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NCT Number: NCT05077345

The Effects of Different Procedures on Pain Levels at Preterm and Term Infants in Neonatal Intensive Care Unit

Accurate assessment of pain in neonates in the neonatal intensive care unit (NICU) is vital because of the high prevalence of painful experiences, including both daily procedural pain and postoperative pain, in this population. It has been reported that newborns born between the gestational ages (GY) 25-42 and hospitalized in the NICU undergo an average of 14 painful procedures per day in the first 2 weeks of life. The aim of this study is determinin the effect of different procedures on the pain levels of newborns in the Neonatal Intensive Care Unit (NICU).

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Key information

About this study

Accurate assessment of pain in neonates in the neonatal intensive care unit (NICU) is vital because of the high prevalence of painful experiences, including both daily procedural pain and postoperative pain, in this population. Exposure of these infants to many mandatory invasive procedures and poor pain management during this time may lead to different results in the short and long term. Every painful application in newborns causes behavioral and physiological instability. Repeated exposure to painful stimuli produces long-term changes in stress-sensitive brain systems such as the hypothalamic-adrenal system and the developing brain. Therefore, evaluation and prevention of pain in newborns is essential. In the NICU, many medical interventions are often performed on infants that are repetitive, painful, but diagnostically necessary. All environmental stress factors can cause physiological changes such as increased pulse, blood pressure, respiratory rate and a decrease in oxygen saturation in newborns. Increasing energy expenditure to overcome these changes may affect physiological functioning, slowing recovery and adversely affecting the organization of the central nervous system (CNS). Heel blood (TC), vascular access (DY), naso and orogastric (NG-OG) catheter insertion, arterial blood collection, tracheal intubation (TE), various rectal procedures, removal of adhesive tapes, umbilical catheter (UK) insertion and removal, Various procedures such as aspiration, chest physiotherapy applications, diaper changing, various hand contacts, and general body care may induce pain responses in newborns. While these responses are associated with low cognitive and motor scores in early childhood, they may result in changes in visual-perceptual ability and somatosensory sensitivity later on. There are many studies in the literature to increase and prove the accuracy of pain assessment tools. However, since the pain treatments used in these studies were also varied, the homogeneity of the evaluations was insufficient. Therefore, more systematic evaluation studies should be conducted on how to improve pain management in NICUs. Finding which of the painful stimuli affects infants more will also guide the use of treatment methods. The aim of this study is to investigate the effects of different procedures applied in the NICU on the pain levels of term and preterm infants.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Preterm and term infants admitted to the NICU for the first time for various reasons with a hospital stay ranging from 1 to 8 days
  • Preterm and term infants who were cared for in an incubator without any pharmacological or non-pharmacological analgesic therapy, muscle relaxant, and sedation treatment in the last 24 hours before the procedure.

Exclusion criteria

  • Exposed to painful procedures more than 3 times in the same day
  • Infants who diagnosed with osteomyelitis, sepsis, pyejonic arthritis, congenital anomaly (Spina bifida, arthrogryposis multiplex congenita)
  • Infants with any known neurological diagnosis (Abnormal MRI finding, hydrocephalus, Chiari malformation, asphyxia, periventricular leukomolacia (PVL), acute bilirubin encephalopathy, hypoxic ischemic encephalopathy (HIE))
  • Infants who had any surgery

Treatment and study plan

Primary outcomes

  1. Neonatal Infant Pain Scale

    Time frame: The pain scale was scored in the first 5 minutes following the clinical procedure.

    pain measurement of infants. This scale measures five behavioral groupings (i.e. facial expressions, crying, movements of arms and legs, and awake condition), and one physiological parameter (i.e. breathing patterns) given against pain during invasive procedures in preterm and term infants. The total score is between "0" and "7". The lowest pain level is 0, and the highest pain level is 7. The validity and reliability of the scale were shown in studies that were conducted with premature and term newborns.

  2. O₂ saturation1

    Time frame: O₂ saturation value of the newborn 5 minutes before the painful procedure from the pulse oximeter.

    O₂ saturation of the newborn 5 minutes before the painful procedure.

  3. heart rate1

    Time frame: the heart rate of the newborn 5 minutes before the painful procedure from the monitor

    the heart rate of the newborn 5 minutes before the painful procedure

  4. heart rate2

    Time frame: the heart rate of the newborn at the time point of the painful procedure from the monitor

    the heart rate of the newborn during the painful procedure

  5. heart rate3

    Time frame: the heart rate of the newborn 5 minutes after the painful procedure from the monitor

    the heart rate of the newborn 5 minutes after the painful procedure

  6. O₂ saturation2

    Time frame: O₂ saturation of the newborn at the time point of the painful procedure from the pulse oximeter.

    O₂ saturation of the newborn during the painful procedure.

  7. O₂ saturation3

    Time frame: O₂ saturation of the newborn 5 minutes after the painful procedure from the pulse oximeter.

    O₂ saturation of the newborn 5 minutes after the painful procedure.

Secondary outcomes

  1. The type and Number of painful procedures

    Time frame: The type and number of painful procedures during the first 8 days of life performed on newborns were also recorded.

    The type and number of painful procedures will be recorded as Heel Puncture (HP), Venous Blood sampling (VB), naso and orogastric (NG-OG) catheter insertion, arterial blood collection, Tracheal Intubation (TI), several rectal procedures, the removal of adhesive tapes, insertion and removal of Umbilical Catheter (UC), and several other procedures such as aspiration, chest physiotherapy procedures,

  2. age (day)

    Time frame: up to 7 days

    age of the infants will be recorded as day.

  3. length (centimeter/cm)

    Time frame: It will be recorded on the pain assesment day.

    birth length of the infants

  4. gender

    Time frame: up to 7 days

    gender of the infants will be recorde as f/m

  5. Diagnosis of the infants (the reason for hospitalization of the infants)

    Time frame: up to 7 days

    the reason for hospitalization of the infants will be recorded as Prematurity, Respiratuar Distress Syndrome (RDS), Bronchopulmonary Dysplasia (BPD), Low birth weight (LBW), Extreme low birth weight (ELBW), Sepsis, Patent Ductus Arteriosus (PDA), Retinopathy of Prematurity (ROP), Small for gestational age (SGA), Premature Rupture of Membranes (PROM).

  6. the duration (day) of hospitalization of infants

    Time frame: up to 7 days

    the duration of hospitalization of all infants will be recorded as day.

  7. birth weight

    Time frame: at birth

    birth weight will be recorded in kilograms(kg)

Sponsors and collaborators

Lead sponsor

Sanko University

Other

Collaborators

  • Kahramanmaras Sutcu Imam University

Registry information

Acronym: PAIN

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Oct 14, 2021
Registry last updated
Apr 7, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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