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NCT Number: NCT06118528

EAT: A Reliable Eating Assessment Technology for Free-living Individuals

This study utilizes a small, privacy-conscious wearable device intended to monitor human behaviors. The device is worn around the neck, capturing the wearer's head and upper torso within its field of view, and records color images without audio. Participants visit the lab for consent, device training and recording of several activities using the device. Participants will then take the device home and wear it during their normal schedules for four "active" weeks. During each active week, participants will wear the device, keep a log of all food and drink items consumed throughout the day and participate in unscheduled phone calls with a dietitian. A "washout" week occurs in between each active week in which participants do not need to complete any study tasks. Alongside the device, we have included three privacy filters (blur, edge, and avatar) capable of obscuring faces and objects seen in the device-captured images. All participants will be subject to unfiltered recording during their first week followed by a different filter each following active week in a random order. At the start of each active week, participants view an example of what their recorded images will look like that week (given the privacy filter). At the end of the seven weeks, participants will return the device and provide the lab with feedback on the design of the device and its privacy-preserving features.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Northwestern University

Chicago, Illinois, 60611, United States

Location status: Recruiting

Location contact

Nabil Alshurafa, PhD

CONTACT

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • BMI greater than or equal to 18.5
  • Chicago metropolitan area resident
  • Able to speak, read and write in English
  • Has a valid phone number
  • Owns a smartphone
  • Has access to a computer

Exclusion criteria

  • Pregnant or breastfeeding individuals
  • Experienced significant weight loss/gain in the last three months (25 lbs or more)
  • Diagnosed with or has a family history of genetic obesity syndromes (e.g., Prader-Willi, Bardet-Biedl, Cohen Syndrome)
  • Member of household enrolled in the study

Treatment and study plan

Blur Obfuscation

Behavioral

Blurring is applied to the RGB images.

Cartoon Obfuscation

Behavioral

Cartoonization is applied to the RGB images.

Edge Obfuscation

Behavioral

A black background and simple outlines of objects/people are applied to the RGB images.

No Obfuscation (raw)

Behavioral

No editing is performed on the RGB images.

Primary outcomes

  1. Daily wear time

    Time frame: 7 days

Secondary outcomes

  1. Self-report acceptability

    Time frame: 7 days

Study contacts

Contact information is provided by the study sponsor or research team.

Bonnie Nolan

CONTACT

[email protected]

3125031216

Nabil Alshurafa

CONTACT

[email protected]

3125034517

Sponsors and collaborators

Lead sponsor

Northwestern University

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Registry information

Acronym: EAT

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Nov 7, 2023
Registry last updated
May 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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