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Research gaps

What we know, what's missing, and what we'd like to support.

Menopause research has covered some women well and others barely at all. Naming the gap publicly is itself a position, and an invitation.

This is where the meta-stance lives — once, not on every page. The gaps below shape what we can write about with confidence, who we can serve well, and what specific welcome hubs and pathways we've built so far in response. Race is one axis here, alongside trans women, neurodivergent readers, disabled readers, bigger bodies, and premature menopause. If you're a researcher, funder, or community organization who'd partner on closing one of these, please get in touch.

Fewer than 3% of clinical trials in conditions that disproportionately affect women are women-focused, and women-focused programme funding is concentrated in just two areas: ovarian cancer and menopause.
Lancet Obs Gyn & Women's Health, June 2026 — Women's Health Innovation Radar

What exists

The studies we lean on.

When Nila cites race, ethnicity, or sexuality differences in menopause symptoms or treatment, it's almost always coming from one of these. They're imperfect, most are U.S.-based, most are cisgender by design, and most under-sample Indigenous women, but they exist, they're peer-reviewed, and they're public.

  • SWAN (Study of Women's Health Across the Nation)

    The gold-standard longitudinal cohort, running since 1996. Oversampled Black, Hispanic, Chinese, and Japanese women. Black women enter perimenopause roughly 8.5 months earlier, have longer transitions (median 10+ years vs. 6.5 for white women), more severe vasomotor symptoms, and are less likely to be offered MHT. Hispanic women report more vaginal dryness and forgetfulness.

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  • MIDUS (Midlife in the United States)

    Longitudinal data on midlife mental and physical health, with some race and socioeconomic breakdowns. Less menopause-specific than SWAN, but useful background.

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  • PRIDE Study

    U.S. cohort of LGBTQ+ adults; has begun collecting menopause and midlife hormone data. Still small, but the only large queer-specific dataset of its kind.

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What's thin or missing

The gaps we won't pretend aren't there.

When we say "the evidence base is thin here," this is what we mean. We'd rather name the gap than write past it.

  • First Nations, Inuit, and Métis menopause

    A 2021 NCCIH scoping review found roughly thirteen peer-reviewed papers on Indigenous menopause in Canada, most small, qualitative, and community-led. Almost nothing Inuit-specific. Almost nothing Métis-specific. The medical-trauma history (residential schools, the Sixties Scoop, Inuit TB sanatorium era, Métis exclusion from coverage) shapes care-seeking at midlife in ways the literature has barely touched.

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  • LGBTQ+ midlife and menopause

    Research on lesbian and bisexual women's midlife health exists but is sparse. Trans menopause is mostly endocrine-focused, with small samples. The Endocrine Society's 2017 trans guidelines acknowledge menopause data is "essentially absent."

  • Trans women on long-term estrogen

    There is almost no longitudinal data on what happens to trans women if exogenous estrogen drops, is interrupted, or is reduced in midlife. The symptom picture (vasomotor, sleep, mood, bone) is biologically plausible from cis-menopause physiology, but the trials don't exist. We write about it on the trans-women hub because the silence isn't neutral, but we mark it as low-grade evidence on purpose.

  • Bigger bodies and menopause

    Body size changes risk profiles (cardiometabolic, breast cancer, fracture, MHT dosing) in ways that matter clinically. Most trials either excluded higher-BMI participants or didn't stratify by them, and weight-stigma in clinical settings means symptoms get attributed to size rather than hormones. The honest picture for women in larger bodies is patchier than the textbook suggests.

  • Premature and early menopause

    Premature ovarian insufficiency (before 40) and early menopause (40–45) are studied as endocrine events, but the long-arc questions, what does forty years of post-menopause look like for bone, brain and heart, and how should MHT be dosed across that span, sit on much thinner data than the average-age cohorts.

  • Surgical menopause care and counselling

    There is almost no large-scale evidence on what women are actually told before an oophorectomy or how well surgical menopause is managed afterwards. The best current snapshot is Menopause Support's 2024 patient survey of 521 women in surgical menopause: 74.5% said they were not told about potential side effects of removing their ovaries, and most reported no menopause-trained follow-up. Patient-org data, not a peer-reviewed cohort — but it's currently the most cited number we have, which is itself a gap.

