NCT05797532

Brief Summary

Newborns are exposed to painful invasive procedures from the first hours of their lives. It is stated that the functional and anatomical structure of the neural pathways of newborns with many systems immature develops well enough to feel pain and they have the ability to remember after experiencing pain. Physiological symptoms (increase in heart rate and blood pressure, increase in oxygen saturation, etc.) as a result of painful procedures (vascular or heel lance collection, venous or arterial catheterization, subcutaneous and intramuscular injection, chest tube insertion, intubation, aspiration, etc.) applied for diagnosis and treatment in newborns. falling), crying behavior and metabolic problems. In conclusion, the energy resources required for the growth and development of newborns are used to cope with pain, and it is reported that repetitive painful procedures increase mortality and morbidity in newborns. Heel lance, which is applied to all newborns within the scope of the newborn screening program, is one of the painful invasive procedures for newborns. Heel lance should be taken as capillaries in the first 48 hours after feeding or until the first week of life of newborns. In the literature, non-pharmacological methods applied to reduce the severity of pain felt by newborns during heel lance, which also causes tissue integrity deterioration; It has been observed that studies examining the effects of breast milk, swaddling, holding, breastfeeding, music, oral sucrose, non-nutritive sucking, skin-to-skin contact (SSC) and positioning. SSC, breastfeeding and swaddling + holding methods are among the methods that can be easily used by mothers and nurses. Nurses working in the maternity ward where heel lance sampling is performed in the hospital have a key role in reducing the pain level of newborns by collaborating with the families of the babies.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
90

participants targeted

Target at P50-P75 for not_applicable pain

Timeline
Completed

Started Nov 2019

Shorter than P25 for not_applicable pain

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 18, 2019

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 31, 2020

Completed
2.6 years until next milestone

First Submitted

Initial submission to the registry

December 21, 2022

Completed
3 months until next milestone

First Posted

Study publicly available on registry

April 4, 2023

Completed
Last Updated

April 4, 2023

Status Verified

December 1, 2022

Enrollment Period

7 months

First QC Date

December 21, 2022

Last Update Submit

April 2, 2023

Conditions

Keywords

heel lancebreastfeedingswaddling and holdingskin to skin contact

Outcome Measures

Primary Outcomes (1)

  • Determination of pain scores according to measurement times; before the heel lance procedure, the newborn was 5 minutes after breastfeeding, swaddling and holding, skin-to-skin contact.

    Neonatal Infant Pain Scale pain score of the newborn were recorded by the researcher in the breastfeeding, swaddling and holding, skin-to skin-contact groups, 2 minutes before the heel lance, 10 seconds during the heel lance, and 2 minutes after the heel lance was completed. The lowest score obtained from the scale is 0, and the highest score is 7. A high scale score indicates a high level of pain in the newborn. The scoring of Neonatal Infant Pain Scale ranges from 0-7 points and 0-2 points indicate no pain, 3-4 points indicate moderate pain, \>4 points indicate high levels of pain.

    through study completion, an average of 6 month

Study Arms (3)

breastfeeding

ACTIVE COMPARATOR

The mother was allowed to sit comfortably in the patient's room, the pulse oximeter probe was attached to the left foot of the newborn, and the newborn, who was placed on the mother's lap, was breastfeeding for 5 minutes before the heel lance, and breastfeeding was continued during the procedure.

Other: breastfeeding

skin to skin contact

ACTIVE COMPARATOR

The newborn's clothes were removed so that only the diaper and baby hat were left, and a pulse oximeter probe was attached to his left foot. The newborn was placed on the mother's bare chest between her two breasts, facing the mother's face, with her head up, in the prone position, covered with a baby blanket, and skin-to-skin contact was made between the mother and the newborn for at least 5 minutes before starting the heel lance procedure.

Other: skin to skin contact

swaddling and holding

ACTIVE COMPARATOR

A pulse oximeter probe was attached to the newborn's left foot, and the legs were in flexion and abduction position, wrapped with a square cloth blanket and placed on his mother's lap. It was ensured that the newborn was held in the mother's lap with his head up and feet down for 5 minutes before heel lance.

Other: swaddling and holding

Interventions

The NIPS (Neonatal Infant Pain Scale) pain score, heart rate and oxygen saturation of the newborn were recorded by the researcher in the study group, 2 minutes before the heel lance, 10 seconds during the heel lance, and 2 minutes after the heel lance was completed. In order to determine the crying time of newborns in all three study groups, the voice recorder and stopwatch were turned on two minutes before and 2 minutes after the heel lance.

breastfeeding

The NIPS (Neonatal Infant Pain Scale) pain score, heart rate and oxygen saturation of the newborn were recorded by the researcher in the study group, 2 minutes before the heel lance, 10 seconds during the heel lance, and 2 minutes after the heel lance was completed. In order to determine the crying time of newborns in all three study groups, the voice recorder and stopwatch were turned on two minutes before and 2 minutes after the heel lance.

skin to skin contact

The NIPS (Neonatal Infant Pain Scale) pain score, heart rate and oxygen saturation of the newborn were recorded by the researcher in the study group, 2 minutes before the heel lance, 10 seconds during the heel lance, and 2 minutes after the heel lance was completed. In order to determine the crying time of newborns in all three study groups, the voice recorder and stopwatch were turned on two minutes before and 2 minutes after the heel lance.

swaddling and holding

Eligibility Criteria

Age24 Hours - 36 Hours
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • Newborns (0-28days);
  • Being born at term (38 - 42 weeks)
  • Stable vital signs
  • Having completed the first 24 hours of life and being fed
  • Heel blood procedure will be applied for the Ministry of Health screening.
  • Not being breastfed 30 minutes before the procedure
  • No previous invasive intervention other than vitamin K and hepatitis B vaccine.
  • st and 5th minute Apgar score ≥7
  • Parents have given written consent.

You may not qualify if:

  • Newborns (0-28days);
  • Unstable vital signs
  • Being bottle-fed or formula-fed
  • Having a neurological diagnosis
  • Prior exposure to another invasive procedure other than vitamin K and hepatitis B vaccine.
  • Maternal use of opioids,
  • Not being born at term.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kutahya Health Sciences University

Kütahya, Turkey (Türkiye)

Location

Related Publications (1)

  • Karga Yilmaz T, Yavuz B. Comparison of different methods for reducing pain during a heel lance in newborns: a randomized trial. Ital J Pediatr. 2025 Mar 12;51(1):73. doi: 10.1186/s13052-025-01916-w.

MeSH Terms

Conditions

PainBreast Feeding

Interventions

Lactation

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsFeeding BehaviorBehavior

Intervention Hierarchy (Ancestors)

Reproductive Physiological PhenomenaReproductive and Urinary Physiological PhenomenaPostpartum Period

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Model Details: Comparison of three different methods
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 21, 2022

First Posted

April 4, 2023

Study Start

November 18, 2019

Primary Completion

May 31, 2020

Study Completion

May 31, 2020

Last Updated

April 4, 2023

Record last verified: 2022-12

Locations