Evaluating the Validity and Feasibility of a Smartwatch-based Eating Detection System to Passively and Automatically Detect Eating Events in Child-parent Dyads
1 other identifier
observational
35
0 countries
N/A
Brief Summary
This study will test the validity and feasibility of an smartwatch-based system to detect eating and drinking events in both laboratory and free-living conditions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started May 2026
Shorter than P25 for all trials
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
First Submitted
Initial submission to the registry
December 6, 2025
CompletedFirst Posted
Study publicly available on registry
December 18, 2025
CompletedStudy Start
First participant enrolled
May 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
May 1, 2026
April 1, 2026
6 months
December 6, 2025
April 29, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Accuracy and Performance of Smartwatch-based Eating Detection System in Controlled Conditions
Accuracy and performance of smartwatch-based system for detecting eating and drinking events compared to video-coded ground truth during a controlled laboratory conditions. Metrics include: Precision (proportion of correctly detected eating events among all detected events), Recall/Sensitivity (proportion of actual eating events detected), Specificity (proportion of non-eating events correctly identified as non-eating) F1-score (harmonic mean of precision and recall), Overall accuracy (proportion of correct classification).
During the controlled laboratory session (Day 1).
Adherence to Smartwatch Protocol
Proportion of families meeting adherence criteria, defined as both parent and child wearing the smartwatch during eating on at least 2 of 3 days and the parent responding to ≥75% of EMA prompts related to smartwatch charging and app functionality.
During the free-living phase (Days 2-4).
Interventions
Participants (child-parent dyads) will wear a smartwatch on their dominant hand during a laboratory session and for three days in free-living conditions. In the lab, dyads will perform eating-related activities (e.g., eating with utensils, eating with hands, drinking) and non-eating activities (e.g., walking, writing, brushing teeth) while being video recorded for ground truth validation. Parents will receive a 20-minute training on using Ecological Momentary Assessment (EMA) prompts to record meal and snack times and will respond to EMA reminders during the free-living period. Adherence will be monitored through smartwatch wear time and EMA response rates.
Eligibility Criteria
A sample of 35 dyads (35 parents and their 8-12 years old children) will be recruited from the Baton Rouge, LA area.
You may qualify if:
- Parents or caregivers (18-70 years) who have children aged 8-12 years
- Child is willing and able to wear smartwatch during school hours (have not restrictions in the school setting)
You may not qualify if:
- Any condition or circumstance that could impede study completion
- Child does not follow a regular eating pattern
- Child eats less than 1 meal and 1 snack in a day
- Child is restricted or allergic to the study foods
- Refusal or unable to use the smartwatch to collect data for the 3-day period in free - living conditions
- Parental refusal or unable to respond Ecological Momentary Assessment prompts
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Hanim E Diktas, PhD
Pennington Biomedical Research Center
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
December 6, 2025
First Posted
December 18, 2025
Study Start
May 1, 2026
Primary Completion (Estimated)
November 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
May 1, 2026
Record last verified: 2026-04