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Comparison of the Effects of Oral Stimulation and Non-nutritive Sucking Practices

Primary Purpose

Premature, Nutrition Disorders, Sucking Behavior

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Pacifier
Oral stimulation
Sponsored by
Ankara City Hospital Bilkent
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Premature focused on measuring Sucking, Oral stimulation, Premature baby

Eligibility Criteria

undefined - 6 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Preterm babies born between 26-32 weeks (including 26 and 32 weeks)

Exclusion Criteria:

  • Babies with congenital anomalies
  • Babies born with asphyxia
  • Babies with major GIS anomalies
  • Babies who have undergone major GIS surgery

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Experimental

    Experimental

    Experimental

    No Intervention

    Arm Label

    Group 1 (Oral stimulation)

    Group 2 (Pacifier)

    Group 3 (oral stimulation + pacifier)

    Group 4 (Enteral feeding by tube)

    Arm Description

    The group that will receive oral stimulation with the Backman method once a day from the 29th week

    The group that will be given a pacifier three times a day from the 29th week

    Starting from the 29th week, the group will be given a pacifier three times a day and a Backman oral stimulation will be applied once a day.

    The group fed enterally by tube in routine practice, in which no intervention will be made.

    Outcomes

    Primary Outcome Measures

    Full oral feeding time (postmenstruel week)
    The effect of oral stimulation and/or pacifier use on full oral feeding time in premature infants.
    Hospital stay (days)
    The effect of oral stimulation and/or pacifier use on hospital stay in premature infants

    Secondary Outcome Measures

    Full Information

    First Posted
    December 11, 2021
    Last Updated
    February 18, 2022
    Sponsor
    Ankara City Hospital Bilkent
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05249179
    Brief Title
    Comparison of the Effects of Oral Stimulation and Non-nutritive Sucking Practices
    Official Title
    Comparison of the Effects of Oral Stimulation and Non-nutritive Sucking Practices on the Transition to Full Oral Feeding in Infants With a Gestational Age of 26-32 Weeks
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2021
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    April 1, 2022 (Anticipated)
    Primary Completion Date
    January 1, 2024 (Anticipated)
    Study Completion Date
    August 1, 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Ankara City Hospital Bilkent

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    This study, it was aimed to compare the effects of oral stimulation and non-nutritive sucking practices on the transition to full oral feeding in babies with a gestational age of 26-32 weeks. Non-oral feeding methods are frequently used in babies born prematurely since sucking and sucking-swallowing coordination have not yet developed. While some premature babies gain the sucking and swallowing reflexes faster, some of them cannot develop this reflex for a long time, so the length of hospital stay is prolonged. All infants who can be fed completely enterally (PMA >29 weeks) will be randomized into 4 groups as oral stimulation (group 1), pacifier (group 2), oral stimulation + pacifier (group 3), and control group by using a stratified blocked randomization method with a block size of 4. Stratification on GA (26-27, 28-29, 30-32 weeks GA) was used to ensure that the groups had similar gestational age distribution. The time of the patients to start breastfeeding and the length of hospital stay (days) will be compared.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Premature, Nutrition Disorders, Sucking Behavior
    Keywords
    Sucking, Oral stimulation, Premature baby

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    140 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Group 1 (Oral stimulation)
    Arm Type
    Experimental
    Arm Description
    The group that will receive oral stimulation with the Backman method once a day from the 29th week
    Arm Title
    Group 2 (Pacifier)
    Arm Type
    Experimental
    Arm Description
    The group that will be given a pacifier three times a day from the 29th week
    Arm Title
    Group 3 (oral stimulation + pacifier)
    Arm Type
    Experimental
    Arm Description
    Starting from the 29th week, the group will be given a pacifier three times a day and a Backman oral stimulation will be applied once a day.
    Arm Title
    Group 4 (Enteral feeding by tube)
    Arm Type
    No Intervention
    Arm Description
    The group fed enterally by tube in routine practice, in which no intervention will be made.
    Intervention Type
    Other
    Intervention Name(s)
    Pacifier
    Intervention Description
    Preterm infants in Groups 2 and 3 will suck a pacifier 3 times a day (09:00, 12:00, 15:00) for 3 minutes before feeding and then they will be fed with the O/G feeding tube.
    Intervention Type
    Other
    Intervention Name(s)
    Oral stimulation
    Intervention Description
    Infants in groups 1 and 3 will receive a prefeeding oral stimulation program once a day, 15 to 30 minutes before a tube feeding. Oral stimulation programs will be delivered by trained nurses or pediatric physical therapies. Nurses will be trained to deliver the stimulation program to the infants, by a member from the pediatric physical therapies medical staff, before the beginning of the study. Based on Backman's principles, the pre-feeding oral stimulation program consisted of a 12-minute stimulation program that included stroking the cheeks, lips, gums, and tongue.
    Primary Outcome Measure Information:
    Title
    Full oral feeding time (postmenstruel week)
    Description
    The effect of oral stimulation and/or pacifier use on full oral feeding time in premature infants.
    Time Frame
    2 years
    Title
    Hospital stay (days)
    Description
    The effect of oral stimulation and/or pacifier use on hospital stay in premature infants
    Time Frame
    2 years

    10. Eligibility

    Sex
    All
    Maximum Age & Unit of Time
    6 Months
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Preterm babies born between 26-32 weeks (including 26 and 32 weeks) Exclusion Criteria: Babies with congenital anomalies Babies born with asphyxia Babies with major GIS anomalies Babies who have undergone major GIS surgery
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Mustafa S Akin, Specialist
    Phone
    +90 555 876 05 85
    Email
    mustafasenolakin@gmail.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Nilgün Altuntas, Proff
    Organizational Affiliation
    Ankara Bilkent Central Hospital, Neonatal Unit
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Suna S Oguz, Proff
    Organizational Affiliation
    Ankara Bilkent Central Hospital, Neonatal Unit
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Mustafa S Akin, Specialist
    Organizational Affiliation
    Ankara Bilkent Central Hospital, Neonatal Unit
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided
    IPD Sharing Plan Description
    No agreement yet to share with other researchers

    Learn more about this trial

    Comparison of the Effects of Oral Stimulation and Non-nutritive Sucking Practices

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