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Completed

NCT Number: NCT04368767

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

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.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UCSF Benioff Children's Hospital San Francisco

San Francisco, California, 94158, United States

Who can participate

Healthy volunteers accepted: Yes

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

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

Treatment and study plan

Skin-to-skin

Behavioral

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.

Primary outcomes

  1. Stress biomarkers

    Time frame: Day 3

    Compare 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.

  2. Stress biomarkers

    Time frame: Day 2

    Compare 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.

  3. Stress biomarkers

    Time frame: Day 1

    Compare 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 outcomes

  1. Mother's Satisfaction with SSC

    Time frame: Day 3

    Mother's Satisfaction with SSC Questionnaire

  2. Number of discomforting and stressful events for mother

    Time frame: Day 3

    Total count of discomfort and stressful events

  3. Number of discomforting and stressful events for mother

    Time frame: Day 2

    Total count of discomfort and stressful events

  4. Number of discomforting and stressful events for mother

    Time frame: Day 1

    Total count of discomfort and stressful events

  5. Number of discomforting and stressful events for infant

    Time frame: Day 3

    Total count of discomforting and stressful events

  6. Number of discomforting and stressful events for infant

    Time frame: Day 2

    Total count of discomforting and stressful events

  7. Number of discomforting and stressful events for infant

    Time frame: Day 1

    Total count of discomforting and stressful events

  8. Change in stress biomarkers

    Time frame: pre and post the intervention on days 1, 2, and 3

    salivary cortisol, urinary biomarkers of Hx, Xa, Uric Acid (UA), and allantoin and stress buffering (i.e., salivary oxytocin

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Registry information

Official study title

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

Acronym: PRCTS2S

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Apr 30, 2020
Registry last updated
Nov 12, 2020

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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