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
About this trial
This is an interventional supportive care trial for Premature focused on measuring Sucking, Oral stimulation, Premature baby
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
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
NCT ID
NCT05249179
First Posted
December 11, 2021
Last Updated
February 18, 2022
Sponsor
Ankara City Hospital Bilkent
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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