- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07651592
MOTHER3SENSE Study (MOTHER3SENSE)
Effects of Maternal Voice, Touch, and Scent on Pain and Stress in Newborns: A Comparison of Three Sensory Interventions
연구 개요
상세 설명
Painful procedures are frequently performed in newborns during routine clinical care and may lead to physiological and behavioral stress responses. Non-pharmacological interventions are recommended as safe and effective approaches for reducing procedural pain and stress in newborns. Maternal sensory stimuli, including maternal voice, touch, and scent, may provide comfort and support neonatal regulation during painful procedures.
This randomized controlled trial aims to compare the effects of maternal voice, maternal touch, and maternal scent on pain and stress responses in newborns undergoing a routine heel lance procedure. Eligible newborns will be randomly assigned to one of four groups: maternal voice, maternal touch, maternal scent, or control.
The assigned intervention will be applied according to a standardized protocol before, during, and after the heel lance procedure. Pain and stress responses will be assessed at three time points: before the procedure, during the procedure, and after the procedure. Behavioral and physiological indicators will be used to evaluate neonatal pain and stress responses.
The primary objective of the study is to determine and compare the effectiveness of maternal voice, touch, and scent in reducing procedural pain and stress in newborns. The findings may contribute to evidence-based, family-centered, and non-pharmacological pain management practices in neonatal care.
연구 유형
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Elif Simay KOÇ, Lecturer
- 전화번호: +90 348 813 93 01
- 이메일: kocelifsimay@gmail.com
연구 장소
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Kilis, 터키 (Türkiye), 79000
- Kilis Alaeddin Yavaşça State Hospital
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연락하다:
- Elif Simay KOÇ
- 전화번호: +90 348 813 93 01
- 이메일: kocelifsimay@gmail.com
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참여기준
자격 기준
공부할 수 있는 나이
- 어린이
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- Term newborns born between 37 and 42 weeks of gestation
- Newborns without respiratory, cardiac, metabolic, neurological, or infectious diseases
- Newborns not requiring oxygen therapy, phototherapy, or intravenous treatment
- Newborns scheduled to undergo a routine heel lance procedure (metabolic screening or blood sampling)
- Mothers willing to participate in the study
- Written informed consent provided by the parent or legal guardian
- Normal vital signs before the procedure (heart rate, respiratory rate, and oxygen saturation within normal limits)
Exclusion Criteria:
- Preterm (<37 weeks) or post-term (>42 weeks) newborns
- Presence of congenital anomalies or neurological disorders
- Requirement for oxygen therapy, phototherapy, or intravenous treatment
- Respiratory, cardiac, metabolic, neurological, or infectious disease
- Abnormal vital signs before the procedure
- Parent or legal guardian refusal to provide informed consent
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 방지
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: Maternal Voice
The recorded maternal voice will be presented to the newborn before, during, and after the procedure.
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The recorded maternal voice will be presented to the newborn before, during, and after the procedure.
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실험적: Maternal Touch
The mother will maintain contact with the newborn's palms before, during, and after the procedure to stimulate the grasp reflex and provide tactile sensory input.
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The mother will maintain contact with the newborn's palms before, during, and after the procedure to stimulate the grasp reflex and provide tactile sensory input.
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실험적: Maternal Scent
The newborn will be exposed to maternal breast milk scent during the procedure.
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The newborn will be exposed to maternal breast milk scent during the procedure.
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간섭 없음: Control
Routine heel lance procedures will be performed, and no sensory intervention will be provided.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Neonatal Infant Pain Scale
기간: Before the procedure, during the procedure, and immediately after the procedure
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The Neonatal Infant Pain Scale (NIPS), originally developed by Lawrence et al. (1993), was adapted into Turkish by Akdovan (Akdovan & Yıldırım, 1999).
NIPS is used to assess procedure-related pain in newborn infants.
The scale evaluates five behavioral indicators-facial expression, crying, arm movements, leg movements, and state of arousal-as well as one physiological parameter, breathing pattern.
Pain is assessed based on the evaluation of these behavioral and physiological responses.
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Before the procedure, during the procedure, and immediately after the procedure
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Newborn stress scale
기간: Before the procedure, during the procedure, and immediately after the procedure
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The Newborn Stress Scale (NSS), developed by Ceylan and Bolışık, consists of 24 items rated on a 3-point Likert scale.
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Before the procedure, during the procedure, and immediately after the procedure
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기타 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Newborn and Maternal Characteristics Form
기간: At baseline
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This researcher-developed form, based on the literature, was used to systematically collect demographic information about mothers and medical and birth-related characteristics of newborns.
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At baseline
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Neonatal Physiological Parameters Monitoring Form
기간: Before the procedure, during the procedure, and immediately after the procedure
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The Newborn Physiological Parameters Assessment Form was developed by the researchers based on the literature and was used to evaluate physiological parameters, including heart rate, oxygen saturation, and body temperature, before, during, and after the heel lance procedure.
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Before the procedure, during the procedure, and immediately after the procedure
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공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
- Kilis 7 Aralık Universty
- MOTHER3SENSE Study (기타 식별자: Kilis 7 Aralık Universty)
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
스트레스, 심리적에 대한 임상 시험
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Goethe UniversityLudwig-Maximilians - University of Munich완전한
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Maternal Voice에 대한 임상 시험
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University of Wisconsin, MadisonNational Heart, Lung, and Blood Institute (NHLBI)완전한
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The Hong Kong Polytechnic UniversityNethersole Institute of Continuing Holistic Health Education (NICHE)완전한
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Duke-NUS Graduate Medical SchoolNational Kidney Foundation, Singapore모병
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Celal Bayar University아직 모집하지 않음
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Stanford UniversityNational Institute on Aging (NIA)모집하지 않고 적극적으로
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University of TennesseeNational Cancer Institute (NCI); University of Alabama at Birmingham완전한
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University of FloridaNational Institute on Alcohol Abuse and Alcoholism (NIAAA)모병