Under construction — an early preview; content and design will change.
Sleep Health Data Commons Sleep Health Data Commons
ARPA-H REST program · led from Stanford

Building toward millions of nights of sleep, ready to learn from.

A national commons of de-identified clinical sleep data — polysomnography, EEG, home sleep tests, brain imaging and longitudinal health records — harmonized to common standards and open to credentialed researchers.

Two nights of sleep EEG from two 36-year-old women, each a hypnogram over a spectrogram on one shared time axis. The first night has younger-looking sleep: strong slow-wave power low in the spectrogram and a clear band of sleep spindles near 13 hertz. The second has older-looking sleep: visibly weaker slow waves and fewer spindles.

Two women, both 36. From a single night of sleep EEG, one brain shows the strong slow waves and spindles of a younger brain while the other shows the weaker, sparser patterns more common decades later — a difference researchers can read as a brain-health score. Measuring it across millions of nights is what the Commons is for. A research measure, not a diagnosis (Sun et al., 2019). De-identified data.

The Commons, as it grows

These are program goals. Confirmed figures will be published here before launch.

30
Health systems contributing
Goal
1M+
Patients represented
Goal · placeholder
5M+
Nights of recordings
Goal · placeholder
5
Data modalities, in 2 open standards (BIDS, OMOP)

What’s inside

Clinical data as collected, then harmonized: signals and imaging in BIDS, health records in OMOP CDM v5.4.

Polysomnography

Attended overnight sleep studies: EEG, EOG, EMG, airflow, effort, oximetry, with staging.

BIDS

EEG

Routine, ICU continuous, and epilepsy-monitoring EEG — a spectrum of acuity in one place.

BIDS

Home sleep tests

Portable airflow, effort and oximetry recordings from the home setting, at population scale.

BIDS

Brain imaging

Structural and other MRI linked to sleep and EEG for the same patients where available.

BIDS

Longitudinal health records

Diagnoses, medications, labs and encounters over time, so sleep findings connect to outcomes.

OMOP CDM v5.4

Linked across modalities

Where a patient has studies in more than one modality, the records are linked, so a night of sleep can be studied alongside imaging and clinical course.

Open source

The code, not just the data

Explore the algorithms behind the Commons — 85 open-source tools for analyzing sleep and EEG data, from automated staging and spike detection to brain-age and outcome models. Each links to its code, and many to the dataset it was built on.

Browse the analysis code →

How it works

01

Health system contributes

A site sends its archived sleep studies, EEG, imaging and linked health records.

02

Stanford de-identifies centrally

Records are de-identified in one secure place, with per-patient date shifting.

03

Harmonized to standards

Everything is converted to BIDS and OMOP CDM v5.4 so sites can be analyzed together.

04

Researchers analyze

Credentialed researchers query and analyze the Commons through bdsp.io.

For researchers

Study sleep at national scale

  • Pooled clinical sleep data across many health systems and levels of acuity.
  • Signals and imaging in BIDS, health records in OMOP CDM v5.4 — analysis-ready.
  • Access by credentialing and a data use agreement, through bdsp.io.
Request data access
For health systems

Contribute, and get your data back harmonized

  • We handle de-identification and conversion centrally; your effort is kept light.
  • You receive your own data harmonized to BIDS and OMOP, plus the conversion code.
  • Your patients’ privacy is protected under a single IRB and a data use agreement.
Talk to us about contributing

Privacy and trust

Privacy is the project’s promise. It is built into how the Commons is run, not added on.

De-identification

Direct identifiers are removed, and each patient’s dates are shifted by a consistent per-patient offset, so timelines stay internally accurate without revealing real dates.

Single IRB review

The program operates under a single IRB of record (BRANY), so oversight is consistent across every contributing site.

Stanford’s high-risk data environment

Data are handled in Stanford’s secured environment for high-risk data, with controlled, auditable access.

Credentialed access, no re-identification

Researchers are credentialed and agree to a data use agreement that forbids any attempt to re-identify individuals.

A growing national network

Each point is a contributing health system; points fill as sites join. Institutions are named only with their permission.

Joined    Goal

Placeholder network graphic (concept B). A geographic U.S. map will replace this once sites are confirmed.