Clinical Grade Physical Activity & Sleep Monitoring Solutions

Wearable technologies provide valuable insights into the real-world behavior of patients enrolled in clinical trials. Objective activity and sleep measures are important quality of life indicators that can augment patient reported outcomes to help investigators and sponsors evaluate treatment responses and make faster, better informed clinical decisions. However, the complexities of the clinical development process demand a clinical-grade technology solution that not only delivers high quality data, but is simple to deploy and manage at sites around the world.

ActiGraph Clinical Trial solutions

Our suite of FDA 510(k) cleared wearable activity monitors and cloud-based CentrePoint software platform deliver protocol-specific physical activity and sleep measures derived from high resolution accelerometer data and a selection of validated algorithms developed by members of the global academic research community.

Link, CentrePoint Sync, and CentrePoint MVPA Details
Senior Couple Walking on Boardwalk

Capture High Quality Patient Measures

  •   Daily activity profile - steps taken, kcals, and activity counts
  •   Bouts of sustained physical activity
  •   Intensity of physical activity (sedentary, MVPA, etc.)
  •   Sleep score, including sleep time and efficiency
  •   Patient wear time compliance
  •   High resolution raw accelerometer data

Stay Connected to Your Sites & Subjects

By leveraging the power and flexibility of cloud and mobile technologies, our CentrePoint platform provides instant, role-based visibility of sites, patients, and overall study progress from any web-connected device. Real-time information about wear compliance, patient outcomes, and site performance helps your team identify and address issues early on, to optimize data quality, drive efficiency, and inform clinical decisions.

Researchers Working with CentrePoint

Clinical Trial Support Services

We’ve partnered with major pharmaceutical companies and contract research organizations (CROs) in dozens of clinical trials across various phases, therapeutic areas, and patient populations. Because we understand the challenges of implementing new technologies within the complex drug development environment, we offer a variety of support services to make sure activity monitor deployment runs smoothly and captured data is accurate and clinically relevant.

Subject Matter Expert Consulting

We’ve developed a network of subject matter experts (SME) that can assist with protocol development, device deployment, endpoint validation, algorithm development, and physical activity and sleep analysis during the trial or after Database Lock. Our SME partners have extensive experience with ActiGraph products and the interpretation of activity and sleep metrics.

Data Configuration & Transfers

Our Data Management team can configure your study data to match the specifications of the sponsor or CRO Data Management Team. This includes filtering the data to provide protocol-specific endpoints to the EDC system.

In-Trial Data Screening

Help guarantee the integrity of your study data with in-trial data screening. Tiered services include wear compliance verification, site error checks and queries, and monitoring changes in activity or sleep levels.

Site Shipping Logistics

Eliminate the hassle and inefficiencies of activity monitor disbursement and management. We’ll ship activity monitors to each site, monitor study inventory, and handle device repair and replacements.

Site Training

Let our Accounts Management team train your site personnel with protocol-specific CentrePoint training sessions, performed either on-site or via telecomm.

Choose a Technology Partner with Unmatched Expertise

With over a decade of large-scale, multi-site study expertise, ActiGraph is your premier provider of clinical grade physical activity monitoring solutions.
Please contact us to learn more or discuss your specific activity monitoring needs.

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