The Effect of Position on Gastric Residual Volume and Comfort Level in Newborns

Comfort Clinical Trial

Official title:

The Effect of Position in Post-op Newborns Hospitalized in Pediatric Cardio Vascular Surgery Intensive Care Unit on Gastric Residual Volume and Comfort Level

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04596202
• Other study ID #: CanakkaleOMU
• Status: Completed
• Phase: N/A
• Start date: December 1, 2021
• Est. completion date: February 7, 2023

Study information

• Verified date: February 2023
• Source: Çanakkale Onsekiz Mart University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this randomized controlled trial is to determine the effect of different positions (supine, prone, right lateral and left lateral) in post-op term newborns staying in Pediatric Cardio Vascular Surgery (PCVS) Intensive Care Unit on gastric residual volume and comfort level.

Description:

In the study, crossover design from experimental designs was preferred. Crossover design is an experimental design type in which two or more interventions are applied in a sequence to each case in the study group. In these studies, each group is its own control group. In this design type, all different interventions in the study are applied to the same case; thus, differences that may arise due to individual differences are prevented. Additionally, less number of cases is sufficient in order to obtain the same number of observation data compared to the other design examples. Due to these properties, randomized crossover design model was used in this study. The study will be conducted in PCVS Intensive Care Unit of a University Hospital in Turkey between October 2020 and August 2021. In this study, sample size was calculated at the confidence interval of 95% using "G. Power-3.1.9.4" program. In a study the effect size used for determining the sample size in the study was found to be 0.54 based on the mean and standard deviation values of the study. By using this effect size, minimum sample size was found as 38 children in order for the gastric residue amount difference between positions to express statistically significance (p<0.05) with theoretical power of 0.95. By considering that there might be losses in the study, it is planned to include a total of 44 children in the study. The order of the 4 positions to be given to the infants in the study group (A:Prone Position, B:Right lateral Position, C:Left lateral Position, D:Supine Position) was determined by lot method. 4 different orders were chosen randomly from all possible orders of 4 positions to be given to the infants in the study group (24 different orders). Each different order of the positions was expressed as a group. 4 orders randomly selected from 24 different orders were as follows: The order in the first group is A, C, D, and B; The order in the second group is D, A, B, and C; The order in the third group is C, B, A, and D; The order in the fourth group is B, D, C, and A. Groups and position orders according to the result of the draw: 1. st GROUP ORDER; Prone (A), Left lateral (C), Supine (D), and Right lateral (B) 2. nd GROUP ORDER; Supine (D), Prone (A), Right lateral (B), and Left lateral (C) 3. rd GROUP ORDER; Left lateral (C), Right lateral (B), Prone (A), and Supine (D) 4. th GROUP ORDER; Right lateral (B), Supine (D), Left lateral (C), and Prone (A) Assigning the infants to 4 groups was made in Microsoft Excel program using "RANDBETWEEN" command. All positions will be applied once to each infant. The newborns to be assigned to the groups according to this result are stated in the below table. Groups Newborns 1. st group A, C, D, B 1, 5, 10, 11, 12, 20, 21, 30, 36, 38, 44 2. nd group D, A, B, C 19, 22, 23, 24, 25, 27, 28, 31, 32, 33, 42 3. rd group C, B, A, D 3, 4, 6, 7, 9, 13, 15, 29, 34, 37, 43 4. th group B, D, C, A 2, 8, 14, 16, 17, 18, 26, 35, 39, 40, 41 Data Collection tools: In the data collection, "Information Form" prepared by the researcher to record the descriptive information of the newborn, "Newborn Comfort Behavior Scale" to evaluate the comfort level and "Residue Follow-up Form" to record the residual amount and the "Vital Signs Follow-up Form" to record the vital signs will be used. Information Form: It is a form prepared by the researcher in line with the literature to record the natal and postnatal information of the newborn. The information in this form will be filled out by the researcher. Newborn Comfort Behavior Scale: It is a Likert-type scale developed to be used to assess sedation and comfort needs, pain, and distress of newborns followed-up in the intensive care. The Newborn Comfort Behavior Scale will be evaluated at the 30th, 60th and 120th minutes after the position. The comfort level scale scoring will be evaluated and filled by the researcher and a second observer working in the Intensive Care Unit for 5 years. Residue Follow-up Form: The form prepared to follow up the residue includes the position given, amount of nutrition, the way of feeding, feeding type, and residue amount control. The researcher will evaluate and fill out the form at the 30th, 60th and 120th minutes after feeding. Vital Signs Follow-up Form: This form prepared by the researcher in line with the literature was composed of the parameters of heart rate (min), respiratory rate (min) and oxygen saturation value (%SpO2) of the newborn. The researcher will evaluate and fill out the form at the 30th, 60th and 120th minutes after positioning.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44
• Est. completion date: February 7, 2023
• Est. primary completion date: January 1, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 1 Day to 30 Days

