Get help now — free helplines

You can call any of these for free. You do not need a diagnosis, an appointment, or a crisis to call — questions and plain exhaustion are reasons enough.

  • Alzheimer's Association 24/7 Helpline 800-272-3900 24 hours a day, 365 days a year Free, confidential support and information for people with dementia, caregivers, families and the public. Master's-level clinicians. Also Spanish.
  • 988 Suicide & Crisis Lifeline 988 24/7 Call or text 988, or chat at 988lifeline.org. For anyone in emotional distress or a mental-health crisis, including caregivers.
  • Alzheimer's Foundation of America (AFA) Helpline 866-232-8484 9:00 am - 9:00 pm ET, seven days a week Licensed social workers providing support, info and referrals. Also text message and web chat. Text: 646-586-5283

In a medical emergency, call 911. More numbers, and what each line does, on the help page.

This page is alzhub.org's plain-English summary of a published study, not the paper itself. It is generated from the record we hold for this study, sourced and linked below — check the original for the full text and methods.

⚠ Preprint — not yet peer-reviewed alzhub usefulness score 16 out of 100. Treatments

Topic: Health services, long-term care and technology

Simulation-based validation demonstrates the framework’s analytical capability. Under calibrated coefficients, the nine-attribute design achieves a D-error of 0.0023, adequate for mixed logit estimation with preference heterogeneity. Key illustrative findings include: (a) implementation-related attributes collectively account for 42.5% of total preference importance, exceeding treatment characteristics alone (35.9%); (b) geographic access to treatment centres and diagnostic pathway choice are the most highly valued implementation factors (WTP: EUR 20,571 and EUR 18,571 per year, respectively); (c) latent class analysis identifies three distinct preference segments (efficacy-driven, access-prioritising, and risk-averse) with implications for patient-centred implementation. The framework is designed for adaptation to different European contexts through country-specific level calibration: for example, cost levels calibrated to national pharmaceutical pricing, travel distances calibrated to geographic dispersion of specialist centres, and waiting times calibrated to local healthcare system capacity. PREFER-DMT provides a standardised, validated, and immediately deployable DCE framework for multi-country preference elicitation on Alzheimer’s DMT implementation in Europe. By covering implementation factors alongside treatment characteristics, the framework generates evidence directly relevant to the system-level decisions that European HTA bodies must make. The framework is operationalised as an open-access interactive platform and is available for adoption by national DMT working groups, HTA agencies, and research consortia.

Key findings

Study details

How this study scored 16/100
How this study's score is builtJournal tier 2 of 10; Journal's citation record 0 of 4; Study design 12 of 12; Strength of evidence 5 of 5; Peer-review validation 4 of 10; How recent 5 of 5; Sample size 0 of 4; Effect reported 2 of 3; Studied in people 0 of 3; Randomised / blinded 0 of 2; Times cited left out, no data; Citations per year left out, no data; Impact for its field and year left out, no data; Cited by studies here left out, no data; Still being cited left out, no data; Senior author's track record left out, no data; Institution's track record left out, no data; Multi-centre collaboration left out, no data; Indexed in PubMed 1 of 2; Free to read 0 of 2. 31 of the 62 points it could be judged on, which is 50 of 100. Raw total 50 of 100, shown as 16 because this is not a peer-reviewed research article.raw total 50 of 100capped at 16 — hatched points do not count

Preprint — not yet peer-reviewed. It scored 50 on the same rubric, but non-peer-reviewed sources are capped at 16, so it shows as 16. Scored zero for sample size and studied in people because the record does not state it. We have no data on times cited, citations per year, impact for its field and year, cited by studies here, still being cited, senior author's track record, institution's track record and multi-centre collaboration, so those were left out: it earned 31 of the 62 points we could judge it on, which is 50 out of 100.

ComponentPointsWhy
Journal tier 2 / 10 Tier 4 — not a peer-reviewed journal (Research Square)
Journal's citation record 0 / 4 Not a journal article, so the journal's record does not count
Study design 12 / 12 A systematic review of all the studies on the question
Strength of evidence 5 / 5 Rated “high” in our summary
Peer-review validation 4 / 10 Preprint — not yet peer-reviewed. Hosted on a preprint server.
How recent 5 / 5 2026 — within 1 year(s) of the newest study here
Sample size 0 / 4 Participant count not stated — scores zero (not stated in the record — scored 0)
Effect reported 2 / 3 Effect reported as a number, without an interval or test
Studied in people 0 / 3 Not stated whether this was studied in people — scores zero (not stated in the record — scored 0)
Randomised / blinded 0 / 2 A review of other studies — randomisation is not credited here
Times cited — / 7 No citation count (not found in OpenAlex) — left out of this score
Citations per year — / 5 No citation count or no year — left out of this score
Impact for its field and year — / 6 No field-weighted citation impact (OpenAlex has none yet) — left out of this score
Cited by studies here — / 6 Not yet checked against this library's citation graph — left out of this score
Still being cited — / 4 No yearly citation counts — left out of this score
Senior author's track record — / 4 Senior author's record not available — left out of this score
Institution's track record — / 3 No institution listed in OpenAlex — left out of this score
Multi-centre collaboration — / 3 Institutions not listed — left out of this score
Indexed in PubMed 1 / 2 Not in PubMed, but has a DOI
Free to read 0 / 2 Behind a paywall — scores zero
Points 31 / 62 Scored on 12 of 20 parts. We have no data for the rest, so they are left out: 31 of the 62 points we could judge it on is 50 out of 100.
Total 50 / 100 Capped to 16 because this is not a peer-reviewed article.

What each of these 20 components measures, and what this score is not →

Read the original

Free copy unknown: no free-copy check has an answer for this record yet. That does not mean it is paywalled.

Cite this study APA, Vancouver, BibTeX · download .bib or .ris

Built from the record alzhub holds for this paper, not looked up. Volume, issue and page numbers are not held in the record. Check the citation against the original before you use it.

APA 7th

Sen, S. E. (2026). PREFER-DMT: A Discrete Choice Experiment Framework for Eliciting Stakeholder Preferences on Disease-Modifying Therapy Implementation in European Healthcare Systems. Research Square. https://doi.org/10.21203/rs.3.rs-9405777/v1

Vancouver

Sen SE. PREFER-DMT: A Discrete Choice Experiment Framework for Eliciting Stakeholder Preferences on Disease-Modifying Therapy Implementation in European Healthcare Systems. Research Square. 2026. doi:10.21203/rs.3.rs-9405777/v1.

BibTeX

@article{sen2026-17588c9d,
  author  = {Sen, S. E.},
  title   = {{PREFER-DMT: A Discrete Choice Experiment Framework for Eliciting Stakeholder Preferences on Disease-Modifying Therapy Implementation in European Healthcare Systems}},
  journal = {Research Square},
  year    = {2026},
  doi     = {10.21203/rs.3.rs-9405777/v1},
  url     = {https://doi.org/10.21203/rs.3.rs-9405777/v1}
}

Related studies in Treatments

Similar studies

More on Treatments

See all studies in Treatments →