Vayu for research

The same protocol, delivered the same way, to every participant.

Breath interventions are hard to study because delivery drifts. Vayu gives you a fixed protocol on the participant's own phone or watch, timestamped adherence, and exportable session and HRV data. We're running one study already and we're open to more.

Vayu is a wellbeing app, not a medical device. Any clinical study design and ethics approval sits with your institution.

A lab or study setting
65,000+ users15+ countries4.8★ App Store64% 30-day retentionResearch backed by world-class universities and government institutions
Where we are

One study, under peer review

Backed by world-class universities and government institutions. A general adult cohort, four to six weeks. A medRxiv preprint is available on request.

N=199
participants
+28.6%
HRV
−7.4
bpm resting HR
−16%
perceived stress

What it does not yet cover: clinical populations, patient cohorts, controlled comparison against an active control, and anything longer than six weeks. Those are the gaps we would like collaborators for, and we would rather name them here than in a footnote.

What the platform gives a study

Four things that are usually the expensive part of running a breath intervention across a cohort.

Fixed delivery

Ratios, hold times, session length and cue pacing are set once and identical for every participant in an arm. No instructor variance.

Adherence you can see

Timestamped session starts, completions and drop-offs per participant ID, so adherence is measured rather than self-reported.

Arms and conditions

Multiple protocol arms in one deployment, including an active control, assigned by code at enrolment.

Exportable data

Session logs, watch-derived HRV and resting HR where available, and mood entries, exported as CSV against pseudonymous IDs you control.

How a collaboration works

The design is yours. We supply the instrument and the data, and we don't gate publication.

One
Scope the question

A call to work out whether the platform can actually answer what you want to ask, and to say so if it can't.

Two
Build the arms

We configure the protocols to your specification, including any active control, and hand you enrolment codes.

Three
You run the study

Ethics, consent, recruitment and analysis sit with your institution. We hold no participant identities.

Four
Publish either way

No approval right over findings and no embargo on a null result. We would rather know.

What we provide
Study seats at no cost for academic work, subject to scale
Protocol configuration and enrolment codes
CSV export against your pseudonymous IDs
A named technical contact for the duration
What sits with you
Study design, ethics approval and consent
Recruitment and participant support
Analysis and publication
Any clinical oversight the population requires

Tell us what you want to ask.

A short note on the population, the question and the timeline is enough to start. If the platform is the wrong instrument for it, we will say so on the first call.

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