We value your privacy

We use cookies to analyze site usage and improve your experience. You can accept all, reject non-essential, or customize. See our Privacy Policy.

kindr currently serves patients in the United States only. Content is for informational purposes elsewhere.

Real-world evidence · Open methodology

The Kindr Outcomes Registry.

Most menopause telehealth companies publish testimonials. We publish protocol. This is the fixed, pre-registered standard by which Kindr Health measures and reports whether our care actually works — declared before the first result, so the results mean something when they arrive.

Read our published research →Menopause data hub

Registry status

Protocol
Published
Endpoints fixed and public below
Cohort 1
Enrolling
Opens with first prescribing cohort
First report
Pending
12 weeks after cohort 1 closes
Reporting cadence
Quarterly
Every cohort, results and nulls

No outcome figures appear on this page yet, and none will until a pre-registered cohort completes follow-up. Any clinic quoting effectiveness percentages without a cohort, a denominator, and a follow-up rate is quoting marketing, not evidence.

Pre-registered endpoints.

Declared August 1, 2026. These do not change between cohorts. If we ever add an endpoint, the addition is dated and the original list stays visible.

TierMeasureInstrumentMeasurement window
Primary endpointVasomotor symptom burden at 12 weeksMenopause Rating Scale (MRS) — hot flash / sweating itemBaseline, week 4, week 12
SecondarySleep quality changeSingle-item sleep disturbance rating (0–10)Baseline, week 4, week 12
SecondaryMood and cognitive symptom changeMRS psychological subscaleBaseline, week 12
SecondaryTreatment persistenceProportion still on therapy at 12 and 24 weeksWeek 12, week 24
SafetyAdverse events and discontinuation reasonsClinician-coded reports from our pharmacovigilance intakeContinuous

How we report.

Endpoints declared before data collection

The measures below are fixed and published in advance. We do not choose our endpoints after seeing which numbers look best — that is the single most common way telehealth outcome claims become marketing.

Denominators published with every number

Every reported result carries the full cohort size, the number lost to follow-up, and the number excluded — so a reader can recompute our percentages themselves.

Null and negative results published too

If a secondary endpoint shows no benefit, it is published with the same prominence as one that does. Selective reporting is disqualifying for a clinic that asks to be trusted with prescribing.

Aggregate only, never identifiable

Nothing is published below a cell size of 20 patients. No free-text, no dates of service, no geography finer than state. See our data ethics policy for the full standard.

Full governance standard: data ethics policy. Safety reporting intake: report a side effect.

Free to cite & embed

Cite this dataset

Journalists and researchers may reproduce the endpoint definitions, methodology, and any published result free of charge with attribution to Kindr Health. No permission request needed.

Citation (APA)

Kindr Health. (2026). The Kindr Outcomes Registry — real-world evidence methodology. Last verified August 1, 2026. Retrieved from https://kindr.health/outcomes

Frequently asked questions.

Why is no outcome data published yet?

Because we do not have a completed cohort. Kindr Health publishes results only after a pre-registered cohort reaches its 12-week endpoint with follow-up accounted for. Publishing anything sooner would mean publishing numbers we could not defend. This page exists so the methodology is on the record before the results are — that is what makes the results credible.

Can journalists and researchers cite this registry?

Yes. The methodology, endpoint definitions, and every published result are free to cite, quote, and republish with attribution — no permission request needed. Use the citation block on this page.

How is this different from patient reviews?

Reviews are subjective self-reported experience, published unedited. The registry is structured clinical measurement against fixed instruments. Both are published; they answer different questions and we never present one as the other.

Will negative safety findings be published?

Yes. Adverse events reported through our pharmacovigilance intake are coded continuously and reported in aggregate each quarter, including events that led patients to stop treatment.

Who reviews the registry?

The Kindr Health Clinical Team reviews the protocol, endpoint definitions, and every published report before release.

Protocol reviewed by the Kindr Health Clinical Team · NPI 1609792902 · Last reviewed August 1, 2026. Press and data enquiries: press@kindr.health · media kit

Ask Dot