EAT: A Reliable Eating Assessment Technology for Free-living Individuals
- Conditions
- Wearable Electronic Device
- Interventions
- Device: Edge ObfuscationDevice: Blur ObfuscationDevice: No Obfuscation (raw)Device: Cartoon Obfuscation
- Registration Number
- NCT06118528
- Lead Sponsor
- Northwestern University
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 72
- 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
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Edge Obfuscation Edge Obfuscation - Blur Obfuscation Blur Obfuscation - No Obfuscation (Raw) No Obfuscation (raw) - Cartoon Obfuscation Cartoon Obfuscation -
- Primary Outcome Measures
Name Time Method Daily wear time 7 days
- Secondary Outcome Measures
Name Time Method Self-report acceptability 7 days
Trial Locations
- Locations (1)
Northwestern University
🇺🇸Chicago, Illinois, United States