This article estimates the prevalence and identifies risk factors of resident aggression and abuse in assisted living facilities. 1 key finding →
Evidence: low
Full summary, score breakdown and related studies → Original source
30,580 Alzheimer's and dementia studies in plain English, each scored out of 100.
This article estimates the prevalence and identifies risk factors of resident aggression and abuse in assisted living facilities. 1 key finding →
Evidence: low
Full summary, score breakdown and related studies → Original source
Interprofessional collaboration (IPC) is essential for high-quality palliative care (PC) for persons with dementia. 2 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
LGBTQ + older adults have a high likelihood of accessing nursing home care. 4 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Older age and comorbid conditions increase risk for severe for respiratory syncytial virus (RSV). 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
There were 1673 teleconsultations conducted with 850 unique patients. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
This article describes and illustrates a framework that may be used when assessing the moral basis of everyday issues that can affect residents of assisted living facilities. 4 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
The increasing elderly population is driving higher utilization rates of long-term care facilities, where residents often have multiple chronic diseases, making them potential candidates for palliative care. 2 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Although much of the research on service use by older adults with dementia relies on proxy reports by informal caregivers, little research assesses the accuracy of these reports, and that which does exist, does not focus on home care services. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Training gaps in the U.S. dementia care workforce impact patient support. 3 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Dementia is one of the leading causes of death in the US. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
The care of a patient with neurologic disease at end-of-life requires expertise in addressing advance care planning, hospice, symptom management, and caregiver support. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Recent policy focus in dementia care has been on living well with the condition; however, being able to die well with dementia is of equal importance. 4 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Of 3883 older adults receiving a first palliative care consultation from this organization, 22% (855) had a dementia diagnosis. 5 key findings →
Evidence: moderate
Full summary, score breakdown and related studies → Original source
Advance care planning (ACP) in palliative care is essential for patient autonomy and quality of dying. 1 key finding →
Evidence: low
Full summary, score breakdown and related studies → Original source
Dementia is characterised by memory loss, behavioural changes and decline of cognitive, social and physical functions and is a life-limiting condition. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Dementia usually occurs as a result of brain disease and, while it is usually chronic or progressive in nature, it has not traditionally been conceptualised as a terminal or life-limiting syndrome. 1 key finding →
Evidence: low
Full summary, score breakdown and related studies → Original source
Fifty respondents identified themselves as music therapists currently working with clients receiving PEOLC. 4 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Individuals from minoritized racial/ethnic groups face a disproportionate burden of Alzheimer's disease and related dementias. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
The burden of neurological disease is increasing globally. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Older adults classified with dementia were more likely to drop out of the labor force and become poor than similar older adults without dementia. 3 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Dementia is a major health concern in society, particularly in the aging population. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
During follow up (mean 11.1 years), 13% of Veterans developed dementia. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Compared to White participants, Black, Hispanic, and Asian participants reported taking fewer total medications (incidence rate ratio [IRR] ± standard error[SE] = 0.903 ± 0.017, 0.875 ± 0.021, and 0.912 ± 0.041, respectively, all p < 0.01). 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
The Washington University School of Medicine Knight Alzheimer Disease Research Center's "African American Participation in Alzheimer Disease Research: Effective Strategies" Workshop convened to address a major limitation of the ongoing scientific progress regarding Alzheimer's disease and related dementias (ADRD): participants in most ADRD research programs overwhelmingly have been limited to non-Hispanic white persons, thus precluding knowledge as to how ADRD may be represented in non-white individuals. 2 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Significant disparities in symptom severity reported by Alzheimer's caretakers were observed among the racial groups analyzed. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Free full text links and the Full text may need a subscription label come from Unpaywall, Europe PMC and OpenAlex records of free copies, checked 10 Oct 2026. A study with neither is unknown, not paywalled. Show only studies that are free to read
This is alzhub's own score. It is not an official metric, not an impact factor, and no journal, publisher or ranking body endorses it. We built it so that a reader who is not a scientist can tell a landmark trial from a conference abstract without having to already know the difference. Every point comes from one of 20 components, all of them printed on the study itself, so you can disagree with our arithmetic rather than having to trust the total.
Journals are placed in ordered tiers, never given a numeric impact factor — we could not verify current impact factors from a source we control, and an invented one would be worse than none. Tier 1 is the top-tier general journals (NEJM, The Lancet, JAMA, Nature, Science, Nature Medicine); tier 2 is the leading specialty journals; tier 3 is every other peer-reviewed journal. A separate part scores how much the journal's own papers are cited, which tells the tier-3 journals apart.
Two rules we don't bend. First, we never fill in a missing value: if a record does not state a sample size or a design, that component scores zero, and if we simply have no data for a part, such as a citation count, that part is left out and the study is scored on the parts we could check. The study card says which. Second, anything that is not a peer-reviewed article is capped at 16/100 and carries a warning chip — so a conference abstract or a company press release can never outrank a peer-reviewed paper, no matter how good it looks.
We rank a rigorous null result — a good trial showing that something does not work — above an early positive finding. Someone deciding whether to buy a supplement is served by that, and the rigour is already counted by the design and journal components.
The score is computed from the published data alone and is reproducible: the same file always yields the same numbers.
See the whole rubric drawn out → — four charts covering all 30,580 studies: how the scores are spread and where the cap bites, which of the 20 components the library is strong and weak on, which subjects rest on stronger evidence, and what kinds of study each subject is actually built from.
This is a large sample of the Alzheimer's literature, not an exhaustive index of it. It holds 30,580 records, built mostly from automated pulls of Europe PMC (64.7% of the library) and OpenAlex (16.6%), plus smaller pulls from PubMed, Crossref and medRxiv. If a study, a drug, or a finding isn't here, that is not evidence it doesn't exist in the literature — it may simply not have been pulled in yet.
1,037 records (3.4% of the library) are not peer-reviewed — 964 of those are preprints posted before any journal review, and the rest are conference abstracts, regulatory notices and reports. Every study card on this page states its status plainly, and the score above is capped for anything that isn't a peer-reviewed article.
See the full, machine-readable breakdown of this library's coverage →
Newest studies, as a dated timeline → Atom feed Where this research is being discussed: events