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Sensorimotor Stimulation on Oral Feeding

Efficacy of Sensorimotor Stimulation on Oral Feeding Skills for Neonates Post Hypoxic Ischemic Encephalopathy in Neonatal Intensive Care Unit

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06700135
Enrollment
30
Registered
2024-11-21
Start date
2024-11-28
Completion date
2025-01-05
Last updated
2024-11-26

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

Conditions

Neonates Post Hypoxic Ischemic Encephalopathy

Keywords

Neonates, Hypoxic ischemic encephalopathy, Sensorimotor stimulation

Brief summary

Background: Perinatal asphyxia and the resulting hypoxic-ischemic encephalopathy (HIE) are significant causes of irreversible adverse neurodevelopmental outcomes in children. Neonates and infants with HIE commonly experience difficulties in learning the oromotor skills of sucking, swallowing, and breathing. These feeding problems can lead to severe complications such as weight loss, dehydration, malnutrition, and developmental deficits. Objective: The study aims to assess the efficacy of sensorimotor stimulation intervention on oral skills in neonates with post-hypoxic ischemic encephalopathy in the neonatal intensive care unit (NICU). Methods: The study will include thirty infants with hypoxic-ischemic encephalopathy. They will be divided into two equal groups: The study group receive traditional medical treatment as well as a sensorimotor stimulation program, whereas the control group receive only traditional medical treatment

Interventions

OTHERsensorimotor stimulation program sessions

The study group, consisting of 15 neonates, received traditional medical treatment along with sensorimotor stimulation program sessions. These sessions included oral stimulation protocol, Tactile/Kinesthetic (T/K) intervention, feeding position, and oral support.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
1 Days to 120 Days
Healthy volunteers
No

Inclusion criteria

* neonates, diagnosed with post-hypoxic ischemic encephalopathy

Exclusion criteria

* Neonates with congenital anomalies affecting the oral-facial area, * or syndromes associated with developmental delays, * chronic medical complications

Design outcomes

Primary

MeasureTime frameDescription
Transition time from tube to full oral feeding- At least one-time breast feeding in a 24-hour period (Fucile et al., 2013). - Consuming eight feedings per day for two consecutive days. - Capable of consuming orally over 80% of the recommended total fluid intake within a 24-hour period (Premji etthe number of days from the commencement of the intervention to the first day of exclusive oral feeding.
Time taken to accomplish exclusive oral feedingAt least one-time breast feeding in a 24-hour period (Fucile et al., 2013). - Consuming eight feedings per day for two consecutive days. - Capable of consuming orally over 80% of the recommended total fluid intake within a 24-hour period (Premji et athis is the number of days from the beginning of oral feeding until discharge.

Secondary

MeasureTime frameDescription
Total hospital stayAt least one-time breast feeding in a 24-hour period (Fucile et al., 2013). - Consuming eight feedings per day for two consecutive days. - Capable of consuming orally over 80% of the recommended total fluid intake within a 24-hour periodthis is the number of days from the start of the oral stimulation program until discharge from the NICU.

Contacts

Primary ContactAhmed fekry Salman, PhD
a.salman@ammanu.edu.jo+962797168340

Outcome results

None listed

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