Human Factors Validation and Usability Testing of the IKE Age-Gating System
Completed
Conditions studied: Vaping, Underage
In brief
A multi-center human factors validation study to demonstrate the function of the IKE Bluetooth system on a chip (SoC) and mobile applications ability to age-gate a device, accurately identify an individuals age, race/ethnicity, and gender, and asses the usability of the IKE System.
Key facts
- Study ID
- NCT06952569
- Run by
- IKE Tech
- People needed
- 102
- Starts
- 2025-02-18
- Expected to finish
- 2025-03-30
- Last updated by the study team
- 2025-05-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Currently live in proximity to one of the four central location sites
- Ages 18 and older
- Have a valid driver's license or US government-issued identification with picture
- Currently use a smartphone with an iOS (Apple) or Android operating system
- Indicate somewhat (3), very (4), or extremely (5) comfortable using smartphone applications on intake questionnaire
- Able and willing to comply with all study requirements
- Review and sign informed consent
You may not qualify if…
- Under 18 years of age
- Among 21-64 years of age, do not currently use cigarettes or vape products
- Do not own or use a smartphone with an iOS (Apple) or Android operating system
- Unable to download any smartphone application
- Employees of or household member employed in advertising/marketing, market research, healthcare, legal field, news and media, or local, state or US Federal government to minimize bias and to protect any proprietary product information that will be disclosed in the study
Where it is running
- Alder Weiner, MARC Research facility partner — Los Angeles, California, United States
- Focus Center, MARC Research facility partner — Chicago, Illinois, United States
- L&E Research, MARC Research facility partner — New York, New York, United States
- Creative Consumer Research, MARC Research facility partner — Houston, Texas, United States
Full record on ClinicalTrials.gov
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