跳至主要内容
临床试验/NCT05079594
NCT05079594已完成不适用

Investigation of Infant Comfort Levels and Mothers' Anxiety Levels in Non-pharmacological Maternal Voice and White Noise Methods in Heel Blood Procedure

Akdeniz University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年3月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
CONFORTneo Scale

研究概览

简要总结

The heel blood procedure for newborn screening is done for almost all babies within the first 48 hours of birth. It is stated that non-pharmacological methods in reducing pain during the heel blood collection process are simple, effective, free, and very cost-effective. Studies have shown that auditory interventions (such as mother's voice, white noise) used in invasive procedures distract the infant and create a cognitive strategy for pain control. According to this information, one aim of the study is to determine the effect of the mother's voice and white noise, which are non-pharmacological methods, on the comfort level of the baby in the heel blood procedure. It is thought that especially acute painful procedures applied to infants will reduce the level of stress and anxiety in parents. Another aim of this study is to determine the effect of a mother's voice and white noise, which are non-pharmacological methods, on the state anxiety levels of mothers in the heel blood collection process.

详细描述

The heel blood procedure for newborn screening is done for almost all babies within the first 48 hours of birth. The heel blood procedure, which is widely used for the diagnosis and follow-up of various diseases, causes acute pain in infants. It is stated that non-pharmacological methods in reducing pain during the heel blood collection process are simple, effective, free, and very cost-effective. For example, non-pharmacological methods such as breastfeeding, skin-to-skin contact, oral sucrose, mother's voice, and white noise are stated to be effective in reducing acute pain. Clinical practice guidelines recommend the use of non-pharmacological methods in acute painful procedures. Studies have shown that auditory interventions (such as mother's voice, white noise) used in invasive procedures distract the infant and create a cognitive strategy for pain control. According to this information, one aim of the study is to determine the effect of the mother's voice and white noise, which are non-pharmacological methods, on the comfort level of the baby in the heel blood procedure.

Few studies have targeted parents of newborn infants, although studies to date have shown that parents want to be more involved in their infants' pain management. Parents reported that they wanted to learn more about pain management strategies, they wanted to play a role in the relaxation of their babies, and they hoped for more opportunities to participate in the care of their babies in the hospital. It is thought that especially acute painful procedures applied to infants will reduce the level of stress and anxiety in parents. In addition, one study reported that when parents are given information to help reduce their baby's pain, they accept painful procedures such as heel prick more easily and feel calmer. In the light of this information, another aim of this study is to determine the effect of a mother's voice and white noise, which are non-pharmacological methods, on the state anxiety levels of mothers in the heel blood collection process.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
1 Hour 至 1 Month(Child)
性别
All
接受健康志愿者

入选标准

  • Newborns whose postnatal age is between 1-5 days,
  • newborns born between gestational weeks,
  • Healthy newborns,
  • Babies of mothers without diabetes,
  • Newborns who were not given any opioid and non-opioid drugs before the application,
  • Newborns who have been fed at least 30 minutes ago,
  • Newborns without any painful interventions other than vitamin K and Hepatitis B injections will be included.
  • Mothers who can speak and understand Turkish,
  • The mothers and their babies who accepted to participate in the study and whose written consent form was obtained from them will be included in the study.

排除标准

  • Connected to a mechanical ventilator,
  • Having a neurological disorder,
  • Congenital anomaly,
  • Having hyperglycemia,
  • Having undergone a surgical procedure,
  • Substance addicted mother and her baby,
  • If the lancet cannot be inserted and removed at once, the baby will be excluded from the study.
  • Infants, despite meeting the criteria, will be excluded from the study if the heel blood collection takes more than 2 minutes in total, the procedure is disrupted by someone entering the room loudly, or the mother changes the position of the baby.
  • Mothers with a special condition that will cause difficulties in understanding and perception will be excluded from the study.

研究组 & 干预措施

Routine Care Group

No Intervention

Before the application, the families will be informed by the researcher and the 'Informed Consent Form' will be signed. After the heel blood procedure, when the baby starts to cry, comfort will be provided with gentle touches. For ethical reasons, routine care will be provided when the baby cries.

White Noise

Experimental

Since white noise is a humming and continuous monotonous sound, it is similar to the sound in the womb. It will be explained that this sound is very similar to the sound that the baby hears in the mother's womb by making the white noise recordings listen to the mothers who will have their babies listen to white noise. by Orhan Osman; Dr. From the album 'Kolik', which was created by making use of the album 'The Happiest Baby' prepared by Harvey Karp, which consists only of uterus sounds; The song 'Don't Let Your Baby Cry, PT.2' will be played to babies. In addition, infants will be excluded from the study even though they meet the criteria, if they are not sedated, the procedure takes more than 2 minutes, the procedure is disrupted because someone enters the room loudly, or the mother changes the baby's position.