Eligibility

Inclusion Criteria:

• • Having a gestational week of 37 and above,
• Undergoing heart surgery,
• Being separated from the mechanical ventilator,
• Starting to be fed with nasogastric or orogastric tube,
• Not showing any signs of infection,
• Not using narcotic drugs in post-op period,
• Having no factors that can interfere with feeding (vomiting, distention, necrotizing enterocolitis, etc.)
• Having no condition that can prevent positioning,
• Receiving Informed Consent Form from their families.

Exclusion Criteria:

• • Having a gestational week of less than 36+6 days,
• Have not been separated from the mechanical ventilator,
• Showing any signs of infection,
• Using narcotic drugs in the post-op period,
• Having factors that may prevent feeding (vomiting, distention, necrotizing enterocolitis, etc.)
• Having a condition that can prevent positioning,
• Receiving no consent from their mother or father.

Related Conditions & MeSH terms

• Comfort
• Newborn, Infant, Disease
• Position
• Residual

Intervention

Behavioral:
• Supine position
After the infants are treated and fed, they will be given the supine position. After positioning, the residue control will be performed in accordance with the procedure steps guideline at the 30th, 60th and 120th minutes and it will be recorded on residue follow-up form. In addition, the comfort level, heart rate, respiratory rate, and oxygen saturation levels of the infant will be evaluated and recorded at the specified times. At the end of two hours, until the next feeding hour (between 121st-180th minutes), the routine position (supine position) applied in the clinic will be given to the infant and waited in order for physiological parameters and comfort levels to return the period without intervention. The aim here is to ensure for the case to get over the effect of the previous position. No data will be collected within this period.
• Prone position
After the infants are treated and fed, they will be given the prone position. After positioning, the residue control will be performed in accordance with the procedure steps guideline at the 30th, 60th and 120th minutes and it will be recorded on residue follow-up form. In addition, the comfort level, heart rate, respiratory rate, and oxygen saturation levels of the infant will be evaluated and recorded at the specified times. At the end of two hours, until the next feeding hour (between 121st-180th minutes), the routine position (supine position) applied in the clinic will be given to the infant and waited in order for physiological parameters and comfort levels to return the period without intervention. The aim here is to ensure for the case to get over the effect of the previous position. No data will be collected within this period.
• Lateral position
After the infants are treated and fed, they will be given the left or right position. After positioning, the residue control will be performed in accordance with the procedure steps guideline at the 30th, 60th and 120th minutes and it will be recorded on residue follow-up form. In addition, the comfort level, heart rate, respiratory rate, and oxygen saturation levels of the infant will be evaluated and recorded at the specified times. At the end of two hours, until the next feeding hour (between 121st-180th minutes), the routine position (supine position) applied in the clinic will be given to the infant and waited in order for physiological parameters and comfort levels to return the period without intervention. The aim here is to ensure for the case to get over the effect of the previous position. No data will be collected within this period. These processes will continue until the 4 positions are completed. Infants will stay in each position for 2 hours.

