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Effects of Oral Stimulation Performed by Parents to Improve Sucking in Neonates Hospitalized in the NICU

Effects of Oral Stimulation Performed by Parents to Improve Sucking in Neonates Hospitalized in the NICU: A Randomized Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07060573
Enrollment
32
Registered
2025-07-11
Start date
2025-07-18
Completion date
2027-02-01
Last updated
2026-02-19

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

Conditions

Premature Infant, Sucking Behavior

Keywords

Premature infant, sucking, oral stimulation, POFRAS, NICU, feeding, physiotherapy, Rehabilitation, parental involvement

Brief summary

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.

Detailed description

This single-blind, randomized clinical trial aims to compare the effectiveness of oral rehabilitation performed by trained parents versus physiotherapists to improve sucking in preterm neonates hospitalized in the NICU at the Hospital Civil de Guadalajara "Fray Antonio Alcalde," during the period July-October 2025. Eligible neonates will be randomized into two groups: Group A (Control): Intervention performed daily by a trained physiotherapist. Group B (Experimental): Intervention performed daily by the parents after structured training and supervised implementation. The oral stimulation program consists of 4 extraoral and 4 intraoral exercises designed to promote the development of sucking, swallowing, and breathing coordination. Each session lasts approximately 15 minutes and will be applied once daily for 14 consecutive days or until full oral feeding is achieved. The primary outcome will be improvement in oral feeding readiness, assessed using the validated Spanish version of the POFRAS (Preterm Oral Feeding Readiness Assessment Scale). Secondary outcomes include: achievement of exclusive oral feeding, time to withdrawal of nasogastric tube, weight gain, hospital length of stay, and parent adherence to the protocol. Randomization will use permuted blocks, and the outcome assessor will be blinded to group assignment. This study explores the feasibility and impact of parent-administered interventions in a public hospital setting with limited specialized personnel.

Interventions

BEHAVIORALParental Oral Stimulation Protocol

This intervention consists of a structured oral stimulation protocol composed of 4 extraoral and 4 intraoral exercises designed to improve oral motor function in preterm neonates. Exercises include perioral massage, stimulation of sucking reflex, and non-nutritive sucking using a pacifier. The protocol is administered once daily for 14 consecutive days. In this study arm, the intervention is performed by parents, previously trained and supervised in the neonatal unit.

BEHAVIORALPhysiotherapist-led Oral Stimulation

This intervention consists of a structured oral stimulation protocol composed of 4 extraoral and 4 intraoral exercises designed to improve oral motor function in preterm neonates. Exercises include perioral massage, stimulation of sucking reflex, and non-nutritive sucking using a pacifier. The protocol is administered once daily for 14 consecutive days. In this study arm, the intervention is performed by a licensed physiotherapist.

Sponsors

Hospital Civil de Guadalajara
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
34 Weeks to 36 Weeks
Healthy volunteers
No

Inclusion criteria

* Neonates with corrected gestational age of 34 to 36 weeks * Clinically stable to receive oral stimulation * Informed consent obtained from parents or legal guardians

Exclusion criteria

* Orofacial congenital malformations * Severe neuromuscular disease * Conditions contraindicating oral feeding

Design outcomes

Primary

MeasureTime frameDescription
Change in POFRAS Score from Day 1 to Day 14Baseline and Day 14 of interventionChange in the total score of the POFRAS scale (0-36 points), which evaluates oral feeding readiness in preterm neonates. A higher score indicates greater readiness for oral feeding.

Secondary

MeasureTime frameDescription
Time to Exclusive Oral FeedingFrom baseline to achievement of full oral feeding (up to 14 days)Number of days required for the neonate to transition from tube feeding to exclusive oral feeding without need for nasogastric support.
Weight at Hospital DischargeBaseline and Day 14 post-interventionBody weight in grams recorded at the time of NICU discharge
Length of Hospital StayFrom birth until hospital discharge, assessed up to 60 daysTotal number of days the neonate remains hospitalized in the neonatal intensive care unit (NICU) until medically cleared for discharge.
Parental SatisfactionAt Day 14 or end of interventionLevel of parental satisfaction with the intervention protocol, assessed using a 5-point Likert scale (1 = very dissatisfied; 5 = very satisfied).

Countries

Mexico

Contacts

CONTACTNelsi Alejandra Gonzalez Gonzalez, subspecialty
ngonzalez@hcg.gob.mx+5213312567344
CONTACTJose Armando Labra Zepeda, Fellow
drjosearmandolz@gmail.com+5213313249586

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026