Effect of Three Different Post-Feeding Positions on Vital Signs and Comfort Levels in Preterm Infants

June 22, 2024 updated by: Canan Ayaslı Ünal, Saglik Bilimleri Universitesi

The Effects of Post-Feeding Right Lateral, Supine, and Prone Positions on Heart Rate, Oxygen Saturation, Respiratory Rate, Pain Levels, and Comfort Levels in Preterm Infants

This study purpose to evaluate the effects of sequentially applying right lateral, supine, and prone positions after feeding on the vital signs and comfort levels of preterm infants between 28 and 36 weeks of gestation."

Study Overview

Detailed Description

Improvement in physiological parameters of preterm infants, facilitating and supporting cognitive and neuromotor development, and reducing pain and stress are recommended within the scope of developmental care through the application of therapeutic positions (supine, prone, and lateral positioning). There are discussions among neonatal nurses regarding the therapeutic positions applied to preterm infants after feeding.

This study is an experimental research designed as a single-group trial in which preterm infants meeting the inclusion criteria are subjected to sequentially applied right lateral, supine, and prone positions after feeding.The study included preterm infants between postnatal weeks 28 and 36, fed via orogastric tube, and receiving at least 75% of their energy intake enterally, with stable vital signs. Data collection utilized the Preterm Infant Demographic Information Form, Preterm Infant Vital Signs Observation and Monitoring Form, Neonatal Comfort Behavior Scale (ComfortNeo), and Neonatal Pain/Agitation Sedation Scale (N-PASS). According to the N-PASS, as the score increases, the pain level rises, with scale scores ranging from a minimum of 0 to a maximum of 10 point. According to the ComfortNeo Scale, as the comfort score increases, the baby's comfort level decreases, with scale scores ranging from a minimum of 6 to a maximum of 30.

In this study, preterm infants included in the sample group are fed via an orogastric tube in a semi-elevated supine position during their routine feeding time and then placed in the right lateral position. The infants' heart rate, oxygen saturation, respiratory rate, pain score, and comfort level data are evaluated and recorded immediately after feeding, one hour after feeding, and three hours after feeding while in the right lateral position. During the next routine feeding time, the infants are fed in the supine position and kept in this position, with their heart rate, oxygen saturation, respiratory rate, pain score, and comfort level data evaluated and recorded immediately after feeding, one hour after feeding, and three hours after feeding. During the subsequent routine feeding time, the infants are fed in the supine position and then placed in the prone position. The same parameters are evaluated and recorded immediately after feeding, one hour after feeding, and three hours after feeding while in the prone position. This procedure is repeated for each infant for three days to ensure data accuracy. The positions applied to the infants are standardized and applied in the same order to prevent variability in the data.

Study Type

Interventional

Enrollment (Actual)

48

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Ankara, Turkey, 06010
        • Health Science University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Postnatal weeks 28-36 of gestation
  • Weighing over 1000 grams at the time of the study
  • Hospitalized for at least two days
  • Fed via orogastric tube
  • With enteral feeding accounting for at least 75% of energy intake
  • Stable vital signs and spontaneous respiration

Exclusion Criteria:

  • Mechanically ventilated due to respiratory distress
  • Receiving analgesic or sedative medications
  • Undergoing treatment with inotropic drugs
  • Diagnosed with congenital anomalies
  • Undergoing medical or surgical treatment for patent ductus arteriosus
  • Requiring drainage or chest tube insertion for pneumothorax
  • Diagnosed with necrotizing enterocolitis
  • Receiving medical treatment for gastroesophageal reflux or diagnosed with cleft palate-lip anomalies

