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.
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.
SourceMIDUS (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.
SourcePRIDE 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.
Source
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.
Perimenopause itself, compared with menopause
A 2026 analysis in Menopause by Mary Hedges and colleagues (Mayo Clinic and Flo Health) counted the literature and found perimenopause studied far less than postmenopause — despite being the stage where symptoms usually start and where most people first ask for help. If your perimenopause questions come back vague, part of the reason is structural.
SourceThe records the research is built on
A September 2026 scoping review in Menopause found that menopause status and symptoms are recorded inconsistently in electronic health records. Stage is usually inferred from proxies like age band, a diagnosis code or a prescription rather than written down, and symptom detail sits in free-text notes instead of structured fields. That means care doesn't travel well between providers, and researchers can't reliably compare one population with another. The authors call for standardized menopause data elements and validated symptom tools built into the record itself. Many of the gaps below start here.
SourceThe funding line underneath all of this
The National Academies' consensus report on women's health research puts women's-health research at roughly 7.9% of NIH funding, a share that has stayed broadly flat while the overall budget grew. Every gap on this page sits downstream of that number.
SourceDrug doses, across the cycle and after menopause
Estrogen changes how the body absorbs, metabolises and clears a lot of medication, through gut transit, body composition, CYP450 and UGT enzymes, and P-glycoprotein transport. A 2025 review in Expert Opinion on Drug Metabolism & Toxicology pulls that evidence together and notes women report adverse drug reactions about twice as often as men. A separate 2025 meta-analysis found blood levels of some antiseizure medications and lithium move measurably between the follicular and luteal phase, with bigger swings in people whose seizures track their cycle. Very little of this reaches dosing guidance, and almost none of it is followed through the menopause transition itself, when estrogen is changing week to week.
SourceFirst 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.
SourceLGBTQ+ 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.
SourceMenopause 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.
SourceNeurodivergent 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.
What we're trying so far
The welcome hubs and pathways built in response.
None of these close the gap. They're our honest first move while the literature catches up — written carefully where the evidence supports it, quiet where it doesn't, and openly inviting paid contributors from each community to shape what comes next.
Umbrella pathway
Women of colour & midlife
Multi-group, evidence-led: SWAN on vasomotor variation, FRAX caveats, dermatology gaps, practitioner concordance.
ReadNamed hub
Black women & midlife
Where we currently hold the most evidence (SWAN, fibroids, MHT access) and are furthest along commissioning paid Black contributors.
ReadNamed hub
Trans women & midlife
Anchored on estrogen-drop physiology in trans women, marked as low-grade evidence on purpose.
ReadNamed hub
Neurodivergent & midlife
ADHD, autism and late-diagnosis-at-midlife through perimenopause, with lived-experience writing where the research is thinnest.
ReadNamed hub
Gender & midlife
The gendered script around menopause: who gets believed, who gets MHT, whose symptoms get attributed to age or mood instead.
ReadUmbrella doorway
Who this is for
Ten lived-moment doorways into the site, including premature menopause, bigger bodies, disability, and sole carers.
Read
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.
JAMA Medical News (July 2026) — "Wild West or Gold Rush": the menopause marketplace, examined
A JAMA news feature on what happened after decades of neglect: a boom in products, telehealth and influencer advice that now outpaces the evidence behind it. The numbers in it are the part worth keeping. A Mayo Clinic analysis led by Stephanie Faubion found menopausal hormone therapy use in the US had fallen to 1.7% by 2023, against nearly 1 in 4 women before the 2002 WHI fallout — so the treatment with the strongest evidence is still the least used, while less-studied options fill the space. Nanette Santoro's line on testosterone being at "an all-time fever pitch", Faubion calling stacks of hormone-level printouts "close to worthless" because levels swing day to day, and Raffael Heiss's work on parasocial trust in influencers all land in the same place: interest has run ahead of research. Also flags a companion JAMA Network Open study finding people describe emotional and cognitive symptoms far more often in online forums than they appear in their own medical records.
