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NCT Number: NCT07035912

Parent Implemented Oral Nutrition, Eating, and Esophageal Reflexes Reintegration Protocol: RCT

Feeding dysfunction remains a major unmet challenge among neonatal ICU survivors, frequently leading to prolonged tube feeding or gastrostomy at discharge, increased healthcare utilization, substantial socioeconomic burden, and adverse neurodevelopmental outcomes. This randomized controlled trial will evaluate the innovative Parent-Implemented Oral Nutrition, Eating, and Esophageal Reflexes Reintegration (PIONEER) protocol to advance understanding of swallowing physiology and establish a safe, effective, family-centered feeding intervention. Successful completion of this study has the potential to reduce gastrostomy dependence, improve long-term health and quality of life, and transform standards of neonatal feeding care in alignment with NIH missions and priorities.

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Key information

About this study

Survival of neonatal intensive care unit (NICU) infants has improved substantially; however, chronic tube feeding, aerodigestive, and neurodevelopmental morbidities continue to rise. Disorders of Deglutition, characterized by impaired feeding and swallowing function, contribute to poor nutrition, impaired growth, prolonged hospitalization, adverse neurodevelopmental outcomes, and increased reliance on gastrostomy tube (G-tube) feeding. Effective, evidence-based interventions that promote oral feeding competence during critical develop-mental periods are urgently needed to reduce chronic tube feeding and its associated health and socioeconomic burdens.

The long-term goal of this research is to improve feeding, aerodigestive and developmental outcomes in high-risk NICU infants through biologically informed interventions. The objective of this application is to determine the efficacy and mechanisms of the Parent-Implemented Oral Nutrition, Eating, and Esophageal Reflexes Reintegration (PIONEER) protocol using feeding and aerodigestive stimulation therapy for infants at risk for G-tube placement. Safety, feasibility, and preliminary efficacy of the intervention have been established.

The central hypothesis is that targeted stimulation of aerodigestive reflex pathways during critical develop-mental windows promotes adaptive maturation of feeding-related neural and sensorimotor networks, resulting in improved aerodigestive reflex function, enhanced oral feeding competence, and reduced G-tube need. This hypothesis will be tested in a randomized controlled trial comparing the PIONEER protocol with standard care.

Aim 1: Determine the efficacy of PIONEER Protocol in improving oral feeding outcomes and reducing G-tube placement. Primary outcome will be met with improvement in oral feeding by 4 weeks and avoidance of G-tube at discharge. We hypothesize that more infants randomized to the PIONEER protocol will have improvement in oral intakes and avoidance of G-tubes at discharge versus infants receiving standard care.

Aim 2: Define the mechanistic biomarkers associated with intervention response. We will test the hypothesis that the PIONEER protocol enhances sensory-motor integration and normalizes aerodigestive reflex function compared with standard care. We will perform longitudinal HRPEM studies to identify treatment-related changes in physiological biomarkers and determine the mechanistic basis of improved feeding outcomes. Primary outcome: change in HRPEM-derived aerodigestive biomarkers from baseline to final study assessment.

The expected outcomes and impact of this project are: (1) validation of an effective parent-implemented intervention for infants at risk for chronic tube feeding; (2) identification of mechanistic biomarkers linking physio-logical adaptations to clinically meaningful feeding outcomes; and (3) establishment of a scalable, evidence-based therapy to improve feeding safety, feeding efficiency, growth, and developmental outcomes. Successful completion of this project is expected to reduce G-tube dependence, shorten NICU hospitalization, improve quality of life for infants and families, and lessen the substantial public health burden associated with feeding disorders.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Nasogastric tube fed infants on full enteral feeds
  • ≥37 and ≤46 weeks postmenstrual age at initial study
  • Presence of aerodigestive reflexes on initial pharyngoesophageal manometry.

Exclusion criteria

  • Potentially lethal congenital or chromosomal anomalies
  • Severe Neuropathology
  • Craniofacial defects (cleft lip or palate)
  • History of GI surgery, ENT surgery, or neurosurgery
  • Need for supplemental respiratory support of >2 LPM

Treatment and study plan

PIONEER Protocol

Combination Product
  • Oral nutritive stimulus with every feed (minimum 5mL)
  • Esophageal stimulation with up to 15 stimulations given at least 5 times per week with stimulation catheter
  • High resolution esophageal manometry as much as weekly if feasible throughout protocol
  • Parent biofeedback (during manometry studies) and education on at least a weekly basis with focus on their participation in oral feeding

Primary outcomes

  1. Improvement in oral feeding and absence of gastrostomy tube

    Time frame: improvement in feeding from prior to initial study to 4 weeks or discharge if sooner, gastrostomy tube at discharge

    Will compare successful outcomes of improvement in oral feeding at 4 weeks and absence of gastrostomy at discharge between the control and the intervention group

  2. Compare the change in mechanistic biomarkers between the groups

    Time frame: after 4 weeks or prior to discharge if sooner

    Will measure the difference in longitudinal change in aerodigestive biomarkers from initial to final HRPEM between the groups from the initial to the final high resolution pharyngoesophageal manometry.

Secondary outcomes

  1. Change in feeding volume at discharge

    Time frame: at discharge

    will measure the % of oral feeds prior to initial study and at discharge

  2. Length of hospital stay (LOHS) and postmenstrual age (PMA) at discharge

    Time frame: at discharge

    Compare the LOHS and PMA at discharge between the control and the intervention group.

  3. Growth

    Time frame: until 1 year corrected age

    Compare weight, length and head circumference growth between groups until 1 year corrected age between the control and the intervention group.

  4. Neurodevelopment

    Time frame: at 18-26 months corrected age

    compare available Bayley scores obtained from electronic medical records between the control and the intervention group .

  5. Longterm Feeding Outcomes

    Time frame: until 1 year corrected age

    Compare feeding method during the first year of life between the control and the intervention group.

  6. Pulmonary support at discharge

    Time frame: at discharge

    Compare the respiratory support at discharge between the control and the intervention group

  7. Parent satisfaction and stress level

    Time frame: at 4 weeks or discharge, whichever is sooner

    Will compare parent surveys done prior to initial study and after final study between the control and the intervention group

  8. Compare the change in mechanistic biomarkers within the groups

    Time frame: At four weeks or discharge whichever is sooner

    To compare the longitudinal change in esophageal and sphincteric length and region-specific contractile and relaxation integrals (mmHg.cm.sec) amongst feeding success and failure within and between groups.

Study contacts

Contact information is provided by the study sponsor or research team.

Erika K Osborn

CONTACT

[email protected]

6143556667

Patty Luzader

CONTACT

[email protected]

6143556697

Sponsors and collaborators

Lead sponsor

Nationwide Children's Hospital

Other

Registry information

Official study title

Parent-Implemented Oral Nutrition, Eating, and Esophageal Reflexes Reintegration Program Using Novel Aerodigestive Stimulation in Gastrostomy Risk Infants: RCT on Clinical and Mechanistic Outcomes

Acronym: PIONEER

Important dates

Study start
2027
Primary completion
2031
Study completion
2032
First posted
Jun 25, 2025
Registry last updated
Aug 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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