Trial · NCT07883707
Parent-Facilitated Early Oral-Sensory Experience in the NICU for Feeding Outcomes
NCT07883707, Not applicable, Not yet recruiting, Boston College
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Parent-Facilitated Early Oral-Sensory Experience in the NICU for Feeding Outcomes. Trials, record NCT07883707. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07883707
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Parent-Facilitated Early Oral-Sensory Experience in the NICU for Feeding Outcomes
- NCT number
- NCT07883707
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 60 participants, estimated
- Lead sponsor
- Boston College
- Conditions
- Premature Birth, Infant, Premature, Infant, Very Premature
- Interventions
- Parent-Facilitated Early Oral-Sensory Experience (PEOE)
- First posted
- 2026-10-20
- Last updated
- 2026-10-20
Source ClinicalTrials.gov
Registered outcomes21
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Study Feasibility and Acceptability Rates | From screening through NICU discharge (up to 6 weeks after enrollment). | Composite measure of study feasibility evaluated by overall eligibility rate, recruitment rate, enrollment rate, retention rate, and intervention protocol completion rate. |
| Primary | Infant Short-Term Heart Rate Response Across Intervention Sessions | Weekly from the first week of enteral feeding through oral feeding initiation (up to 6 weeks post-enrollment) | Change in mean heart rate in beats per minute (bpm) and variability (coefficient of variation) measured from pre-feeding baseline (30 minutes prior) to during the PEOE intervention session and 30 minutes post-intervention. |
| Primary | Infant Short-Term Respiratory Rate Response Across Intervention Sessions | Weekly from the first week of enteral feeding through oral feeding initiation (up to 6 weeks post-enrollment) | Change in mean respiratory rate (breaths per minute) and variability (coefficient of variation) measured from pre-feeding baseline (30 minutes prior) to during the PEOE intervention session and 30 minutes post-intervention. |
| Primary | Infant Short-Term Oxygen Saturation Response Across Intervention Sessions | Weekly from the first week of enteral feeding through oral feeding initiation (up to 6 weeks post-enrollment) | Change in mean oxygen saturation (SpO2) percentage and variability (coefficient of variation) measured from pre-feeding baseline (30 minutes prior) to during the PEOE intervention session and 30 minutes post-intervention. |
| Primary | Infant Short-Term Heart Rate Variability (High-Frequency HRV) Across PEOE Intervention Sessions | Weekly from the first week of enteral feeding through oral feeding initiation (up to 6 weeks post-enrollment) | Change in high-frequency heart rate variability (HF-HRV in ms2) measured from pre-feeding baseline (30 minutes prior) to during the PEOE intervention session and 30 minutes post-intervention. |
| Primary | Infant Short-Term Heart Rate Variability (SD12 Ratio) Across Intervention Sessions | Weekly from the first week of enteral feeding through oral feeding initiation (up to 6 weeks post-enrollment) | Change in Poincare nonlinear ratio (SD12) measured from pre-feeding baseline (30 minutes prior) to during the PEOE intervention session and 30 minutes post-intervention. |
| Primary | Infant Heart Rate Response During Feeding Near Discharge | Assessed during a single feeding observation during the discharge week (approximately 2 to 6 weeks post-enrollment) | Change in mean heart rate (bpm) and variability (coefficient of variation) measured from 30 minutes pre-feeding baseline to during feeding and 30 minutes post-feeding. |
| Primary | Infant Respiratory Rate Response During Feeding Near Discharge | Assessed during a single feeding observation during the discharge week (approximately 2 to 6 weeks post-enrollment) | Change in mean respiratory rate (breaths per minute) and variability (coefficient of variation) measured from 30 minutes pre-feeding baseline to during feeding and 30 minutes post-feeding. |
| Primary | Infant Oxygen Saturation Response During Feeding Near Discharge | Assessed during a single feeding observation during the discharge week (approximately 2 to 6 weeks post-enrollment) | Change in mean oxygen saturation (SpO2) percentage and variability (coefficient of variation) measured from 30 minutes pre-feeding baseline to during feeding and 30 minutes post-feeding. |
| Primary | Infant Heart Rate Variability (High-Frequency HRV) During Feeding Near Discharge | Assessed during a single feeding observation during the discharge week (approximately 2 to 6 weeks post-enrollment). | Change in high-frequency heart rate variability (HF-HRV in ms2) measured from 30 minutes pre-feeding baseline to during feeding and 30 minutes post-feeding. |
1 to 10 of 21Source ClinicalTrials.gov
See all 21 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants1
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years |
|---|---|---|---|---|---|
| R21HD119389 | Parent-Facilitated Early Oral-Sensory Experience Program: Enhancing NICU Outcomes Through a Family-Centered Feeding Approach | Park, Jinhee | BOSTON COLLEGE | EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT | 2026 |
Source NIH RePORTER
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07883707
GET https://conductscience.org/api/trials/v1/NCT07883707/registered?page=2