NCT06350084

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

87
On Track

Trial Health Score

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

Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2023

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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 4, 2023

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

April 1, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

April 5, 2024

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 15, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 10, 2025

Completed
Last Updated

July 9, 2025

Status Verified

July 1, 2025

Enrollment Period

1.3 years

First QC Date

April 1, 2024

Last Update Submit

July 4, 2025

Conditions

Keywords

NewbornPainTherapeutic TouchTouchHeel Stick

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

EXPERIMENTAL

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.

Behavioral: Mother's Touch

Nurse's Therapeutic Touch Group

EXPERIMENTAL

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.

Behavioral: Nurse's Therapeutic Touch

Control Group

NO INTERVENTION

In this group, infants received routine heel blood collection procedure.

Interventions

Mother's TouchBEHAVIORAL

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.

Mother's Touch Group

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.

Nurse's Therapeutic Touch Group

Eligibility Criteria

Age2 Days - 4 Days
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

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)

Location

MeSH Terms

Conditions

Acute PainCryingPain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsNonverbal CommunicationCommunicationBehavior

Study Officials

  • Selda Ateş Beşirik, PhD.

    Burdur Mehmet Akif Ersoy University

    PRINCIPAL INVESTIGATOR
  • Emine Geçkil, Professor

    Necmettin Erbakan University

    STUDY DIRECTOR

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

Individual participant data that underlie the results reported in this study, after deidentification, will be shared with researchers who provide a methodologically sound proposal.

Shared Documents
STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE

Locations