NCT05547425

Brief Summary

WildCam is a wearable device that collects video data of the user's face and upper torso to capture eating behaviors. WildCam and its accompanying software is privacy conscious, meaning it utilizes a computer vision algorithm that extracts proximal features (the user's body and objects-in-hand) from the video and digitally obfuscates the distal features (background environment and entities therein) to preserve the privacy of the wearer, as well as any bystanders who may be in the device's visual field. The present study tests the impact of 3 different obfuscation techniques on acceptability, including the willingness of users to wear the device. Participants are randomly assigned to 1 of the 3 obfuscation techniques (blurring, masking, or cartooning). Participants wear the WildCam during waking hours during a 7-day period with the randomly selected obfuscation setting enabled and a 7-day period with the raw images (no obfuscation) setting. The order of these periods is counterbalanced, and the two periods are separated by a 7-day washout period during which WildCam is not worn. Structured feedback, including user burden and acceptability surveys, is collected to determine the efficacy of each obfuscation technique on increasing user acceptability, including willingness to use the WildCam device, as opposed to a video-collecting device without obfuscation.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Sep 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

May 24, 2022

Completed
4 months until next milestone

Study Start

First participant enrolled

September 20, 2022

Completed
1 day until next milestone

First Posted

Study publicly available on registry

September 21, 2022

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 21, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 21, 2023

Completed
Last Updated

October 27, 2023

Status Verified

October 1, 2023

Enrollment Period

6 months

First QC Date

May 24, 2022

Last Update Submit

October 25, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • Mean Wear Time

    Average duration in minutes of data collected per day, calculated from video time stamps

    7 days

Secondary Outcomes (1)

  • Acceptability

    7 days

Study Arms (4)

Blur obfuscation

EXPERIMENTAL

Blurring is applied to objects and people in the background of images.

Device: Blur Obfuscation

Edge obfuscation

EXPERIMENTAL

Objects and people in the background of images are replaced with an outline of the object.

Device: Edge Obfuscation

Cartoon obfuscation

EXPERIMENTAL

Blurring is applied to objects and people in the background of images and the wearer's face is concealed with cartoon faces.

Device: Cartoon Obfuscation

Raw images

EXPERIMENTAL

No editing is performed on images.

Device: Raw images

Interventions

Blurring is applied to objects and people in the background of images.

Blur obfuscation

Objects and people in the background of images are replaced with an outline of the object.

Edge obfuscation

Blurring is applied to objects and people in the background of images and the wearer's face is concealed with cartoon faces.

Cartoon obfuscation

No editing is performed on images.

Raw images

Eligibility Criteria

Age18 Years - 64 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • BMI 30 or greater
  • Chicago Metro Area resident
  • Able to speak, read, and write in English
  • Valid phone number
  • Smartphone ownership
  • Have Wi-Fi at home

You may not qualify if:

  • % or greater weight change in last 3 months
  • Medication related weight gain
  • Genetic obesity syndrome (e.g., Prader-Willi, Bardet-Biedl, Cohen Syndrome)
  • Member of household enrolled in study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Northwestern University Department of Preventive Medicine

Chicago, Illinois, 60611, United States

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Model Details: Of the 3 obfuscation settings (blur, mask, cartoon), participants are randomly assigned to 1, which they test for the first or second 7-day test period. During the remaining test period, participants use WildCam with the raw images setting. There is a washout period between each test period. The order of the test sequence is counterbalanced across participants to reduce carryover effects.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

May 24, 2022

First Posted

September 21, 2022

Study Start

September 20, 2022

Primary Completion

March 21, 2023

Study Completion

March 21, 2023

Last Updated

October 27, 2023

Record last verified: 2023-10

Data Sharing

IPD Sharing
Will not share

Locations