干预措施: White noise (Other)

Mother Voice

Experimental

Auditory responses, fetal age 26-28. It develops in the auditory cortex and brain stem in weeks. Hearing is one of the first senses a fetus develops and is 24-33. can recognize and remember the mother's voice after weeks. The fetus memorizes the musical characteristics of the mother's voice, like tone, by listening to it. It is stated that newborns exposed to their own mother's voice have a lower heart rate, higher sucking rate, a more relaxed appearance, and less crying and body movements.

干预措施: Mother voice (Other)

结局指标

主要结局

CONFORTneo Scale

时间窗: 1 year

The Neonatal Comfort Behavior Scale consists of 7 items: muscle tone, alertness, facial tension, calmness/agitation, body movements, respiratory response, and crying. Since "respiratory response" was scored in infants connected to mechanical ventilator and "crying" was scored in spontaneously breathing infants, the total score was calculated over 6 items. The lowest score that can be obtained from the Newborn Comfort Behavior Scale is 6, and the highest score is 30.On this scale, if the total score of the scale is between 6-13, the baby is comfortable. If the total score is between 14-30, the baby has pain or distress and needs interventions to relieve him.

次要结局

  • Heart rate peak(1 year)
  • Oxygen saturation(1 year)
  • State Anxiety Scale score(1 year)
  • Crying time(1 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Uğur Gül

Research Assistant

Akdeniz University

研究点 (1)

Loading locations...