SourceCanino et al. (2026) — Twenty-five years of supplement research, counted
A bibliometric analysis in Menopause mapped every US dietary-supplement intervention study on menopause from 2000–2024. The whole literature comes to 253 publications, growing at 3.89% a year, spread thin across more than 80 different ingredients — and 234 of those studies look at postmenopause. Perimenopause, the stage where most people start reaching for supplements, is almost absent. That combination (many ingredients, few studies each, almost no replication) is exactly why so much of our supplement shelf grades low: it isn't that the products failed, it's that the research was never done.
SourceGreenShield + Women's Health Collective Canada — first national Canadian menopause study (August 2026)
A major Canadian insurer and a women's-health philanthropy are jointly funding Can-RISE, the first national investigator-led study of perimenopause, menopause and post-menopause in Canada. It explicitly centres equity-deserving populations and the health, social and economic effects of the transition — including at work. The fact that this data didn't exist at a national level until now is itself the gap.
SourceManulife Canada (2025) — HRT claims up 228% in five years
Manulife's aggregate claims data shows hormone therapy claims among Canadian women aged 45–54 rose 228% from 2021 to 2025 — one of the first insurer-level confirmations that Canadian demand is finally climbing after two decades of the WHI chill, in the same age band as Canada's average menopause age of 52. It's a claims-based figure (employed women with benefits), so it undercounts the uninsured and anyone paying out of pocket, but it tracks with what pharmacists and clinics report on the ground. Demand moving is not the same as the evidence gap closing — but it's the demand-side signal the research pipeline has been waiting for. Source: Manulife Canada aggregate claims data, 2021–2025, cited in a Manulife/Cleveland Clinic Canada article.
SourceNHS Business Services Authority / The Pharmaceutical Journal (2026) — who England's HRT rise reached
England's HRT prescribing more than doubled since 2020/21, from 781,170 women aged 40 and over to 2,038,025. The deprivation gap held anyway: about 8.8 in every 100 women over 40 in the most deprived fifth of England receive HRT, against 14.2 in 100 everywhere else, with Newham at 4.5 per 100 and Brighton and Hove at 23.4. A Menopause All-Party Parliamentary Group report found Black women five times less likely to be prescribed HRT than White women (5.2% vs 23.3%) and Asian women four times less likely (6.2%). Pharmacists interviewed name appointment access, clinician confidence, translator availability, faith and cultural attitudes, and a breast cancer message from 2002 that is still doing quiet work. One caution worth keeping: a low prescribing rate is not proof of unmet need on its own, which is exactly why symptom data has to be collected separately from prescribing data. Canada has no equivalent national figures, which is its own gap.
SourceAPPG on Menopause / Wellbeing of Women (October 2025) — Rebuilding trust: tackling inequity in menopause care
A UK parliamentary inquiry that asked who menopause care is failing, and heard from six groups in turn. Disabled and neurodivergent women, whose symptoms get filed under their existing condition. Ethnic minority communities, where Black women are five times and Asian women four times less likely to be prescribed HRT than White women, and earlier onset ages go unrecognised. LGBTQIA+ people, excluded by the language of the services themselves, with the 2024 NICE guideline silent on anyone taking gender-affirming hormone therapy. People in poverty, blocked by ID and fixed-address rules and digital-only booking. Domestic abuse survivors, who receive trauma-uninformed care, whose perimenopause is associated with starting around 35% earlier, and two thirds of whom report abuse increasing during menopause. And women in prison, a group that grew 179.5% among those 50 and over between 2003 and 2023, facing convoluted medication access and almost no privacy. The recurring shape matters more than any single figure: no tailored information, then stigma and silence, then late help-seeking, into a setting that was not built for them. The inquiry's own conclusion is a research gap, and its fifth recommendation is dedicated funding to close it.
SourceOzmen 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.
SourceApple 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.
SourceWEF 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.
SourceWellcome 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.
SourceMelinda 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.
SourceKearney [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.
SourceMenopause 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.
SourceSOGC / 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.
Source
Researcher, funder, or community organization with a stake in this? We'd love to hear from you.

