NCT07290179

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

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
35

participants targeted

Target at P25-P50 for all trials

Timeline
7mo left

Started May 2026

Shorter than P25 for all trials

Status
not yet recruiting

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 Progress3%
May 2026Dec 2026

First Submitted

Initial submission to the registry

December 6, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

December 18, 2025

Completed
4 months until next milestone

Study Start

First participant enrolled

May 1, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

May 1, 2026

Status Verified

April 1, 2026

Enrollment Period

6 months

First QC Date

December 6, 2025

Last Update Submit

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

Age8 Years - 12 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)
Sampling MethodNon-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.

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

Feeding Behavior

Condition Hierarchy (Ancestors)

Behavior, AnimalBehavior

Study Officials

  • Hanim E Diktas, PhD

    Pennington Biomedical Research Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Hanim E Diktas, PhD

CONTACT

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