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Clinical Trials/NCT07548229
NCT07548229Active, not recruitingNot Applicable

Effect of Kangaroo Mother Care on Energy Utilization in Preterm Neonates

Ain Shams University1 site in 1 country60 target enrollmentStarted: May 15, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
60
Locations
1
Primary Endpoint
Urinary biomarkers of energy utilization

Study Overview

Brief Summary

This study aims to assess the impact of kangaroo mother care on energy utilization in preterm neonates by measuring urinary levels of xanthine, uric acid, and malondialdehyde.

It also aims to evaluate the effect of kangaroo mother care on physiological stress parameters in preterm neonates, as well as maternal emotional status

Detailed Description

This randomized controlled clinical trial aims to evaluate the effect of kangaroo mother care on energy utilization and oxidative stress in preterm neonates admitted to the neonatal intensive care unit (NICU) at Ain Shams University Children's Hospital, Cairo, Egypt.

Preterm neonates with gestational age between 32 and 36 weeks who meet the eligibility criteria will be enrolled and randomly assigned into two groups: an intervention group receiving kangaroo mother care and a control group receiving routine incubator care.

All enrolled neonates will receive routine incubator care until day 3 of life. On day 3, the intervention group will receive one hour of kangaroo mother care provided by the mother after feeding, while the control group will receive one hour of standard nursing care without kangaroo mother care.

Physiological parameters, including heart rate, respiratory rate, oxygen saturation, and temperature, will be monitored at baseline and every 15 minutes during the intervention period.

Urine samples will be collected from neonates 3 hours before and 3 hours after the intervention to measure biomarkers of energy utilization (xanthine and uric acid) and oxidative stress (malondialdehyde) using ELISA kits.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
1 Day to 1 Month (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Preterm neonates (32-36 weeks)
  • Vitally stable
  • On room air or low ventilatory support

Exclusion Criteria

  • Neonates requiring surgery
  • Intraventricular hemorrhage
  • Receiving sedatives (morphine, fentanyl, midazolam)
  • Renal impairment
  • Congenital anomalies
  • Cyanotic heart disease
  • Severe respiratory distress
  • Hemodynamic instability
  • Hypothermia
  • Parental refusal

Arms & Interventions

study group

Experimental

babies at day 3 will have kangro mother care

Intervention: kangroo mother care (Behavioral)

control group

Placebo Comparator

will have routine incubator care

Intervention: routine incubation care (Behavioral)

Outcomes

Primary Outcomes

Urinary biomarkers of energy utilization

Time Frame: 3 hours before and 3 hours after intervention on day 3 of life

Urinary xanthine and uric acid levels measured using ELISA kits.

Oxidative stress marker

Time Frame: 3 hours before and 3 hours after intervention on day 3 of life

Urinary malondialdehyde level measured using ELISA kits.

heart rate

Time Frame: Baseline and every 15 minutes during 1 hour intervention on day 3 of life

Heart rate measured using standard neonatal monitoring devices.

Respiratory rate

Time Frame: Baseline and every 15 minutes during 1 hour intervention on day 3 of life

Respiratory rate measured using standard neonatal monitoring devices.

temperature

Time Frame: Baseline and every 15 minutes during 1 hour intervention on day 3 of life

Body temperature measured using standard neonatal monitoring devices.

Secondary Outcomes

  • maternal emotional status(Time Frame: 3 hours before and 3 hours after intervention on day 3 of life)
  • maternal emotional status(: 3 hours before and 3 hours after intervention on day 3 of life)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Salwa Amin Abd Elhamid

assisstant prfessor

Ain Shams University

Study Sites (1)

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