A Comparison Study of Feeding Prematures in the Side-lying Position on the Right and Left Side - a Pilot Study.

NCT ID: NCT04987983

Last Updated: 2023-03-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 8 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-06-28
• Study Completion Date: 2021-09-23

Brief Summary

Methods and techniques to improve the quality and safety of oral feeding in preterm infants are still a significant challenge in modern neonatology. One of the areas that can help improve feeding is choosing the optimal feeding position for premature babies.

Detailed Description

PURPOSE: The aim of the study is to compare the advantages of side-lying positioning on the right (SLP-R) and left side (SLP-L) of infant's body, during bottle-feeding of preterm infants.

METHOD: The study will include eight neonates (n=8) born ≤34 weeks of gestational age. Four bottle-feeding sessions will be tested in each of the newborns: two in the SLP-R and two in the SLP-L. The position for the first study will be randomly assign, then positioning will be change after each feeding session. In one day, only two consecutive feeding sessions will be tested which will be included to the study in order to minimize fatigability as a disrupting factor. The levels of saturation (SpO2) and heart rate (HR) will be measured as the parameters indicative of the newborn's physiological stability. The factors determining the qualitative aspect of feeding include the total time of declines of SpO2 ≤85%, level of the newborn's alertness according to the Neonatal Behavioral Assessment Scale (NBAS), and the occurrence of choking episodes. The proportion of milk consumed (volume of milk eaten relative to the expected volume) and the duration of the feeding and feeding session were also will be record. Maximum time of feeding session will be 40 minutes.

Also the posseting during/after feeding and regurgitations will be record in each tested positions.

Conditions

Bottle Feeding; Premature

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Experimental SLP-R

Infant placed in a SLP-R on the researcher's lap. Infant body positioned on side-lying position on the right side of it's body. Head of the infant symmetrically placed between the shoulders, supported by the researcher's. Shoulder girdle higher than the pelvic girdle, head and back in a straight line - a slight natural bend of the body is allowed. Legs bent at an angle of approx. 90° in the natural flexion of the knee and ankle joint. The infant's arms close to the midline (on the bottle or researcher's hands)

Group Type: EXPERIMENTAL

Experimental SLP-R

Intervention Type: OTHER

SLP-R will be given to the infant during bottle-feeding.

Experimental SLP-L

Infant placed in a SLP-L on the researcher's lap. Infant body positioned on side-lying position on the left side of it's body. Head of the infant symmetrically placed between the shoulders, supported by the researcher's. Shoulder girdle higher than the pelvic girdle, head and back in a straight line - a slight natural bend of the body is allowed. Legs bent at an angle of approx. 90° in the natural flexion of the knee and ankle joint. The infant's arms close to the midline (on the bottle or researcher's hands).

Group Type: EXPERIMENTAL

Experimental SLP-L

Intervention Type: OTHER

SLP-L will be given to the infant during bottle-feeding.

Interventions

Experimental SLP-R

SLP-R will be given to the infant during bottle-feeding.

Intervention Type: OTHER

Experimental SLP-L

SLP-L will be given to the infant during bottle-feeding.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• circulatory and respiratory stability;
• readiness for oral feeding according to each child's Speech-Language Pathologist assessment;
• prematurely born infants who will be in the process of transfer from enteral nutrition to full oral feeding and will be fed orally at least 4 times within twenty-four hours;
• researcher must be a right handed person (right hand is the dominant hand);
• each infant will be fed with one kind of bottle and nipple;
• parents will give a informed consent to participate their infant in the study.

Exclusion Criteria

• disorders which could significantly affect the feeding course, such as cleft lip and/or palate, facial paralysis and/or congenital defects of the facial skeleton;
• the presence of detected congenital abnormalities and metabolic diseases;
• newborns after abdomen chirurgical treatment;
• low Apgar score (less than 5 points at the 5th and 10th minute of the measurement);
• administered analgesics, anticonvulsants and sedatives <72 hours from extubation prior the trial;
• parenterally fed infants;
• infants with administered intravenous infusion with glucose;
• parents refusal to participate in the study or when bottle-feeding will not be the parental preference.

• Minimum Eligible Age: 32 Weeks
• Maximum Eligible Age: 38 Weeks
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Polish Mother Memorial Hospital Research Institute

OTHER

Sponsor Role: lead

Responsible Party

Anna Raczyńska

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Anna D Raczyńska, PhD

Role: PRINCIPAL_INVESTIGATOR

Polish Mother's Memorial Hospital - Research Institute

Locations

Polish Mother's Memorial Hospital - Research Institute

Lodz, , Poland

Countries

Poland

Other Identifiers

PMMHRI-2021

Identifier Type: -

Identifier Source: org_study_id