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Effect of Breast Milk Olfactory Stimulation (BMOS)

A

Ain Shams University

Status

Not yet enrolling

Conditions

Preterm Infant Feeding Outcomes

Treatments

Other: BMOS technique

Study type

Interventional

Funder types

Other

Identifiers

NCT06771882
olfactory stimulation

Details and patient eligibility

About

Breast milk olfactory stimulation will improve preterm infants' outcomes.

Full description

The researcher will explain the aim of the study and the components of the tools to the studied nurses.

  • The researcher will distribute questionnaire to studied nurses for assessing their knowledge and the researcher will observe their practices regarding breast milk olfactory stimulation for premature infants.
  • The researcher will be divided preterm infant randomly into two equal groups (control and study). While intervention will be directed to study group only before feeding. Both groups will be subjected to same routine care of the NICU.
  • The researcher will be used PIBB scale and neonatal behavioral responses Sheet to assess the premature infants at 1st day of admission as pre intervention after routine care as "change diaper, eye care, cord care, feeding" at morning shift at ten o'clock and one o'clock in the afternoon for study and control group (pre intervention).
  • The researcher will apply breast milk olfactory stimulation technique for study group only before feeding but, both groups will be subjected to same routine care of the NICU.
  • The researcher will assess the effect of used olfactory stimulation technique to study group at 5th and 6th day of admission post intervention.

Enrollment

52 estimated patients

Sex

All

Ages

30 to 30 weeks old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Preterm infant has gestational of 30 >37.
  • Birth weight 1000 > 2500 gm.
  • Preterm infant fed oral or gavage feeding or both of them.

Exclusion criteria

  • Preterm infants on mechanical ventilation or complicated case

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

52 participants in 1 patient group

BMOS technique
Active Comparator group
Description:
The researcher obtained 5cc soaked in a 2cm×2 cm piece of sterilized gauze for every intervention administration. * The preterm neonates were positioned in the supine position and the head turned to one side * The gauze was placed near the head, 2cm away from the nose for 2 minutes before feeding to stimulate an olfactory sense of preterm neonates 3 times per day (11 am, 2 pm, and 5 pm).
Treatment:
Other: BMOS technique

Trial contacts and locations

1

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Central trial contact

wafaa E ouda, Professor of Pediatric Nursing; Eman T Sayed, master

Data sourced from clinicaltrials.gov

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