- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06771778
Advancing the Role of the Neonatal Registered Dietitian Nutritionist
Elevating the Neonatal Dietitian for the Future: Insights From the Experts Themselves
This observational study aims to identify the needs, engagement levels, and expertise of NICU RDNs and provide insights into their job satisfaction and career longevity.
This cross-sectional examination was conducted in March - April 2024 using a national, online, IRB-approved survey sent to established Neonatal and Pediatric Dietitian practice groups. A Qualtrics link was provided for current and former NICU RDNs to complete a 10-minute online survey.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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Florida
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Miami, Florida, United States, 33199
- Florida International University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria: Current and former Neonatal Registered Dietitian(s)
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Exclusion Criteria:
Practice outside of the USA and Canada.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Newborn Intensive Care Unit (NICU) Registered Dietitian(s)
Current or former Newborn Intensive Care Unit (NICU) Registered Dietitian(s)
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A Qualtrics link was provided for current and former NICU RDNs to complete a 10-minute online survey that provided an optional gift card for completion.
Part 1 of the survey had eight questions, and part 2 had eleven additional questions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Exploratory Neonatal Registered Dietitian Opinions
Time Frame: Time Frame: March 28 - April 2, 2024
|
Description: 253 current (n=206) and former (n=47) NICU RDNs completed the online questionnaire.
Multiple choice, observational data collected.
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Time Frame: March 28 - April 2, 2024
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Alayne M Gatto, M.S., R.D.N., Florida International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- IRB-23-0559
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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