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NCT07596186Active, not recruiting

Predict Early Cognitive Changes in a Healthy Elderly Population by Passively Recording Sensor Data From Mobile Devices

Passive Digital Monitoring for the Detection of Cognitive Decline How Patterns of Behavior May Predict Dementia and Alzheimer's

Source: ClinicalTrials.gov · Last updated 19 May 2026

Brief summary (registry, in English)

The study will recruit 100 participants aged 65+ residing in assisted living facilities. Eligible participants will undergo an initial cognitive assessment to document their baseline cognitive status using cognitive tests conducted either in their assisted living facility or at Soroka Medical Center. An app designed for research data collection (Aware-Light) will be installed on participants' mobile devices, collecting data only after participants provide consent. Over three months, the app will automatically gather sensor data, including movement data from the accelerometer, orientation data from the gravity sensor, rotation data from the gyroscope, proximity data for measuring distance from nearby objects, ambient light levels from the light sensor, and typing dynamics such as typing frequency and duration without recording actual text. The app will also track app usage, including activation, pauses, closures, background activity, notifications, and crashes, as well as air pressure through the barometer, phone capabilities through the telephony detector, and screen states such as on, locked, or off. It will log communication events such as calls and messages without recording personal details, monitor vehicle speed through the linear accelerometer, track rotation angles through the rotation detector, and identify significant movements like walking, cycling, or traveling. No typed data, such as passwords, will be collected. After one month, the research team will contact participants to ensure the app functions correctly. After three months, participants will undergo a second cognitive assessment, and the app will be uninstalled.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
98 (actual)
First submitted
13 May 2026
Start date
1 Dec 2024
Primary completion date
1 Jan 2027
Lead sponsor
Soroka University Medical Center
NCT number
NCT07596186

What you commit to

  • Study type: Observational
  • Participants enrolled: 98
  • From 1 Dec 2024 to the primary completion date, 1 Jan 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • A known diagnosis of dementia

Other

  • Uses IOS mobile.
  • Doesn't write text messages

Who the study is looking for

  • Age 65 and over
  • Clalit HMO members.
  • Without a known diagnosis of dementia
  • Uses Android mobile phones and writes text messages

Age in the registry: 65 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Soroka Medical Center
Coordinator of this site? Confirm its status
BeershebaIsraelUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.