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Effect of Baby Massage on Oral Motor Skills of Premature Babies

The Effect of Baby Massage on Oral Motor Coordination Ability in Premature Babies

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06308471
Enrollment
40
Registered
2024-03-13
Start date
2021-09-01
Completion date
2023-05-01
Last updated
2024-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infant, Premature

Keywords

Oral feeding skills, Baby massage, Fucile protocol

Brief summary

This experimental research was conducted in a single-blind, block randomized controlled design type. The primary purpose of the study is to examine the effect of premature baby massage on oral motor coordination skills. The secondary aim is to evaluate the consistency of use of The Oral Feeding clinical scale in premature babies in Turkey. As a result of the power analysis, baby massage was applied to the intervention group (n = 20) and oral stimulation with the Fucile protocol was applied to the control group (n = 20). Comparative results were evaluated statistically.

Detailed description

The Effect of Baby Massage on Oral Motor Coordination Ability in Prematures Purpose: The primary purpose of the study is to examine the effect of premature baby massage on oral motor coordination skills. The secondary aim is to evaluate the consistency of use of The Oral Feeding clinical scale in premature babies in Turkey. Method: The research was a single-blind, block randomized controlled design type and data was collected between September 2021 and May 2023. Baby massage was applied to the intervention group (n=20) of the study, and oral stimulation was applied with the Fucile protocol to the control group (n=20). The applications were applied for 15 minutes every day for ten days, and oral feeding trials were video recorded. Feeding videos were evaluated by expert neonatal nurses using The Oral Feeding Scale. Descriptive statistical methods, Fisher test, chi-square analysis, dependent and independent t test, Mann Whitney U test, one-way analysis of variance, Kruskal Wallis test, Pearson and Spearman correlations were used to evaluate the research results.

Interventions

OTHERBaby massage was applied to the intervention group (n=20) of the study

The application was applied for 15 minutes every day for ten days, and oral feeding trials were video recorded. Feeding videos were evaluated by expert neonatal nurses using The Oral Feeding Scale without knowing the application group of the babies.

The application was applied for 15 minutes every day for ten days, and oral feeding trials were video recorded. Feeding videos were evaluated by expert neonatal nurses using The Oral Feeding Scale without knowing the application group of the babies.

Sponsors

Ege University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Professional nurses who evaluate nutrition do not know which group they belong to in the study. They do not know which group the premature babies are in due to their age.

Intervention model description

Baby massage was applied to the intervention group (20) of the study, and oral stimulation was applied with the Fucile protocol to the control group (20).

Eligibility

Sex/Gender
ALL
Age
1 Days to 28 Days
Healthy volunteers
Yes

Inclusion criteria

* Being between 28-33 weeks of gestation, * Not having a congenital disease, * Clinical findings are stable and normal, * It meets the readiness criteria for oral feeding, * Being fed at full dose via Oral/Nasogastric tube and having never attempted oral intake before, * It must weigh between 1000-2000 grams * Parents give their consent to participate in the research and record video.

Exclusion criteria

* Premature babies of parents who did not give consent to participate in the study, * Premature babies of parents who gave up participating in the study at any stage of the study, * Physiological stability was impaired during the data collection process; Premature babies who require oxygen support and/or mechanical respirators, * Conditions that disrupt clinical stability such as intracranial bleeding, necrotizing enterocolitis, neonatal sepsis are included in the process.

Design outcomes

Primary

MeasureTime frameDescription
time for first oral feedingup to 36th week of gestationassessment of feeding skills
time for full oral feedingup to 38th week of gestationassessment of feeding skills

Secondary

MeasureTime frameDescription
discharge timeup to 40th week of gestationtime to hospital discharge (related to feeding ability)

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026