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Effect of Finger Feeding

Effect of Finger Feeding on Term Newborns: A Randomized Controlled Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05928715
Enrollment
140
Registered
2023-07-03
Start date
2023-04-15
Completion date
2024-06-15
Last updated
2023-07-03

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

Conditions

Alternative Feeding Methods, Finger Feeding

Keywords

Finger Feeding

Brief summary

With the planned study, it was aimed to determine the effect of finger feeding method on newborns in term babies.

Detailed description

It was planned as a randomized controlled experimental study design. Full randomization will be performed and infants who meet the inclusion criteria will be assigned to groups by flipping a coin. On the toss of a coin, if heads came up then subject was allocated to the control group. If tails came up, then subject was allocated to the intervention group. This procedure was repeated for each mother. Within the scope of the study, Informed consent will be obtained from the parents for infants who need formula supplementation or for infants fed with expressed breast milk by the decision of the Physician in the experimental and control groups. Babies in the control group will continue to receive routine care and no intervention will be made on their feeding style. The researcher will be informed verbally and practically about the finger feeding method and the application steps to the mothers of the babies in the experimental group and to the family members who will support their feeding in baby care. In this direction, it will be ensured that expressed breast milk or formula support is given by finger feeding method.

Interventions

The newborn will receive every expressed breast milk or formula support during the day with the finger feeding method.

Sponsors

Mustela Foundation
CollaboratorUNKNOWN
Amasya University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

Mother is 18 years or older Newborns 38 weeks and older Newborns who do not have any postnatal health problems and are followed up with the mother Babies taking formula supplements Babies who have difficulty breastfeeding There is no obstacle to breastfeeding or breastfeeding

Exclusion criteria

Babies with sucking and swallowing dysfunction Babies with respiratory distress (respiratory rate over 60/min, babies with groaning, nasal wing breathing) \-

Design outcomes

Primary

MeasureTime frameDescription
Breastfeeding15 days after the start of the interventionNumber of breastfeeding per day
Expressed breast milk15 days after the start of the interventionamount of daily expressed breast milk intake
Formula intake15 days after the start of the interventionamount of daily formula consumption
finger feeding15 days after the start of the interventionnumber of finger feeding per day

Countries

Turkey (Türkiye)

Outcome results

None listed

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