- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06886412
Non-Pharmacological Methods for Reducing Pain During Vaccination in Infants
July 13, 2025 updated by: Emel AVÇİN, University of Yalova
The Effect of Breastfeeding and Maternal Holding on Reducing Pain During Vaccination in Infants
Pain management in infants is a medical responsibility of all members of the healthcare team, and nurses hold a privileged role in this regard.
The primary goal of pain management is to accurately assess and identify the infant's pain at an early stage, support the development of coping mechanisms through both pharmacological and non-pharmacological methods, and minimize the pain experience as much as possible.
Pain management achieved through non-pharmacological interventions constitutes a safe, non-invasive, cost-effective, and independently performed nursing practice.
This randomized controlled study was conducted to determine the effect of non-pharmacological methods, specifically maternal holding and breastfeeding, on reducing pain during vaccination in infants.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
90
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Yalova, Turkey, 77200
- Yalova University
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being healthy,
- Aged between 4 weeks and 6 months,
- Parents have given verbal and written consent to participate in the study,
- Born at term (37 weeks of gestation or later),
- Scheduled for vaccination under the Ministry of Health's vaccination program,
- Not having taken analgesics/antipyretics in the last 4 hours before the procedure,
- Having a normal body temperature (between 36.5°C and 37.1°C).
Exclusion Criteria:
- Having a chronic or mental illness, or a congenital anomaly,
- Being older than 6 months,
- Having a body temperature above 37.1°C,
- Receiving analgesics, sedatives, or any other medication.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Maternal Holding Group
Five minutes before the vaccination procedure, the infant will be handed to the mother in a position suitable for vaccination and will remain in her arms throughout the procedure.
It will be checked that the infant's diaper has been changed..The mother will be informed about the importance of stabilizing the leg to be vaccinated during the procedure and will be instructed to hold the infant in a comfortable position.
The mother will hold the infant in her lap, using one arm and hand to secure the infant's arms and the other arm and hand to hold the infant's legs.
The infant's pain level will be assessed using the Neonatal Infant Pain Scale (NIPS) before, during, and after the vaccination procedure.
Crying duration will be measured using a mobile phone stopwatch and recorded in the application record form.
The final NIPS assessment and crying duration measurement will be performed 3 minutes after the procedure.
|
The infant is required to be held in the mother's arms before, during, and after the procedure.
The maternal holding method will be shown or explained to the mother by the researchers.
|
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Experimental: Breast Feeding Group
Before the vaccination procedure, the infant and mother will be taken to the vaccination room.
The infant's diaper will be checked to ensure it has been changed.
The mother will be asked whether the infant has been fed at least 30 minutes before the procedure.
The mother will be instructed to sit comfortably on the examination table with her back supported against the wall.
The mother will then take the infant in her arms, and the infant will be placed in a cradle hold breastfeeding position.
The infant will be handed to the mother 2 minutes before the procedure, and breastfeeding will begin.
The infant's pain level will be assessed using the Neonatal Infant Pain Scale (NIPS) before, during, and after the vaccination procedure.
Crying duration will be measured using a mobile phone stopwatch and recorded in the application record form.
The final NIPS assessment and crying duration measurement will be performed 3 minutes after the procedure.
|
The infant's mother is instructed to begin breastfeeding 2 minutes before the procedure, continuing during and after the procedure.
The breastfeeding position for the infant will be shown or explained to the mother by the researchers.
|
|
No Intervention: Control Group
The infants in the control group will receive their vaccinations in the same manner as routine vaccination procedures.
Before the vaccination procedure, the infant and their parent will be taken to the room where the procedure will take place, and the infant will be laid on the examination table.
During the procedure, the mother will remain next to her infant.
To restrict the movement of the infant's legs during the vaccination, the nurse will stabilize the infant's leg with one hand while performing the procedure with the other hand.
No non-pharmacological methods will be applied during the procedure.
The infant's pain level will be assessed using the Neonatal Infant Pain Scale (NIPS) before, during, and after the vaccination.
Crying duration will be measured using a mobile phone stopwatch and recorded in the application record form.
The final NIPS assessment and crying duration measurement will be performed 3 minutes after the procedure.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluation of pain and crying duration in the infant held in the mother's arms during the vaccination procedure
Time Frame: Two minutes before the procedure, during the procedure, and three minutes after the procedure.
|
The pain of the infant held in the mother's arms will be measured using the Neonatal Infant Pain Scale 2 minutes before the procedure, during the procedure, and 3 minutes after the procedure.
The crying duration before and after the procedure will be measured using a stopwatch.
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Two minutes before the procedure, during the procedure, and three minutes after the procedure.
|
|
Evaluation of pain and crying duration in the infant held in the breast feeding during the vaccination procedure
Time Frame: Two minutes before the procedure, during the procedure, and three minutes after the procedure.
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The pain of the infant using the breastfeeding method will be measured using the Neonatal Infant Pain Scale 2 minutes before the procedure, during the procedure, and 2 minutes after the procedure.
The crying duration before and after the procedure will be measured using a stopwatch.
|
Two minutes before the procedure, during the procedure, and three minutes after the procedure.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: EMEL AVÇİN, Doctor, University of Yalova
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 2, 2025
Primary Completion (Actual)
April 4, 2025
Study Completion (Actual)
April 25, 2025
Study Registration Dates
First Submitted
March 14, 2025
First Submitted That Met QC Criteria
March 14, 2025
First Posted (Actual)
March 20, 2025
Study Record Updates
Last Update Posted (Actual)
July 15, 2025
Last Update Submitted That Met QC Criteria
July 13, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Emel Avcin Pain
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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