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
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Soroka Medical Center Coordinator of this site? Confirm its status | Beersheba | Israel | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.