Evidence / current stage

What did we build, and how did we test it?

WISAM connects signal processing, safety logic, and demonstration caregiver and responder screens. We ran automated software tests and evaluated GPS and HRV on separate public-data tasks. This page explains the results and what can be learned from them.

01 / What is built

A working software path from signals to screens.

The software receives signals, combines component results, and displays status and alerts in demonstration caregiver and responder interfaces.

01

Software pipeline

The prototype connects telemetry ingestion, component scoring, risk fusion, and caregiver/responder demonstration interfaces.

End-to-end refers to the software prototype with simulated inputs, not a complete wearable-to-care deployment.

Prototype
02

Caregiver interface

A caregiver interface presents status, alerts, and context for review and action.

Real prototype UI; several values and controls remain demo/static or local state, and live location is not connected end-to-end.

Prototype
03

Responder flow

A responder-facing emergency profile prototype provides limited context in a demonstration flow.

A demonstration flow with sample data; it is not connected to live emergency services.

Prototype

02 / What has been evaluated

GPS and HRV were tested separately.

GPS was tested on routes with heuristic labels; HRV was tested on one-minute sleep-apnea windows. Neither task measures dementia wandering or the effectiveness of the full product.

03 / How we evaluated the components

The task behind each number

01 / Component evaluation

GPS · GeoLife

Target: heuristic abnormal-route labels on public mobility trajectories.

1,896 trajectories from 40 general users; 1,395 training and 501 test trajectories with a user-disjoint split. Random Forest precision 0.4471, recall 0.7686, F1 0.5653 against heuristic abnormal labels.

GeoLife contains no dementia wandering labels. These are component proxy-task metrics, not clinical product accuracy or advance prediction.

02 / Component evaluation

HRV · PhysioNet Apnea-ECG

Target: apnea labels used as a proxy anomaly task on one-minute HRV windows.

2,964 one-minute windows; 945 test windows from two held-out records. Saved estimator: precision 0.8981, recall 0.6936, F1 0.7827, ROC-AUC 0.8931. Baseline construction used known-normal windows including within held-out records; record selection was not prospective.

General adult sleep-apnea data, not dementia patients; these are proxy-task component metrics, not clinical dementia or apnea diagnosis.

03 / Prototype

IMU · feasibility only

Synthetic scaffold data exercise the fall and gait software path.

The current fall and gait model uses synthetic scaffold data; its synthetic test scores are not public accuracy evidence.

Synthetic feasibility only; no proven fall detection or prevention performance.

Source review: · GPS evaluation report · HRV evaluation report

04 / Results

WISAM / Evidence

WISAM Evidence Dashboard

Select a category to see what was tested, the result, and the limit of that result.

Evidence class / Engineering verificationReported verification run · 7 September 2026
72Automated tests
45Backend/API
27AI services
What this means

45 backend/API tests plus 27 AI-service tests, rechecked 7 September 2026. Frontend typechecks are excluded. Engineering test coverage, not clinical or field validation.

Evidence class / Component evaluationEvidence reviewed
Component task scores · scale 0–1
Precision0.4471
Recall0.7686
F1 score0.5653
1,896Trajectories
Dataset & task

GeoLife public mobility trajectories. Heuristic abnormal-route labels; user-disjoint train/test split.

What this means

GeoLife contains no dementia wandering labels. These are component proxy-task metrics, not clinical product accuracy or advance prediction.

Evidence class / Component evaluationEvidence reviewed
Component task scores · scale 0–1
ROC-AUC0.8931
Precision0.8981
Recall0.6936
F1 score0.7827
2,964One-minute windows
Dataset & task

PhysioNet Apnea-ECG. One-minute sleep-apnea proxy windows; two held-out test records.

What this means

General adult sleep-apnea data, not dementia patients; these are proxy-task component metrics, not clinical dementia or apnea diagnosis.

Evidence class / Prototype / feasibilityEvidence reviewed
An IMU/motion pathway is present in the prototype risk pipeline.
Dataset & task

Synthetic scaffold data. Fall and gait pathway feasibility in the software prototype.

What this means

The current fall and gait model uses synthetic scaffold data; its synthetic test scores are not public accuracy evidence.Synthetic feasibility only; no proven fall detection or prevention performance.

05 / What this does not prove

These results do not yet show:

A technical result for one component is not a clinical result for the whole service.

  • 01Clinical effectiveness for people living with dementia
  • 02Prospectively validated wandering prediction
  • 03Production smartwatch deployment performance
  • 04Reduced caregiver burden
  • 05Reduced adverse events

06 / Next validation stage

The next test requires a real wearable.

First, connect and assess a physical wearable. Then design a controlled pilot with partners and appropriate approvals to measure reliability, alerts, usability, and the caregiver workflow. These stages are still ahead.

Explore research collaboration