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Effects of Oral Stimulation and Supplemental Nursing System

M

Muğla Sıtkı Koçman University

Status

Completed

Conditions

Breastfeeding

Treatments

Device: Oral motor stimulation (OMS) and The supplemental nursing system (SNS)

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study aimed to investigate the effect of oral stimulation and a supplemental nursing system on the time to full maternal breastfeeding and sucking success in preterm infants.

Full description

This study aimed to investigate the effect of oral stimulation and a supplemental nursing system on the time to full maternal breastfeeding and sucking success in preterm infants. The sample consisted of 70 preterm babies. Oral motor stimulation and a supplemental nursing system were applied to the preterm infants in the experimental group, while no intervention was applied to those in the control group.

Enrollment

70 patients

Sex

All

Ages

1 to 30 days old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • a birth weight of 1,000 gr and above,
  • a gestational age between 30 and 34 weeks,
  • no congenital anomaly,
  • no severe asphyxia or chronic lung disease,
  • spontaneous breathing,
  • grades III and IV intracranial hemorrhage and no periventricular leukomalacia

exclusion criteria.

  • congenital anomaly
  • grades III and IV intracranial hemorrhage and periventricular leukomalacia

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

70 participants in 2 patient groups

Oral Stimulation and Supplemental Nursing System group
Experimental group
Description:
Oral motor Stimulation (OMS) and an Supplemental Nursing System (SNS) were applied to preterm infants in the experimental group.
Treatment:
Device: Oral motor stimulation (OMS) and The supplemental nursing system (SNS)
control group
No Intervention group
Description:
The clinic's routine feeding protocol was applied to the babies in the control group.

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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