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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04368767
Other study ID # 19-29543
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 3, 2020
Est. completion date September 30, 2020

Study information

Verified date November 2020
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date September 30, 2020
Est. primary completion date September 30, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility 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

Study Design


Intervention

Behavioral:
Skin-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.

Locations

Country Name City State
United States UCSF Benioff Children's Hospital San Francisco San Francisco California

Sponsors (1)

Lead Sponsor Collaborator
University of California, San Francisco

Country where clinical trial is conducted

United States, 

References & Publications (9)

Blass E. Energy conservation in infants. Behav Processes. 2015 Aug;117:35-41. doi: 10.1016/j.beproc.2015.01.011. Epub 2015 Jan 30. — View Citation

Chi Luong K, Long Nguyen T, Huynh Thi DH, Carrara HP, Bergman NJ. Newly born low birthweight infants stabilise better in skin-to-skin contact than when separated from their mothers: a randomised controlled trial. Acta Paediatr. 2016 Apr;105(4):381-90. doi — View Citation

Cong X, Ludington-Hoe SM, Hussain N, Cusson RM, Walsh S, Vazquez V, Briere CE, Vittner D. Parental oxytocin responses during skin-to-skin contact in pre-term infants. Early Hum Dev. 2015 Jul;91(7):401-6. doi: 10.1016/j.earlhumdev.2015.04.012. Epub 2015 Ma — View Citation

Isayama T, Lewis-Mikhael AM, O'Reilly D, Beyene J, McDonald SD. Health Services Use by Late Preterm and Term Infants From Infancy to Adulthood: A Meta-analysis. Pediatrics. 2017 Jul;140(1). pii: e20170266. doi: 10.1542/peds.2017-0266. Review. — View Citation

Kim KM, Henderson GN, Ouyang X, Frye RF, Sautin YY, Feig DI, Johnson RJ. A sensitive and specific liquid chromatography-tandem mass spectrometry method for the determination of intracellular and extracellular uric acid. J Chromatogr B Analyt Technol Biome — View Citation

Mörelius E, He HG, Shorey S. Salivary Cortisol Reactivity in Preterm Infants in Neonatal Intensive Care: An Integrative Review. Int J Environ Res Public Health. 2016 Mar 18;13(3). pii: E337. doi: 10.3390/ijerph13030337. Review. — View Citation

Plank MS, Calderon TC, Asmerom Y, Boskovic DS, Angeles DM. Biochemical measurement of neonatal hypoxia. J Vis Exp. 2011 Aug 24;(54). pii: 2948. doi: 10.3791/2948. — View Citation

Tan JBC, Boskovic DS, Angeles DM. The Energy Costs of Prematurity and the Neonatal Intensive Care Unit (NICU) Experience. Antioxidants (Basel). 2018 Mar 2;7(3). pii: E37. doi: 10.3390/antiox7030037. Review. — View Citation

Tolun AA, Zhang H, Il'yasova D, Sztáray J, Young SP, Millington DS. Allantoin in human urine quantified by ultra-performance liquid chromatography-tandem mass spectrometry. Anal Biochem. 2010 Jul 15;402(2):191-3. doi: 10.1016/j.ab.2010.03.033. Epub 2010 M — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Stress biomarkers 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. Day 3
Primary Stress biomarkers 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. Day 2
Primary Stress biomarkers 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. Day 1
Secondary Mother's Satisfaction with SSC Mother's Satisfaction with SSC Questionnaire Day 3
Secondary Number of discomforting and stressful events for mother Total count of discomfort and stressful events Day 3
Secondary Number of discomforting and stressful events for mother Total count of discomfort and stressful events Day 2
Secondary Number of discomforting and stressful events for mother Total count of discomfort and stressful events Day 1
Secondary Number of discomforting and stressful events for infant Total count of discomforting and stressful events Day 3
Secondary Number of discomforting and stressful events for infant Total count of discomforting and stressful events Day 2
Secondary Number of discomforting and stressful events for infant Total count of discomforting and stressful events Day 1
Secondary Change in stress biomarkers salivary cortisol, urinary biomarkers of Hx, Xa, Uric Acid (UA), and allantoin and stress buffering (i.e., salivary oxytocin pre and post the intervention on days 1, 2, and 3
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