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  • Menopause training in medical schools

    Menopause Support's FOI-based survey of UK medical schools showed extreme variation in how much (and whether) menopause is taught at undergraduate level — from a few hours to essentially nothing. Mandatory menopause teaching was committed to from 2024 onwards, but the back-catalogue of qualified doctors trained without it is the cohort most patients are still meeting. There is no equivalent published audit for Canadian or US medical schools that we've found.

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  • Neurodivergent women through perimenopause

    ADHD and autism research in adult women is itself recent. The intersection with perimenopause (estrogen's effect on dopamine, late diagnosis at midlife, executive-function collapse during the transition) is almost entirely clinical observation and lived-experience writing, with primary research only just starting.

  • Disability and menopause

    A 2023 BMJ scoping review concluded the field is "in its infancy." Almost no work on how chronic illness, mobility limitation, or sensory disability intersects with the menopause transition or treatment access.

  • Intersectional symptom and access data

    Even SWAN doesn't break out Black + queer, Indigenous + disabled, racialized + neurodivergent. Treatment access disparities by race and sexuality together, not just one axis, are largely anecdotal.

  • Sex and gender treated as one field

    Most menopause research, and most clinical intake forms, collapse sex-at-birth and gender identity into a single "female" checkbox. That erases trans women on estrogen, trans men post-oophorectomy, non-binary people on HRT, and intersex people whose hormone-and-symptom picture maps onto menopause physiology. It also makes it impossible to tell, after the fact, who a study's findings actually apply to. The physiology is what drives symptoms and treatment; the identity is what shapes access and how symptoms get heard. Both matter, and they need separate fields.

  • Menopause stage and cause, standardized

    STRAW+10 (the Stages of Reproductive Aging Workshop) is the closest thing to a shared vocabulary for perimenopause, menopause, and postmenopause, and it's barely used outside academic papers. Cause of menopause — natural, surgical, medical/chemo, iatrogenic, POI, gender-affirming — is even patchier. When those categories aren't captured consistently, surgical menopause and POI keep getting folded into "postmenopausal women" in trials, and the lived reality (younger onset, abrupter drop, longer treatment horizon) disappears into the average.

  • Symptom scales built on a narrow sample

    The Menopause Rating Scale, the Greene Climacteric Scale, and MENQoL are the questionnaires most doctors and researchers reach for. They were built and validated on largely white, cisgender, neurotypical cohorts in their early 50s. They under-weight the symptoms readers tell us matter most (executive function, sensory overwhelm, joint and muscle pain, GSM), and they don't translate cleanly for people whose menopause was surgical, medical, early, or on exogenous hormones. Useful, but not the whole picture.

  • Cycle and symptom data locked in consumer apps

    Most people entering perimenopause already have years of cycle and symptom data in a tracker app. Almost none of it moves cleanly to a clinician, a specialist, or another app. The absence of a shared export format means the person with the longest, richest record of their own transition can't easily hand it over when they finally get an appointment. Data portability is a menopause-care issue, not just a privacy one.

Open calls you can back right now

Small, fundable studies looking for readers, not just institutions.

Curated, editorial only. We list live crowdfunds and recruitment calls where the study directly addresses one of the gaps above and the money moves through a legitimate research host (a university, registered charity, or established grant body). We take no fee, no cut, no affiliate link. If you know of a study that fits, or a reader-supported recruitment call, tell us.

  • LiveMedical Research Foundation · mref.uk

    CST-Meno: adapting Cognitive Stimulation Therapy for menopause-related brain fog

    Crowdfund via the Medical Research Foundation (UK). A team is adapting an evidence-based dementia protocol, Cognitive Stimulation Therapy, to test whether it also helps the word-finding, focus and processing-speed changes women describe in perimenopause.

    Important caveat we want up front: menopausal brain fog is not early dementia — the whole point of studying CST here is that a protocol proven to help cognition in one context might help another, not that the two conditions are the same. Menopause brain-fog research is chronically underfunded, and small consumer-backed grants like this are one of the few ways non-pharma cognitive interventions get tested at all. Nila is collaborating with the team on parts of this work and has the founder's go-ahead to share it here.

    Editorial disclosure: Nila is collaborating with the project team. No money or in-kind value flows to Nila from listing this.

    Back this study

What we'd partner on

Three shapes this could take.

None of these are commitments yet. They're the projects we'd say yes to if the right partner, a community organization, a funder, a research team, came to the table.

