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Feeding and Sucking in Preterm Infants

B

Bozok University

Status

Completed

Conditions

Breast Feeding
Preterm Birth Complication

Treatments

Behavioral: oral motor stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT04751903
216S081 (Other Grant/Funding Number)

Details and patient eligibility

About

This study aimed to determine the effect of oral motor stimulation (OMS) in preterm infants for successful feeding and sucking.

Full description

In recent years, with advances in methods of neonatal resuscitation and caring methods, the survival rate of preterm infants has gradually increased. Sucking, swallow and respiratory dysfunction are widespread complications in the preterm infants that reason oral feeding difficulties. Safe and successful oral feeding requires proper maturation of sucking, swallowing, and respiration. The development of behaviors necessary for safe and successful nutrition begins long before birth. Jaw movements begin to be seen in the intrauterine 11th week. But sucking-swallowing-respiratory coordination is not sufficiently developed before 34 weeks of gestation. For this reason, preterm babies at the greater gestational week usually show more developed and consistent feeding skills. Maternal breast milk is best for neurodevelopment in preterm infants. Achieve oral feeding and maternal breast milk as early as possible is beneficial for preterm infants.

Oral motor stimulation (OMS) is defined as the sensorial stimulation of cheek, lip, jaw, upper-lower gum, internal cheek, tongue and soft palate that affects the physiology of oropharyngeal mechanisms and develops feeding functions. OMS used as an alternative or supplementary early intervention strategy to develop oral feeding skills in preterm infants. Previous studies have indicated that the use of OMS during or before the transition to oral feeding may not only have positive effects on the preterm infants' feeding behaviors but also enhance their general clinical course. Preterm infants who suffer from oral feeding problems often experience longterm health problems and delayed discharge from the hospital. A more effective feeding decreases adverse outcomes by decreasing hospital stays.

Preterm infants are required to prolonged NICU stay in order to stabilized, feeding, and gain optimal weight. Increasing prematurity and reduced birth weight lead to extensive resource utilization. In addition all nutritional options except breast milk increase the cost. OMS can develop sucking success and provide early oral feeding. Thus nurse labor and hospital costs may decrease and OMS can be a cost-effective application.

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Enrollment

77 patients

Sex

All

Ages

29 to 33 weeks old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Born between 29th and 34th gestational weeks, based on the mother's last menstruation date,
  • Percentile measurements consistent with their gestational week measurements,
  • Stable vital signs,
  • APGAR scores between 4 and 10 in the 1st and 5th minutes,
  • Stable for 48 hours after having received mechanical ventilation and/or continuous positive airway pressure,
  • Being breastfed,
  • Mother's eagerness to breastfeed the infant,
  • Voluntary participation of parents in the study.

Exclusion criteria

  • Suffered from severe asphyxia,
  • Born with a low birth weight according to gestational week,
  • Have intraventricular bleeding,
  • With a congenital anomaly,
  • Babies without their mother.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

77 participants in 2 patient groups

Oral motor stimulation
Experimental group
Description:
After the infants were assessed by a neonatologist, Oral motor stimulation was administered to the experimental group thrice a day (at 9:00, 12:00, 15:00 hours) for 15 minutes right before feeding, over a 14-day period.
Treatment:
Behavioral: oral motor stimulation
Control group
No Intervention group
Description:
The preterm infant' the control group were only fed by the researcher thrice a day (at 9:00, 12:00, 15:00 hours) over a 14-day period.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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