Locations

Country	Name	City	State
Turkey	Fatma Yilmaz Kurt	Çanakkale	Canakkale

Sponsors (1)

Lead Sponsor	Collaborator
Çanakkale Onsekiz Mart University

Country where clinical trial is conducted

Turkey, 

References & Publications (5)

Chen SS, Tzeng YL, Gau BS, Kuo PC, Chen JY. Effects of prone and supine positioning on gastric residuals in preterm infants: a time series with cross-over study. Int J Nurs Stud. 2013 Nov;50(11):1459-67. doi: 10.1016/j.ijnurstu.2013.02.009. Epub 2013 Mar — View Citation

Kaur V, Kaur R, Saini SS. Comparison of Three Nursing Positions for Reducing Gastric Residuals in Preterm Neonates: A Randomized Crossover Trial. Indian Pediatr. 2018 Jul 15;55(7):568-572. — View Citation

Khatony A, Abdi A, Karimi B, Aghaei A, Brojeni HS. The effects of position on gastric residual volume of premature infants in NICU. Ital J Pediatr. 2019 Jan 8;45(1):6. doi: 10.1186/s13052-018-0591-9. — View Citation

Ozdel D, Sari HY. Effects of the prone position and kangaroo care on gastric residual volume, vital signs and comfort in preterm infants. Jpn J Nurs Sci. 2020 Jan;17(1):e12287. doi: 10.1111/jjns.12287. Epub 2019 Oct 23. — View Citation

Yayan EH, Kucukoglu S, Dag YS, Karsavuran Boyraz N. Does the Post-Feeding Position Affect Gastric Residue in Preterm Infants? Breastfeed Med. 2018 Jul/Aug;13(6):438-443. doi: 10.1089/bfm.2018.0028. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Neonatal Comfort Behavior Scale (COMFORTneo):"change" will be assessed	This scale is a Likert type scale developed to be used in the evaluation of sedation and comfort needs, pain and distress of newborns followed-up in intensive care. COMFORTneo is composed of six parameters including alertness, calmness/agitation, respiratory response, crying, body movements, facial tension, and muscle tone. Each item in the scale is scored from 1 to 5. It is evaluated over the total score. The lowest score of COMFORTneo is 6 and the highest score is 30. If total score of the scale is between 9-13 points, it refers that the infant is "comfortable". If it is between 14-30 points, it is emphasized that the infant has "pain or distress", is uncomfortable and requires interventions that will provide comfort.	The Newborn Comfort Behavior Scale will be evaluated at the 30 to 120 minutes after the position.
Primary	Residue Follow-up Form: "change" will be assessed	The form prepared to follow up the residue includes the position given, amount of nutrition, the way of feeding, feeding type, and residue amount control.	It will be checked at 30 to 120 minutes after feeding.
Primary	Vital Signs Follow-up Form: "change" will be assessed	This form prepared by the researcher in line with the literature was composed of the parameters of heart rate (min), respiratory rate (min) and oxygen saturation value (%SpO2) of the newborn.	It will be evaluated at 30 to 120 minutes after positioning.
Secondary	Heart Rate (min): "change" will be assessed	The heart rate per minute will be obtained using a pulse oximeter device. A separate pulse oximeter probe will be placed on each of the infants.	It will be evaluated at 30 to 120 minutes after positioning.
Secondary	Oxygen Saturation (%SpO2): "change" will be assessed	Oxygen saturation (SpO2) will be obtained using a pulse oximeter device. A separate pulse oximeter probe will be placed on each of the infants. Pulse oximeter is a noninvasive, painless, and reliable method used to measure oxygen saturation (SpO2) in arterial blood. The rate of hemoglobin carrying oxygen in arterial blood is measured and the qualifying result is defined as functional oxygen saturation.	It will be evaluated at 30 to 120 minutes after positioning.
Secondary	Respiration Rate (min): "change" will be assessed	The respiration rate is the number of inspirations per minute. It is counted by chest movements or auscultation.	It will be evaluated at 30 to 120 minutes after positioning.