NCT06704971

Brief Summary

Neuropsychiatric symptoms (NPS) refer to a range of mental and emotional issues that can be observed through how patients move, perform daily tasks, and express feelings on their faces. In this study, the investigators want to find ways to accurately and unobtrusively track these symptoms in people's homes over time. Our goals are to note when these symptoms happen, predict potential problems, and gather clear data to help doctors make accurate diagnoses. To do this, the investigators will first collect information from participants who have in-home sensors. the investigators will then use special computer programs that can recognize everyday activities and identify features that connect to scores from the Mild Behavioral Impairment Checklist (MBI-C). These scores will be compared to a questionnaire (NPIQ) filled out by caregivers or family members, along with any relevant information from doctors about the patients' symptoms. The investigators aim to see how these features can help differentiate between types of NPS, such as mood changes and agitation. Finally, the investigators will create a dashboard for doctors that summarizes the patterns of these symptoms in patients, making it easier to monitor and manage their mental health.

Trial Health

75
On Track

Trial Health Score

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

Enrollment
25

participants targeted

Target at below P25 for all trials

Timeline
6mo left

Started Oct 2024

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress76%
Oct 2024Dec 2026

Study Start

First participant enrolled

October 1, 2024

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

November 21, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

November 26, 2024

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2025

Completed
1.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2026

Expected
Last Updated

May 18, 2026

Status Verified

April 1, 2026

Enrollment Period

1.1 years

First QC Date

November 21, 2024

Last Update Submit

May 14, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • develop a personalized and clinically interpretable NPS assessment system

    Assessing NPS relies primarily on clinician observation \& interviews with caregivers, usually within brief \& infrequent clinical visits. Precise assessment and monitoring methods would incorporate objective, patient- \& caregiver-friendly, real-time tools and provide reliable \& frequently captured data. We aim to create a system that can monitoring individual and subsyndromes of NPS; and detect early changes in NPS by automatically quantifying \& detecting relevant behavioral abnormalities based on both intra- \& inter-individual comparisons. Our approach is a video sensor, information processing, \& alert system that utilizes in-home cameras \& ambient sensors with video features that can recognize \& track behaviors securely, pre-defines domains involved in a behavior; personalizes the results by assessing the individual's behavioral norms and the home environment; and analyzes, learns, and provides explainable items from different modalities of data: time, location, video, and audio.

    2 year

  • NPS Clinical Dashboard

    Overall, the investigators envision the clinical dashboard as a transformative tool that delivers clear and comprehensive data on each individual. Therefore enhancing the quality of diagnosis of NPS for individuals, leading to better patient interventions and more effective long term management strategies.

    1 year

Secondary Outcomes (1)

  • generate Data and support for a large-scale study or clinical trial within the context of an R01.

    2 years

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Older Adults - 65+

You may qualify if:

  • Age 65+ years old
  • Any age and ethnicity.
  • With or without, or at risk of mild to moderate dementia and healthy controls.
  • Availability of a study partner (informant) who has contact with the patient at least once a week (this can also be the surrogate/LAR but does not necessarily have to be)

You may not qualify if:

  • Those with severe mobility impairments
  • participants in non-home settings (skilled nursing facilities, etc.).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Clinical Excellence Research Center

Palo Alto, California, 94304, United States

Location

Related Publications (1)

  • Gould CE, Davis CH, Schuz N, Lin FV, Samus QM, Terada T, Daniel M, Tee S, Adeli E. Designing AI-Enabled Video Monitoring Clinician Dashboard for Neuropsychiatric Symptoms: A Survey of User Needs. Am J Geriatr Psychiatry Open Sci Educ Pract. 2026 Mar;9:46-51. doi: 10.1016/j.osep.2026.01.001. Epub 2026 Feb 8.

MeSH Terms

Conditions

Cognitive DysfunctionAlzheimer DiseaseDementiaMemory Disorders

Condition Hierarchy (Ancestors)

Cognition DisordersNeurocognitive DisordersMental DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesTauopathiesNeurodegenerative DiseasesNeurobehavioral ManifestationsNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Ehsan Adeli, PhD

    Stanford University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Asst. Professor

Study Record Dates

First Submitted

November 21, 2024

First Posted

November 26, 2024

Study Start

October 1, 2024

Primary Completion

October 30, 2025

Study Completion (Estimated)

December 30, 2026

Last Updated

May 18, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations