Feasibility, Acceptability, and Validation of a User-friendly Diet Quality Tool in Adults From Ambulatory Nutrition Clinics
PLATE
1 other identifier
observational
122
1 country
1
Brief Summary
The study design for Perceptions and Learning About a Diet Tool (PLATE) was a prospective online dietary intake survey in adults engaged in ambulatory nutrition counseling.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Apr 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 15, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
February 15, 2025
CompletedFirst Submitted
Initial submission to the registry
July 25, 2025
CompletedFirst Posted
Study publicly available on registry
August 7, 2025
CompletedAugust 7, 2025
July 1, 2025
11 months
July 25, 2025
July 31, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Acceptability of cellphone photos
survey questions about ease of use of cellphone for photos, comfort sending photos to study team, preference for food photos for diet intake reporting in the future on Likert scale.
3 days
Secondary Outcomes (2)
Test-retest replicability
4-10 days
Validity of Penn Healthy Diet-Goals (PHD-G) survey relative to 3-day food record.
4-10 days between first food record day and following PHD-G.
Eligibility Criteria
Adults who attended nutrition counseling visit at Penn Medicine within the past 6 months.
You may qualify if:
- Adults who attended a nutrition counseling visit at Penn Medicine within past 6 months
You may not qualify if:
- No nutrition counseling visit within past 6 months, age \< 18 years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Pennsylvania
Philadelphia, Pennsylvania, 19104-4217, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Charlene W Compher, PhD
University of Pennsylvania
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
July 25, 2025
First Posted
August 7, 2025
Study Start
April 1, 2024
Primary Completion
February 15, 2025
Study Completion
February 15, 2025
Last Updated
August 7, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF
- Time Frame
- 7/25/2025-7/24/2026
- Access Criteria
- Investigators who request permission from the PI for a specific analytical question will be evaluated for potential deidentified data sharing.
Deidentified IPD may be shared upon request and approval of the authors.