the first week of life, usually in the afternoon. This time interval will allow all pre-intervention sample collection to begin 1 hour after the infant's feeding schedule in the afternoon. After pre-intervention measures of axillary temperature, heart rate, respiratory rate, and oxygen saturation by pulse oximetry (SPO2) are obtained; cotton balls placed in the diaper for urine collection will be removed and stored in an appropriate container. Salivary oxytocin and cortisol will be collected per protocol below. Mothers will be requested to sit in reclining chairs with a front opened blouse or hospital gown. Infants will be removed from the incubator and placed naked except for a diaper and hat directly onto the skin between the mother's breasts and covered with a blanket. All infants will be monitored. After the two hours of SSC is completed, the infant will be returned to the incubator.

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

We will use a randomized controlled trial design to examine feasibility of the prolonged SSC intervention in the first week of life for late preterm infants and to provide preliminary data for future research to compare the effects of usual incubator care with prolonged SSC on biomarkers of stress in late preterm infants in the first week of life.

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Infants between 34 weeks and 0/7 days through 35 weeks and 6/7 days gestational age * Medically stable as determined by a Neonatal Acute Physiology- Perinatal Extension SNAPPE -II (SNAPPE-II) score of less than 9 * Mothers able to read and write English * Mothers have no medical contraindications to holding their infant in SSC for up to 2 hours

Exclusion criteria

* Surgery in the first week of life * Intraventricular hemorrhage (IVH) of grade 3 or 4 * Opioids, benzodiazepines, muscle relaxants, phenobarbital, and/or dilantin * Plasma creatinine of \>1 mg/dl * Severe cyanotic heart disease or severe respiratory distress * Abdominal wall or intestinal anomaly or injury (NEC) * Facial anomaly or other known chromosomal anomaly * Life-threatening congenital anomaly or are so critically ill that they are unlikely to survive or are receiving palliative care

Design outcomes

Primary

MeasureTime frameDescription
Stress biomarkersDay 3Compare group differences in measures of stress (i.e., salivary cortisol, urinary biomarkers of Hx, Xa, UA, and allantoin, and stress buffering (i.e., salivary oxytocin) between the intervention and usual care groups.

Secondary

MeasureTime frameDescription
Mother's Satisfaction with SSCDay 3Mother's Satisfaction with SSC Questionnaire
Number of discomforting and stressful events for motherDay 3Total count of discomfort and stressful events
Number of discomforting and stressful events for infantDay 3Total count of discomforting and stressful events
Change in stress biomarkerspre and post the intervention on days 1, 2, and 3salivary cortisol, urinary biomarkers of Hx, Xa, Uric Acid (UA), and allantoin and stress buffering (i.e., salivary oxytocin

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026