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: N/A
  • Interventional Model: Sequential Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Right lateral, supine, and prone position
In this study, the right lateral, supine, and prone positions were applied to each infant sequentially, consecutively, under identical conditions, and within the same time frame. Each position was maintained for three hours immediately after each infant's routine feeding time. Each position was applied immediately after feeding. Data on heart rate, oxygen saturation, respiratory rate, pain level, and comfort level were recorded immediately after positioning, one hour later, and three hours later. This procedure was repeated in the same manner, sequence, and time frame for three consecutive days.
Each infant included in the sample group is fed at their routine feeding time (9:00 a.m.), followed by placement in the right lateral position. Immediately after this position is applied, as well as one hour and three hours later, data on heart rate, oxygen saturation, respiratory rate, pain level, and comfort level are recorded. This procedure is repeated after the subsequent feeding time (12:00 p.m.) for the supine position and after the feeding time following that (6:00 p.m.) for the prone position. This procedure is repeated for three consecutive days at the same feeding times and in the same sequence.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The effect of the right lateral position on heart rate
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of post-feeding application of the right lateral position on heart rate (beats per minute: 100-180/min) in preterm infants
immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the right lateral position on oxygen saturation
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of post-feeding application of the right lateral position on oxygen saturation (peripheral oxgyen saturation / SpO2: %95-%100) in preterm infants
immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the right lateral position on respiratory rate
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of post-feeding application of the right lateral position on respiratory rate (respiratory per minute: 40-60/min) in preterm infants
immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the right lateral position on pain level
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of post-feeding application of the right lateral position on pain level (Evaluted according to the N-PASS:Neonatal Pain Agitation And Sedation Scale / min point: 0 max point: 10) in preterm infants. Pain level increases as the score rises.
immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the right lateral position on comfort level
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the right lateral position applied to preterm infants on the comfort level according to the ''Newborn Comfort Behavior Scale (ComfortNeo)" (min point:6 - max point: 30). As the comfort score increases, the level of comfort decreases.
immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the supine position on heart rate
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of post-feeding application of the supine position on heart rate (beats per minute) in preterm infants
immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the supine position on oxygen saturation
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of post-feeding application of the supine position on oxygen saturation (peripheral oxgyen saturation / SpO2) in preterm infants
immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the supine position on respiratory rate
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of post-feeding application of the supine position on respiratory rate (respiratory per minute) in preterm infants
immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the supine position on pain level
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of post-feeding application of the supine position on pain level (Evaluted according to the N-PASS:Neonatal Pain Agitation And Sedation Scale / min point: 0 max point: 10) in preterm infants. Pain level increases as the score rises.
immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the supine position on comfort level
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the supine position applied to preterm infants on the comfort level according to the ''Newborn Comfort Behavior Scale (ComfortNeo)"(min point:6- max point: 30). As the comfort score increases, the level of comfort decreases.
immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the prone position on heart rate
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of post-feeding application of the prone position on heart rate (beats per minute) in preterm infants
immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the prone position on respiratory rate
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of post-feeding application of the prone position on respiratory rate (respiratory per minute) in preterm infants
immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the prone position on pain level
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of post-feeding application of the prone position on pain level (Evaluted according to the N-PASS:Neonatal Pain Agitation And Sedation Scale / min point: 0 max point: 10) in preterm infants. Pain level increases as the score rises.
immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the prone position on comfort level
Time Frame: immediately after the post-feeding, first hour post-feeding, third hour post-feeding
The effect of the prone position applied to preterm infants on the comfort level according to the ''Newborn Comfort Behavior Scale (ComfortNeo) " (min point:6- max point: 30). As the comfort score increases, the level of comfort decreases.
immediately after the post-feeding, first hour post-feeding, third hour post-feeding

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: CANAN AYASLİ UNAL, Health Science University
  • Principal Investigator: Dilek YILDIZ, Prof., Health Science University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2022

Primary Completion (Actual)

September 20, 2022

Study Completion (Actual)

September 30, 2022

Study Registration Dates

First Submitted

June 8, 2024

First Submitted That Met QC Criteria

June 22, 2024

First Posted (Actual)

June 25, 2024

Study Record Updates

Last Update Posted (Actual)

June 25, 2024

Last Update Submitted That Met QC Criteria

June 22, 2024

Last Verified

June 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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