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The effect of positioning on the transition from tube to oral feeding in preterm infants: A pilot study

The effect of positioning on the transition from tube to oral feeding in preterm infants: A pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN46659438
Enrollment
10
Registered
2006-09-29
Start date
2005-04-01
Completion date
Unknown
Last updated
2017-10-30

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

Conditions

Positioning on the transition from tube to oral feeding in preterm infants Neonatal Diseases

Interventions

This pilot study will take place on a local neonatal unit and will examine the bottle feeding skills of premature infants whilst they are being fed either an elevated side-lying position, or a traditi

Sponsors

Record Provided by the NHSTCT Register - 2006 Update - Department of Health
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: At the time of first introduction to oral feeds, preterm infants (infants born with a gestational age of 36 completed weeks or less) will be randomly allocated to either the intervention or the control group. Randomisation will be my means of sealed envelopes containing either the words elevated side-lying position or traditional position. The aim is to have five participants in each group.

Exclusion criteria

Exclusion criteria: 1. Infants will be excluded if they are medically unstable 2. Have either a cleft lip or palate 3. Have identified neurological symptoms 4. Have congenital anomalies 5. Have known maternal substance abuse 6. Are to be discharged to other wards of hospitals before full oral feeding has been established 7. Have a gestational age of 37 weeks or above 8. Are being breastfed 9. If it is not possible to explain the study adequately so that informed consent can be obtained then those infants will be excluded from the study. Informed consent will be obtained from the infants carers by either the researcher or a senior member of the nursing staff.

Design outcomes

Primary

MeasureTime frame
Not provided at time of registration

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026