01

Curated long-read

A Premium piece pulling SWAN, the NCCIH scoping review, PRIDE, and Indigenous-led work into one place. Mostly reading and citation work. Six weeks.

02

Community-led primary research

A survey or mixed-methods study with a partner organization, for example Rainbow Health Ontario, the Native Women's Association of Canada, or a disability-justice group. Real ethics review, real budget, real timeline (12–18 months).

03

Lived-experience archive

An opt-in member story project, tagged by identity, surfaced respectfully. Lower scientific rigour than primary research, but high value, and Nila is uniquely placed to host it because the audience is already here.

Signals the field is shifting

The gap is starting to be named by people who can move money.

None of this fixes the back-catalogue. But the last twenty-four months have brought the biggest real-world evidence study women's health has ever had, a serious WEF mapping of the science-to-patient gap, and close to half a billion dollars of new philanthropic commitment. Worth naming, because the silence used to be the story.

  • Ozmen et al. (2026) — Surgical menopause and GSM severity

    First sizeable comparison of genitourinary syndrome of menopause (GSM) burden in surgical vs natural menopause, published in Menopause (journal of The Menopause Society). Surgical menopause came with significantly more severe GSM exam findings and symptoms (dryness, painful sex, reduced desire, dysuria, urinary frequency), adjusted OR 1.08 per point of severity (95% CI 1.04–1.12). Matters because surgical-menopause patients have historically been folded into 'postmenopausal women' in trials; the field is finally treating them as their own population, which is what the lived experience has been saying for years.

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  • Apple Women's Health Study (Harvard Chan / Apple / NIEHS)

    The first long-term, at-scale study pairing iPhone and Apple Watch cycle data with periodic surveys to map menstrual patterns against gynecologic and broader health outcomes — including perimenopause and menopause. Real-world evidence at a scale the classic cohorts (SWAN, MIDUS) could never reach. iOS 26 also added menopause and perimenopause life-stage tracking in the Health app, which feeds back into this work. Credit: Harvard T.H. Chan School of Public Health, Apple Inc., and NIEHS.

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  • WEF Women's Health Innovation Radar (2025)

    World Economic Forum mapping of where women's-health innovation is concentrated and where the science-to-patient pipeline breaks down. Names menopause as one of the high-impact conditions where translation, not just discovery, is the bottleneck. Useful framing for why a consumer platform like Nila exists alongside the labs.

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  • Wellcome Leap + Pivotal Life Sciences — US$250M women's-health commitment

    Wellcome Leap's partnership with Pivotal Life Sciences puts a quarter of a billion dollars behind women's-health research programs. Not menopause-exclusive, but the scale signals the funding gap is finally being named by people who can move money.

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  • Melinda French Gates — US$215M for women's health worldwide

    Pivotal Ventures' 2024 commitment to improving women's health globally, with a stated focus on under-studied conditions and historically excluded populations. Same direction of travel as the Wellcome Leap announcement: the philanthropy capital is starting to land where the evidence base is thinnest.

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  • Kearney [w]Health Employer Index 2026

    Annual benchmark of how employers cover women's health — including menopause — in benefits design. The 2026 report frames the shift from awareness to accountability, which matters because workplace coverage is one of the few levers that closes the access gap quickly while the trials catch up.

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  • Menopause Mandate Mega Menopause Survey 2025 / MM25

    A UK patient survey completed by more than 15,000 women, with UCL research support. It surfaces the honest reality of menopause support today: what has improved, what is still missing, and where urgent change is needed — from access to informed medical care to which employers are stepping up. Patient-org data at a scale most clinical cohorts don't reach, and a useful counterweight to employer self-reported benchmarks.

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  • SOGC / Medscape Canada — Lack of menopause care reflects systemic issues (July 2026)

    The Society of Obstetricians and Gynaecologists of Canada names publicly what patients have been saying for years: primary-care menopause training isn't mandatory, fee-for-service under-pays counselling, and there's no billing code for group or novel care models. The 2002 WHI overcorrection scared a whole generation of prescribers away from MHT, and the gap is now being filled by private clinics charging $500+ a visit with uneven oversight. Bill S-243, a national framework for women's health in Canada, is currently moving through the Senate. Worth flagging alongside the funding signals above: the gap is being named by the professional body, not just patients.

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Researcher, funder, or community organization with a stake in this? We'd love to hear from you.