相似试验

已完成
不适用
Caring for Babies During the Newborn Screening Blood TestPain
NCT02608892Children's Hospital of Eastern Ontario100
Unknown
不适用
Caring for Babies: A Study of Ontario Maternal-Newborn Hospitals on the Implementation of Parent-targeted EducationPain
NCT03099252Children's Hospital of Eastern Ontario8
进行中(未招募)
不适用
Early Check: Expanded Screening in NewbornsAdrenocorticotropic Hormone DeficiencyThyroid Dyshormonogenesis 3Hemophilia AAcrodermatitis EnteropathicaN-acetylglutamate Synthase DeficiencyCanavan DiseaseLiddle SyndromeOrnithine Transcarbamylase DeficiencyBiotinidase DeficiencyBeta-ketothiolase DeficiencyMaple Syrup Urine Disease, Type 1ANeonatal Severe Primary HyperparathyroidismIntrinsic Factor DeficiencyCerebrotendinous XanthomatosesMaple Syrup Urine Disease, Type 2Thyroid Dyshormonogenesis 5Supravalvar Aortic StenosisTyrosinemia, Type IGlycogen Storage Disease Type IGalactokinase DeficiencyGuanidinoacetate Methyltransferase DeficiencyMitochondrial Trifunctional Protein DeficiencyIsovaleric AcidemiaSevere Combined Immunodeficiency T-Cell Negative B-Cell Positive Due to Janus Kinase-3 Deficiency (Disorder)Diabetes Mellitus, Permanent Neonatal, With Neurologic Features3-Methylcrotonyl CoA Carboxylase 2 DeficiencyMethylmalonic Aciduria and Homocystinuria Type cblCCongenital Disorder of Glycosylation Type 1BMethylcobalamin Deficiency Type Cbl G (Disorder)Severe Combined Immunodeficiency Due to RAG2 DeficiencyThyroid Dyshormonogenesis 2ACarbonic Anhydrase VA DeficiencySevere Combined Immunodeficiency Due to Adenosine Deaminase DeficiencyPrimary Hyperoxaluria Type 1Pyridoxine-Dependent EpilepsyWilson DiseaseCarbamoyl Phosphate Synthetase I Deficiency DiseaseCarnitine Palmitoyl Transferase 1A DeficiencyCarnitine Palmitoyltransferase II DeficiencySevere Combined Immunodeficiency Due to DCLRE1C DeficiencyMucopolysaccharidosis Type IV AGtp Cyclohydrolase I DeficiencyJervell and Lange-Nielsen Syndrome 2Hyperinsulinemic Hypoglycemia, Familial, 2MAHCDMthfr DeficiencyGlycogen Storage Disease IXBThyroid Dyshormonogenesis 1Waardenburg Syndrome, Type 2ETranscobalamin II DeficiencyHypothyroidism Due to TSH Receptor MutationsHemophilia BChronic Granulomatous DiseaseFragile X SyndromeHyperargininemiaArgininosuccinic AciduriaCitrullinemia, Type IAlport Syndrome, Autosomal RecessiveFructose 1,6 Bisphosphatase DeficiencyHyperinsulinism-Hyperammonemia Syndrome3-Hydroxyacyl-CoA Dehydrogenase DeficiencyPrimary Hyperoxaluria Type 3Hermansky-Pudlak Syndrome 4Mucopolysaccharidosis Type 2Severe Combined Immunodeficiency Due to IL-7Ralpha DeficiencyCblFWaardenburg Syndrome Type 2AWaardenburg Syndrome Type 1Hereditary Hypophosphatemic RicketsEpilepsy, Early-Onset, Vitamin B6-DependentDihydropteridine Reductase DeficiencyMultiple Endocrine Neoplasia Type 2BBiotin-Responsive Basal Ganglia DiseaseGSD1CSRDUsher Syndrome Type 1CUsher Syndrome Type 1G (Diagnosis)Von Willebrand Disease, Type 3Developmental and Epileptic Encephalopathy 2Smith-Lemli-Opitz SyndromeRett SyndromeNiemann-Pick Disease, Type C1Leber Congenital Amaurosis 2Dravet SyndromeCreatine Transporter DeficiencyGlycogen Storage Disease, Type IXA2RetinoblastomaAngelman SyndromeLysosomal Acid Lipase DeficiencyHyperinsulinemic Hypoglycemia, Familial 1Congenital Bile Acid Synthesis Defect Type 2Mucopolysaccharidosis Type 6Factor X DeficiencyGlutaryl-CoA Dehydrogenase DeficiencyPrimary Hyperoxaluria Type 2Apparent Mineralocorticoid ExcessHSDBCBAS1Jervell and Lange-Nielsen Syndrome 1Methylmalonic Aciduria cblA TypeUsher Syndrome, Type 1FPyridoxal Phosphate-Responsive SeizuresPituitary Hormone Deficiency, Combined, 1Severe Combined Immunodeficiency Due to RAG1 DeficiencyRiboflavin Transporter DeficiencyBarth SyndromeSegawa Syndrome, Autosomal RecessiveAutosomal Recessive Nonsyndromic Hearing LossAdenine Phosphoribosyltransferase DeficiencyMolybdenum Cofactor Deficiency, Type A3-Phosphoglycerate Dehydrogenase DeficiencyNiemann-Pick Disease Type ATransient Neonatal Diabetes MellitusCentral Hypoventilation Syndrome With or Without Hirschsprung DiseaseDuchenne Muscular DystrophyFragile X - PremutationAdrenoleukodystrophy, NeonatalMedium-chain Acyl-CoA Dehydrogenase DeficiencyVery Long Chain Acyl Coa Dehydrogenase DeficiencyMaple Syrup Urine Disease, Type 1BUsher Syndrome Type 1D/F Digenic (Diagnosis)Stickler Syndrome Type 2Stickler Syndrome Type 1Alport Syndrome, X-LinkedThyroid Dyshormonogenesis 6G6PD DeficiencyGlycogen Storage Disease IIGalactosemiasAgat DeficiencyLong-chain 3-hydroxyacyl-CoA Dehydrogenase DeficiencyBeta-Thalassemia3-Hydroxy-3-Methylglutaric AciduriaHermansky-Pudlak Syndrome 1Mucopolysaccharidosis Type 1Severe Combined Immunodeficiency, X LinkedDiabetes Mellitus, Permanent Neonatal3-Methylcrotonyl CoA Carboxylase 1 DeficiencyMethylmalonic Aciduria cblB TypeMethylmalonic Aciduria Due to Methylmalonyl-CoA Mutase DeficiencyMethylcobalamin Deficiency Type cblEUsher Syndrome, Type 1BPhenylketonuriasPancreatic Agenesis 1Glycogen Storage Disease IXCMOWSPseudohypoaldosteronism, Type IDIAR1Congenital Lipoid Adrenal Hyperplasia Due to STAR DeficiencyCongenital Isolated Thyroid Stimulating Hormone DeficiencyMenkes Disease17 Alpha-Hydroxylase DeficiencyMucopolysaccharidosis Type 7Ornithine Aminotransferase DeficiencyOrnithine Translocase DeficiencyPrader-Willi SyndromeFactor VII DeficiencyDiabetes MellitusHypophosphatasiaHomocystinuriaCombined Immunodeficiency Due to ZAP70 DeficiencyCarnitine-acylcarnitine Translocase DeficiencyGlucose Transporter Type 1 Deficiency SyndromePitt Hopkins SyndromeTuberous Sclerosis 1Ataxia With Isolated Vitamin E DeficiencyPermanent Neonatal Diabetes MellitusGlycogen Storage Disease Type IXA1Glutathione Synthetase DeficiencyNiemann-Pick Disease Type C2Mucopolysaccharidosis Type 3 ATuberous Sclerosis 2Krabbe DiseaseGlycogen Storage Disease ICGlycogen Storage Disease Type IBPropionic AcidemiaCongenital HypothyroidismHolocarboxylase Synthetase DeficiencyPtsdMetachromatic LeukodystrophySCDCystic FibrosisSickle Cell DiseaseSpinal Muscular AtrophyCystinosisHereditary Fructose Intolerance
NCT03655223RTI International30,000
Unknown
不适用
The Newborn Early Warning SystemDevelopment Tool NEWS
NCT05234151PXL University College1
招募中
不适用
Determining peak inspiratory flow during regular breathing in both healthy and lung sick patientsNormal lung physiologyRespiratory - Other respiratory disorders / diseasesRespiratory - Normal development and function of the respiratory systemBronchiolitis
ACTRN12608000215325Fisher and Paykel Healthcare60
The Effects of Auditory Interventions on Comfort and... | 临床试验