Recruiting

Wearable Device

Sponsor:

Northwestern University

Code:

NCT06118528

Conditions

Wearable Electronic Device

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Interventions

Blur Obfuscation

Cartoon Obfuscation

Edge Obfuscation

No Obfuscation (raw)

Study Details

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.

Conditions

Wearable Electronic Device

Study ID

NCT06118528

Start date

Sep 4, 2024

Status verified date

May, 2026

Completion date

Oct, 2026

Anticipated

Primary completion date

Sep, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

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

Study Design

Enrollment

72 participants

Anticipated

Allocation

Randomized

Intervention Model

Crossover

Primary purpose

Basic Science

Interventions and Outcome Measures

Arms

experimental: Blur Obfuscation

experimental: Edge Obfuscation

experimental: Cartoon Obfuscation

experimental: No Obfuscation (Raw)

Interventions

Blur Obfuscation

Blurring is applied to the RGB images.

Cartoon Obfuscation

Cartoonization is applied to the RGB images.

Edge Obfuscation

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

No Obfuscation (raw)

No editing is performed on the RGB images.

Primary outcome measure

  • Daily wear time [ Time Frame: 7 days ]

Central Contacts and Locations

Locations

Northwestern University

Recruiting

Chicago, Illinois, United States, 60611

More Information

Sponsor

Northwestern University

Last update posted

May 7, 2026

Last verified

May, 2026

Keywords

  • Wearable
  • Electronic
  • Device
  • Behavior
  • Eat
  • Privacy
  • Camera
  • Obesity
  • Obfuscation
  • Filter
  • Cartoon
  • Blur
  • Raw
  • Edge
  • Burden
  • Wearer
  • Bystander
  • Monitor
  • BMI
  • Calories
  • Tool
  • Algorithm
  • RGB
  • Thermal
  • Data
  • Health
  • Chest

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Northwestern University on 2026-05-07.