ClinicalTrials.gg
CompletedNCT05310851Updated May 29, 2024

The Effect Of Oral Motor Stimulation And Nonnutritive Sucking To The Time Of Transition To Oral Nutrition In Preterm

An interventional study of PIOMI and non-nutritive sucking in Preterm, Nutrition Disorder, Infant and Feeding; Difficult, Newborn, sponsored by Eskisehir Osmangazi University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 2 Days to 5 Days. Per ClinicalTrials.gov, last updated 2024-05-29.

Sponsored by Eskisehir Osmangazi University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 1 year 2 months after the study started (first participant enrolled Jan 2021, registered Mar 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
39
Allocation
Randomized
Ages
2 Days to 5 Days
Sex
All
01

Study summary

Oral feeding difficulty is one of the problems that preterm infants frequently experience due to poorly developed oral musculature. Sucking and swallowing are present in early fetal life, but sucking-swallowing and swallowing-respiratory coordination are respectively occurs after the 32 and 33-34 gestational week (GA). For this reason, although there are sucking movements in preterm babies with gestational weeks of 31 and below, oral feeding is difficult because adequate coordination cannot be achieved during sucking-swallowing and breathing. Until these structures develop, preterm babies are fed by gavage (nasogastric/orogastric route) in intensive care units. Gavage feeding causes many negativities such as preventing the advantages of oral nutrition and creating an entry route for infectious agents, and the discharge is also delayed. Thus, infants are exposed to adverse intensive care conditions for a longer period of time. For this reason, it is important to ensure the transition to full oral nutrition as soon as possible.

There are various methods that facilitate the transition of infants to oral feeding. Pacifier and oral stimulation applications are some of them. Oral stimulation was first applied by Fucile et al (2002). It is a method consisting of a total of 15 minutes, in which therapeutic touches are made for 12 minutes before feeding, and in the last few minutes, non-nutritive sucking is applied. Later, Lessen thought that this intervention was longer than the fragile preterm babies with a small oral cavity and shortened the duration of the intervention and reformatted it. This intervention, called "Premature Infant Oral Motor Intervention (PIOMI)" (Preterm Infant Oral Motor Intervention), is a 5-minute application consisting of 3 minutes of massage and 2 minutes of non-nutritive sucking. In the literature review, a study comparing oral motor stimulation and pacifier method was reached. However, in this study, unlike our study, a pacifier was applied to one of the groups, a 12-minute stimulation to the second, and a 12-minute stimulation and pacifier to the third. In our study, there are 3 groups. one of the groups a pacifier will be applied to one group and a 5-minute oral stimulation program will be applied to the other group. The third group is the control group.

The aim of the study is to evaluate the effect of pacifier and oral stimulation applied to preterm infants on the transition time to oral feeding.

Read the detailed description

The infant hospitalized in the intensive care unit will be evaluated primarily in terms of inclusion criteria in the sample group. The baby meeting the criteria will be evaluated by the neonatologist physician and, if appropriate, interviewed with the parents. Parents will be informed about the study and their written consent will be obtained. The group that the baby will be included in will be determined by the randomization method.

"Preterm Baby Information Form" created by the researcher will fill to all infants in the before the intervention. Then, body weight, height and head circumference will be measured and recorded in order to fill in the 1st day anthropometric measurements information in the Preterm baby follow-up form. Then, "Early Nutrition Skills Assessment Tool (EFS-Turkish)" will be applied to evaluate pre-intervention nutrition skills. Then, intervention will be started. Infants in the PIOMI group will receive a 5-minute PIOMI 30 minutes before feeding time. Infants in the non-nutritive sucking group will receive pacifier 3 minutes before 1 hour any feeding time and, 2 minutes before 10 minutes. PIOMI and non-nutritive sucking will be applied once daily for 14 days. only feeding follow-up will be done in the infants in the control group.

"Early Feeding Skills Assessment Tool (EFS-Turkish)" will be re-administered to all babies at the end of the fourteenth day. Nutritional follow-up will be done until the babies are discharged.

In nutritional follow-up will be evaluated time to transition to full oral feeding and how many cc it takes per minute.

02

Conditions studied

  • Preterm
  • Nutrition Disorder, Infant
  • Feeding; Difficult, Newborn

Keywords

  • preterm
  • oral motor stimulation
  • non-nutritive sucking
  • oral nutrition
03

In context

Premature Birth

2,610 studies on the registry are indexed under Premature Birth; 507 are open to participants now.

