Effect of Mother's Touch and Nurse's Therapeutic Touch on Pain Level and Crying Time During Heel Blood Collection
The Effect of Mother's Touch and Nurse's Therapeutic Touch on Pain Level and Crying Time During Heel Blood Collection in Newborns: A Randomized Controlled Study
1 other identifier
interventional
120
1 country
1
Brief Summary
This prospective study is planned as a randomized controlled study with the purpose of determining the effect of Mother's Touch and Nurse's Therapeutic Touch on pain levels and crying times by newborns during heel blood collection.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 4, 2023
CompletedFirst Submitted
Initial submission to the registry
April 1, 2024
CompletedFirst Posted
Study publicly available on registry
April 5, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 15, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
February 10, 2025
CompletedJuly 9, 2025
July 1, 2025
1.3 years
April 1, 2024
July 4, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
NIPS (Neonatal Infant Pain Scale)
It was developed in 1993 to evaluate interventional pain in newborns. Its Turkish adaptation was made in 1999. NIPS is an assessment tool that focuses on six behavioral responses of newborns: facial expressions, crying, breathing, arm movements, leg movements, and arousal. A score between 0 and 7 is obtained from the scale, and as the score obtained from the scale increases, the pain of newborns also increases. In the Turkish adaptation study of the scale, the Cronbach's alpha value was calculated as 0.83 before the procedure, 0.83 during the procedure and 0.86 after the procedure.
during the heel blood collection procedures (10 minutes)
Secondary Outcomes (2)
Crying times
during the heel blood collection procedures (average 10 minutes)
Processing time
during the heel blood collection procedures (average 10 minutes)
Study Arms (3)
Mother's Touch Group
EXPERIMENTALHeel blood will be taken while the infant was Mother's Touch. Mother's touch will be applied to the infants before, during and after the procedure.
Nurse's Therapeutic Touch Group
EXPERIMENTALHeel blood will be taken while the infant was Nurse's Therapeutic Touch.Therapeutic Touch will be applied to the infants before, during and after the procedure.
Control Group
NO INTERVENTIONIn this group, infants received routine heel blood collection procedure.
Interventions
Heel blood will be taken while the infant was Mother's Touch. Mother's touch will be applied to the infants before, during and after the procedure.
Heel blood will be taken while the infant was Nurse's Therapeutic Touch.Therapeutic Touch will be applied to the infants before, during and after the procedure.
Eligibility Criteria
You may qualify if:
- Parents who volunteered and gave consent to participate in the research
- Full term neonates (38-42 weeks of gestation)
- Underwent heel stick blood drawing for routine metabolic screening
- Aged 1 to 4 days
- Passed the hearing screening
- Birth weight between 2500-4400 grams
- Parents who know how to read, write and speak Turkish.
You may not qualify if:
- Parents with any mental problems
- Infants with any chronic disease and congenital anomalies.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Burdur Bucak State Hospital
Burdur, Bucak, 15030, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Selda Ateş Beşirik, PhD.
Burdur Mehmet Akif Ersoy University
- STUDY DIRECTOR
Emine Geçkil, Professor
Necmettin Erbakan University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
April 1, 2024
First Posted
April 5, 2024
Study Start
September 4, 2023
Primary Completion
December 15, 2024
Study Completion
February 10, 2025
Last Updated
July 9, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
Individual participant data that underlie the results reported in this study, after deidentification, will be shared with researchers who provide a methodologically sound proposal.