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RecruitingNCT07290179Updated Jun 11, 2026

Evaluating the Validity and Feasibility of a Smartwatch-based Eating Detection System to Passively and Automatically Detect Eating Events in Child-parent Dyads

An observational study in Eating Behavior, sponsored by Pennington Biomedical Research Center. Recruiting at 1 site in United States. Open to participants aged 8 Years to 12 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-11.

Sponsored by Pennington Biomedical Research Center · Observational

From the registry’s dates

  • Started Jun 2026; still recruiting 5 months later.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
35
Ages
8 Years to 12 Years
Sex
All
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Study 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.

Read the detailed description

The study will: 1) determine whether the smartwatch-based system accurately detects eating events in child-parent dyads in controlled settings and 2) evaluate the feasibility and practicality of passively detecting eating events in child-parent dyads over 3 days in free-living settings. The study will include two phases. During the laboratory visit, child-parent dyads will wear the smartwatch on their dominant hand and perform activities including eating gestures. These activities will be recorded with a video camera, and the videos will be coded for the ground truth times of eating. In the second phase of the study, child-parent dyads will continue wearing the smartwatch for 3 more days in free-living conditions. In the free-living period, parents will receive personalized Ecological Momentary Assessment (EMA) prompts reminding them to activate the smartwatch.

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Conditions studied

  • Eating Behavior

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03

In context

Feeding Behavior

985 studies on the registry are indexed under Feeding Behavior; 178 are open to participants now.

This study's planned enrollment of 35 is below the median of 183 across 270 observational studies indexed under Feeding Behavior.

Browse Feeding Behavior studies →

Lead sponsor

Pennington Biomedical Research Center is the lead sponsor of 284 studies on the registry; 31 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
8 Years to 12 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

A sample of 35 dyads (35 parents and their 8-12 years old children) will be recruited from the Baton Rouge, LA area.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 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)

Exclusion criteria

Exclusion Criteria:

  • 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
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Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
35 participants (estimated)
Patient registry
No

Interventions

  • OtherSmartwatch and EMA-based eating behavior tracking

    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.

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What researchers measure

Primary outcomes

  1. 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).

    Time frame: During the controlled laboratory session (Day 1).

  2. 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.

    Time frame: During the free-living phase (Days 2-4).

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Study locations

1 of 1 sites recruiting
  • Pennington Biomedical Research Center
    Baton Rouge, Louisiana 70808, United States
    Recruiting
    • Hanim E Diktas, PhD · Contact
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07290179
Responsible party
Hanim Diktas (Principal Investigator, Pennington Biomedical Research Center) — Principal investigator
First posted
Dec 18, 2025
Start date
Jun 10, 2026
Primary completion
Nov 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Jun 11, 2026

Study contacts

Hanim E Diktas, PhD
Contact
hanim.diktas@pbrc.edu
(225) 763-2832
Hanim E Diktas, PhD
principal investigator · Pennington Biomedical Research Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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