Our office will be closed Friday, July 3rd in observance of American Independence Day. We will reopen at regular business hours on Monday, July 6th.
ActiGraph's Response to Novel Coronavirus (COVID-19) - June 25th Update
ActiGraph employees are working remotely until July 13th, 2020. Shipping delays should be expected during this time.
CentrePoint Insight Watch
Medical-Grade Actigraphy Monitoring, Redefined
The compact and stylish CentrePoint Insight Watch captures and records continuous high-resolution raw acceleration data to provide objective, real-world physical activity, mobility, and sleep measures, in near real time.Contact Sales Download Flyer
Declaration of Conformity
U.S. federal law restricts this device to sale by or on the order of a physician.
The CentrePoint Insight Watch captures and records high resolution raw acceleration data, which are converted into a variety of objective activity and sleep measures using publicly available algorithms that were developed and validated by members of the academic research community. Available measures include:
- Raw Acceleration (G's)
- Energy Expenditure
- MET Rates
- Physical Activity Intensity
- Activity Bouts
- Sedentary Bouts
- Sleep Latency
- Total Sleep Time
- Wake After Sleep Onset
- Sleep Efficiency
High-Resolution Raw Data
A triaxial MEMS accelerometer captures high-resolution raw data, sampled up to 256 Hz, to support the development of novel endpoints related to real-world activity, mobility, and sleep behaviors.
Real-Time Data Access
Used in conjunction with the CentrePoint Data Hub or mobile application, captured data is passively transmitted to the cloud for near real-time detection of compliance issues and potential data trends.
With its compact and stylish design and easy-to-read, backlit time and date display, the CentrePoint Insight Watch looks and feels like a consumer smart watch.
Optimized User Experience
Single push button interface, passive data capture and transfer, and a long* battery life help to simplify and enhance the patient experience.
30-Day Battery Life
An extended battery life minimizes the burden of complicated charging protocols during long periods of data collection.
Standard interchangeable wristbands can be customized to improve patient satisfaction, comfort, and compliance.
The cloud-based CentrePoint technology system includes an ecosystem of hardware and software tools that capture and manage real-world patient data collected during a clinical trial or research study.
CentrePoint Insight Watch
The stylish and comfortable Insight Watch captures and records continuous, high resolution raw acceleration data.
CentrePoint Web Portal
This secure, permissions-based web portal provides instant access to near real-time patient outcomes and raw data files, site performance details, and overall study progress.
CentrePoint Data Hub
This communication gateway securely transmits data collected by the CentrePoint Insight Watch from the patient’s home to the CentrePoint cloud.
An available API makes it possible to integrate ActiGraph outcomes directly into our clients’ proprietary or third party EDC platforms.
1.97 x 1.35 x 0.41 in
USB/Bluetooth® LE 5
IP57 1 meter, 30 minutes
The CentrePoint Insight Watch is fully backward compatible with previous device models to ensure data comparability for our existing clients.
The CentrePoint Insight Watch is an FDA cleared Class II medical device within the United States and a Class I non-measuring medical device within the European Union that abides by the regulatory requirements listed below:
EU Directives Compliant:
- Medical Devices Directive 93/42/EEC
- Radio Equipment Directive 2014/53/EU
- RoHS Directive 2011/65/EU Compliant
- FCC Federal Register CFR 47, Part 15, Subpart B: 2017
- FCC Part 15, Subpart C, Section 15.249
- ICES-003 Interference Causing Equipment Standards for a Digital Apparatus
- RSS-210 Certification of Radio Apparatus
The CentrePoint Insight Watch is dust protected and water resistant up to 1 meter of water for 30 minutes in accordance with IEC 60529.
All ActiGraph products are manufactured Lead Free and are RoHS Compliant.
510(k) Cleared Class II Medical Device K181077
IEC 60601-1-2 General requirements for basic safety and essential performance