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Clinical Trials/NCT00776789
NCT00776789
Completed
Not Applicable

Effect of Early Skin to Skin Contact on Breast Feeding Behaviour in Term Newborns: A Randomized Controlled Trial

All India Institute of Medical Sciences, New Delhi1 site in 1 country41 target enrollmentAugust 2008
ConditionsBreastfeeding

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breastfeeding
Sponsor
All India Institute of Medical Sciences, New Delhi
Enrollment
41
Locations
1
Primary Endpoint
The Median Breast Feeding Score
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

Aims and Objectives

Aim

To determine the effect of delivery room Skin To Skin contact on breast feeding behavior of term neonates born by normal vaginal delivery at 36-48 hours.

Objectives Primary objective To determine the effect of delivery room Skin To Skin contact on breast feeding behaviour of term neonates born by normal vaginal delivery, between 36-48 hours (as measured by Infant Breast Feeding Score) by video recording using a randomized controlled design.

Secondary objectives To determine the effect of delivery room Skin to Skin contact on

  1. Salivary cortisol at 6 hours as measured by electrochemiluminescence immunoassay (ECLIA)
  2. Weight at 48 hours as measured by digital infant weighing scale.
  3. Maternal perception of breast milk output, breast consistency, infant's feeding and activity at 36-48 hours as measured by a score graded as very satisfied, satisfied, acceptable and not satisfied.
  4. Number and duration of feeding sessions till 48 hrs according to the mother as assessed at 48 hours
  5. Breast feeding rates at 6 weeks measured at the time of vaccination at the time of visit to the hospital for the same or as asked by telephonic conversation.

Hypothesis

Infants receiving skin to skin contact when compared with neonates not receiving it, demonstrate better breast feeding behaviour.

Detailed Description

Inclusion and exclusion criteria for the enrollment of subjects in the study Inclusion criteria Term babies born to mothers by normal vaginal delivery in the study period. Exclusion criteria 1. Babies with major congenital malformation. 2. Multiple pregnancy 3. Babies requiring resuscitation beyond the initial steps 4. Babies requiring care in the neonatal intensive care unit. 5. Maternal problems requiring immediate care * Severe preeclampsia defined as Blood pressure more than 160/110, Proteinuria more than 3+, Oliguria less than 500 ml, Pulmonary edema, cerebral visual disturbances, Impaired liver function, Thrombocytopenia, Epigastric Pain * Imminent eclampsia * Severe bleeding * Mother with significant surgical or medical illness requiring separation of the baby from the mother. 6. Small for dates and large for dates babies 7. Infants of diabetic mother 8. Maternal refusal of consent Outcome Measures: 1. Measurement of Breast feeding Behavior at 36-48 hours using Infant Breast feeding Behavior scale 2. Salivary Cortisol 3. Weight at birth 4. Weight at 48 hours 5. Number of feeding sessions till 48 hours 6. Maternal Perception of Infant activity, feeding and breast milk output.

Registry
clinicaltrials.gov
Start Date
August 2008
End Date
June 2009
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
All India Institute of Medical Sciences, New Delhi
Responsible Party
Principal Investigator
Principal Investigator

Anu Thukral

Doctor

All India Institute of Medical Sciences, New Delhi

Eligibility Criteria

Inclusion Criteria

  • Term babies born to mothers by normal vaginal delivery in the study period.

Exclusion Criteria

  • Babies with major congenital malformation.
  • Multiple pregnancy
  • Babies requiring resuscitation beyond the initial steps
  • Babies requiring care in the neonatal intensive care unit.
  • Maternal problems requiring immediate care
  • Severe preeclampsia defined as Blood pressure more than 160/110, Proteinuria more than 3+, Oliguria less than 500 ml, Pulmonary edema, cerebral visual disturbances, Impaired liver function, Thrombocytopenia, Epigastric Pain
  • Imminent eclampsia
  • Severe bleeding
  • Mother with significant surgical or medical illness requiring separation of the baby from the mother.
  • Small for dates and large for dates babies

Outcomes

Primary Outcomes

The Median Breast Feeding Score

Time Frame: 36-48 hours by video recording

This was a one point assessment done at 36-48 hours by video recording. The video recording was carried out in a separate well lighted room after taking informed consent from the mother. The mother had full right to see the video and only if she was satisfied, was then the video finally stored. These videos were analyzed later using the infant breast feeding assessment tool : a scoring measure \[0 to 3\] for i) readiness to feed ii) sucking iii) rooting and iv) latching. The total possible score could vary from 0 to 12, with 12 being the best possible total score. Successful breastfeeding was defined as a total score of more \>=8.

Secondary Outcomes

  • Breast Feeding Status at 48 Hours(48 hours)
  • Salivary Cortisol(6 hours)
  • Breast Feeding Status at 6 Weeks(6 weeks)

Study Sites (1)

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