About this trial
This randomized clinical trial aims to evaluate the effectiveness of an oral stimulation program to improve sucking in preterm neonates hospitalized in the NICU. The study compares two groups: one receiving the intervention from a physiotherapist and the other from trained parents. The stimulation program includes 4 extraoral and 4 intraoral exercises applied once daily for 14 consecutive days. The primary outcome is improvement in the POFRAS score. Secondary outcomes include the time to exclusive oral feeding, nasogastric tube withdrawal, weight at discharge, hospital stay duration, and parental adherence. This study addresses the potential role of parent participation in neonatal rehabilitation in public hospitals with limited human resources.
Eligibility criteria
Qualifiers
Neonates with corrected gestational age of 34 to 36 weeks
Clinically stable to receive oral stimulation
Informed consent obtained from parents or legal guardians
Disqualifiers
Orofacial congenital malformations
Severe neuromuscular disease
Conditions contraindicating oral feeding
Trial design
Treatments tested in this trial
- Parental Oral Stimulation Protocol
- Physiotherapist-led Oral Stimulation