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Sharing patient technology preferences with care networks: Stakeholders’ views of the “Let’s Talk Tech” decision aid for dementia care
Clara W. Berridge, Natalie R. Turner, William B. Lober, George Demiris, JEFFREY A. KAYE. Journal of Alzheimer s Disease, 2025-05-01
Topic: Risk, prevention and care in population studies
BackgroundLet's Talk Tech (LTT) is a self-administered web intervention for people with memory loss and their care partners that supports decision-making about digital health technologies. In past work, dyads wanted to share LTT preference reports with their larger care networks.ObjectiveThis study aims to understand with whom care dyads want to share their technology preference reports and why, and if and how clinicians want to receive them.MethodsTogether, fifteen dyads of people living with mild cognitive impairment (MCI) or early-stage dementia (n = 15) and a care partner (n = 15) completed LTT and two survey questions. Care partners completed independent follow-up interviews, and 32 clinicians at four Alzheimer's Disease Research Center-affiliated clinics viewed an LTT report and completed a 10-question survey. We used descriptive statistics for survey responses and thematic analysis for interviews.ResultsTwo-thirds of care partners (n = 10) wanted to share the report with family members. Half (n = 8) wanted to share it with clinicians to keep them informed about the dyad's planning and facilitate conversations about technology options. 30 of 32 clinicians reported they would want their patients' technology preferences reports, with 25 wanting to access it via the electronic health record (EHR).ConclusionsFindings demonstrate potential value to both family dyads and providers of sharing technology preferences beyond the care dyad. Clinicians were highly receptive to accessing technology preference reports in EHRs and to having discussions about technology be a part of advance care planning. Future research should test integration in the EHR and the potential of sharing technology preferences to support person-centered technology choices.
Key findings
- Care partners completed independent follow-up interviews, and 32 clinicians at four Alzheimer's Disease Research Center-affiliated clinics viewed an LTT report and completed a 10-question survey.
- We used descriptive statistics for survey responses and thematic analysis for interviews.ResultsTwo-thirds of care partners (n = 10) wanted to share the report with family members.
- Half (n = 8) wanted to share it with clinicians to keep them informed about the dyad's planning and facilitate conversations about technology options. 30 of 32 clinicians reported they would want their patients' technology preferences reports, with 25 wanting to access it via the electronic health record (EHR).ConclusionsFindings demonstrate potential value to both family dyads and providers of sharing technology preferences beyond the care dyad.
- Clinicians were highly receptive to accessing technology preference reports in EHRs and to having discussions about technology be a part of advance care planning.
- Future research should test integration in the EHR and the potential of sharing technology preferences to support person-centered technology choices.
Why it matters
In this study, most care partners wanted to share technology preference reports with family and clinicians, and 30 of 32 clinicians said they would want such reports. It concerns sharing preferences about digital health technologies, not treating or preventing Alzheimer's disease.
Study details
- Participants15
- Evidence strengthLow
How this study scored 47/100
Published in a peer-reviewed journal. Scored zero for study design, effect reported and randomised / blinded because the record does not state it.
| Component | Points | Why |
|---|---|---|
| Journal tier | 7 / 10 | Tier 3 — peer-reviewed journal (Journal of Alzheimer s Disease) |
| Journal's citation record | 2 / 4 | Journal of Alzheimer s Disease: journal h-index 218 (OpenAlex, 2026-10-29) |
| Study design | 0 / 12 | No study design recorded — scores zero, not guessed (not stated in the record — scored 0) |
| Strength of evidence | 1 / 5 | Rated “low” in our summary |
| Peer-review validation | 10 / 10 | Peer-reviewed. Published as an article in a named peer-reviewed journal. |
| How recent | 4 / 5 | 2025 — within 3 year(s) of the newest study here |
| Sample size | 1 / 4 | 15 participants |
| Effect reported | 0 / 3 | No effect size reported — scores zero (not stated in the record — scored 0) |
| Studied in people | 3 / 3 | Studied in people (participant count stated) |
| Randomised / blinded | 0 / 2 | No randomisation or blinding stated — scores zero (not stated in the record — scored 0) |
| Times cited | 1 / 7 | Cited 3 times (OpenAlex, 2026-10-10) |
| Citations per year | 1 / 5 | 1.0 citations a year over 3 year(s) since 2025 |
| Impact for its field and year | 3 / 6 | Cited 7.0× the average for papers of its field and year (OpenAlex FWCI) |
| Cited by studies here | 1 / 6 | Cited by 1 other studies in this library |
| Still being cited | 1 / 4 | Cited 3 times in 2024–2026 (2026 still in progress; OpenAlex) |
| Senior author's track record | 4 / 4 | Last-listed author Jeffrey Alan Kaye: h-index 122 (OpenAlex, whole career) |
| Institution's track record | 3 / 3 | University of Washington: institution h-index 3,540 (OpenAlex) |
| Multi-centre collaboration | 1 / 3 | OpenAlex lists 3 institution(s) in 1 country |
| Indexed in PubMed | 2 / 2 | Indexed in PubMed (PMID 40313054) |
| Free to read | 2 / 2 | Free to read |
| Total | 47 / 100 | — |
What each of these 20 components measures, and what this score is not →
Read the original
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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
Berridge, C. W., Turner, N. R., Lober, W. B., Demiris, G., & JEFFREY A., K. A. Y. E. (2025). Sharing patient technology preferences with care networks: Stakeholders’ views of the “Let’s Talk Tech” decision aid for dementia care. Journal of Alzheimer s Disease. https://doi.org/10.1177/13872877251332659
Vancouver
Berridge CW, Turner NR, Lober WB, Demiris G, JEFFREY A. KAYE. Sharing patient technology preferences with care networks: Stakeholders’ views of the “Let’s Talk Tech” decision aid for dementia care. Journal of Alzheimer s Disease. 2025. doi:10.1177/13872877251332659. PMID: 40313054.
BibTeX
@article{berridge2025-40313054,
author = {Berridge, Clara W. and Turner, Natalie R. and Lober, William B. and Demiris, George and JEFFREY A., K. A. Y. E.},
title = {{Sharing patient technology preferences with care networks: Stakeholders’ views of the “Let’s Talk Tech” decision aid for dementia care}},
journal = {Journal of Alzheimer s Disease},
year = {2025},
doi = {10.1177/13872877251332659},
pmid = {40313054},
url = {https://doi.org/10.1177/13872877251332659}
}
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