This study's enrollment of 39 is below the median of 84 across 1,722 interventional studies indexed under Premature Birth.

Browse Premature Birth studies →

Lead sponsor

Eskisehir Osmangazi University is the lead sponsor of 153 studies on the registry; 27 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
2 Days to 5 Days
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • gestational age of 29-34 weeks
  • Vital signs in balance for at least 24 hours,
  • 1st and 5th minute APGAR score of 4 and above,
  • postnatal 2-5 days
  • Babies with written and verbal consent from their parents

Exclusion criteria

Exclusion Criteria:

  • Congenital anomaly
  • Necrotizing enterocolitis
  • Intraventricular Bleeding
  • Babies receiving respiratory support other than high-flow nasal cannula
  • Babies who developed any complications during the follow-up period after being included in the study group and whose balance status deteriorated
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
39 participants (actual)

Study arms

  • Experimental
    PIOMI group

    Infants in the PIOMI group will receive a 5-minute PIOMI 30 minutes before feeding time. PIOMI will be applied once daily for 14 days.

    Other: PIOMI and non-nutritive sucking

  • Experimental
    Non-nutritive sucking group

    Infants in the non-nutritive sucking group will receive pacifier 3 minutes before 1 hour any feeding time and, 2 minutes before 10 minutes. Non-nutritive sucking will be applied once daily for 14 days.

    Other: PIOMI and non-nutritive sucking

  • No intervention
    control group

    only feeding follow-up will be done in the infants in the control group.

Interventions

  • OtherPIOMI and non-nutritive sucking

    PIOMI group; The first three minutes of the five minutes include massages aimed at strengthening the cheeks, lips, gums and tongue; the last two minutes consist of non-feeding suction application. Infants in the Non-nutritive sucking group will receive pacifier 3 minutes before 1 hour any feeding time and, 2 minutes before 10 minutes.

06

What researchers measure

Primary outcomes

  1. Early Nutrition Skills Assessment Tool (The Early Feeding Skills (EFS) Assessment-Turkish)

    It will be used to assess infants' oral feeding skills and readiness during the transition to oral feeding. Infants will be evaluated on the 1st and 14th days using this scale.A low score indicates that she has no nutritional skills, while a high score indicates that she has nutritional skills.

    Time frame: first day

  2. Early Nutrition Skills Assessment Tool (The Early Feeding Skills (EFS) Assessment-Turkish)

    It will be used to assess infants' oral feeding skills and readiness during the transition to oral feeding. Infants will be evaluated on the 1st and 14th days using this scale.A low score indicates that she has no nutritional skills, while a high score indicates that she has nutritional skills.

    Time frame: 14th day

  3. Nutritional follow-up

    Nutritional follow-up will be carried out from the day of starting the study until discharge. Feeding at 12am and 12pm will be taken into account in the nutrition follow-up. At these feeding times; \- How many cc it oral takes per minute will be recorded.

    Time frame: average of 1 month

  4. Nutritional follow-up

    Feeding babies with only a bottle or breast 8 times in 48 hours indicates that they are on full oral feeding. Dates when infants transition to full oral feeding will be recorded.

    Time frame: average of 1 month

Secondary outcomes

  1. rate of body weight gain

    birth weight and weight on the day of started study will be note.

    Time frame: first day

  2. rate of body weight gain

    Weight on the 7th day will be note.

    Time frame: 7th day

  3. rate of body weight gain

    Weight on the 14th day will be note.

    Time frame: 14th day

  4. rate of body weight gain

    weight on the day of discharge will be note.

    Time frame: one day

  5. discharge time

    The date of infants admission to the intensive care unit and the date of her discharge will be noted.

    Time frame: average of 1 month

07

Study locations

1 site
  • Eskisehir Osmangazi University
    Eskişehir, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 29, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05310851
Responsible party
Merve Çakırlı (Principal Investigator, Eskisehir Osmangazi University) — Principal investigator
First posted
Apr 5, 2022
Start date
Jan 10, 2021
Primary completion
Apr 10, 2023
Completion
Apr 10, 2023
Last update
May 29, 2024

Study contacts

Merve Cakirli
principal investigator · Eskisehir Osmangazi University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion