ArticleJournal of medical Internet research2018
Scaling PatientsLikeMe via a "Generalized Platform" for Members with Chronic Illness: Web-Based Survey Study of Benefits Arising.
Article in Journal of medical Internet research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
25 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.
- Digital Patient Experience: Umbrella Systematic Review.Journal of medical Internet research · 2022Pooled it
- Therapeutic Patient Education in the Digital Era: Opportunities and Challenges in Diabetes Care.Mayo Clinic proceedings. Digital health · 2025Review
- Transformative Impact of the Internet on the Boundaries for the Physician Profession: Why Materiality Matters.Journal of medical Internet research · 2025Article
- Companionship and Sharing Create Social Connections of an Online Community-Based Intervention for Patients with Cancer Receiving Outpatient Care: Pilot Study.JMIR cancer · 2025Article
- Evaluating the User-Perceived Benefit of a Virtual Lung Cancer Patient Education and Support Community: LVNG With Lung Cancer.Journal of the advanced practitioner in oncology · 2024Article
- PatientsLikeMe and Online Patient Support Communities in Dermatology.JMIR dermatology · 2024Article
- Online peer support for people with Amyotrophic Lateral Sclerosis (ALS): a narrative synthesis systematic review.Frontiers in digital health · 2024Review
- Role Preferences in Medical Decision Making: Relevance and Implications for Health Preference Research.The patient · 2024Article
- Associations Between Patient-Reported Outcome Measures of Physical and Psychological Functioning and Willingness to Share Social Media Data for Research Among Adolescents With a Chronic Rheumatic Disease: Cross-Sectional Survey.JMIR pediatrics and parenting · 2023Article
- Online Health Communities: an alternative feasible data registry tool for developing countries.Health research policy and systems · 2023Article
- Malthusian Trajectory for Heart Failure and Novel Translational Ambulatory Technologies.Current cardiology reviews · 2023Review
- Development of dynamic health care delivery heatmaps for end-of-life cancer care: a cohort study.BMJ open · 2022Article
- The use of Big Data Analytics in healthcare.Journal of big data · 2022Article
- Audience of Academic Otolaryngology on Twitter: Cross-sectional Study.JMIR medical education · 2021Article
- Behavioral Theory-Based Framework for Prediabetes Self-Care System-Design Perspectives and Validation Results.International journal of environmental research and public health · 2021Article
- Leveraging innovative technology to generate drug response phenotypes for the advancement of biomarker-driven precision dosing.Clinical and translational science · 2021Article
- Characteristics, Symptom Severity, and Experiences of Patients Reporting Chronic Kidney Disease in the PatientsLikeMe Online Health Community: Retrospective and Qualitative Study.Journal of medical Internet research · 2020Article
- Research data management in health and biomedical citizen science: practices and prospects.JAMIA open · 2020Article
- Characteristics and Symptom Severity of Patients Reporting Systemic Lupus Erythematosus in the PatientsLikeMe Online Health Community: A Retrospective Observational Study.Rheumatology and therapy · 2020Article
- Dealing with internet-based information obtained by families of critically ill patients.Intensive care medicine · 2019Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundLaunched in 2006 for patients with amyotrophic lateral sclerosis, PatientsLikeMe is an online community offering patient-reported outcomes, symptom tracking, and social features. Every member of the site can see all the data reported by every other member, view aggregated reports, identify "patients like them," and learn about treatment options in order to live better with their condition. In previous studies, members reported benefits such as improved condition knowledge, increased medication adherence, and better management of side effects. However, the site evolved in 2011 from condition-specific "vertical" communities consisting only of people with the same disease to a "generalized platform," in which every patient could connect with every other patient regardless of condition and with generic, rather than condition-specific, data tools. Some, but not all, communities received further custom tracking tools.
objectiveWe aimed to understand (1) whether members of PatientsLikeMe using the generalized platform still reported similar benefits and (2) assess factors associated with benefits, such as community customization, site use, and patient activation.
methodsA cross-sectional retrospective custom survey was fielded to 377,625 members between 2016 and 2017 including the Patient Activation Measure (PAM). A benefit index was developed for comparability across conditions.
resultsThe invitation was viewed by 26,048 members of whom 11,915 did not respond, 5091 opted out, 1591 provided partial data, and 17 were screened out. Complete responses were received from 7434 participants. Users perceived greatest benefit in understanding how their condition may affect them (4530/6770, 66.91% participants, excluding "does not apply" answers), understanding what might help them live better with their condition (4247/6750, 62.92%), which treatments were available (4143/6898, 60.06%), understanding treatment side effects (4182/6902, 60.59%), and important factors in making treatment decisions (3919/6813, 57.52%). The benefit index was 29% higher for the "most activated" patients (PAM level 4 vs PAM level 1; relative risk [RR]=1.29, P<.001), 21% higher for conditions with some community customization versus none (RR=1.21, P<.001), and 11% higher in those using the site most often versus least (RR=1.11, P<.001).
conclusionsMembers of the generalized platform reported a range of benefits related to improved knowledge and understanding of their condition and treatment management. Condition-specific customization may improve their experience still further. Future studies will explore longitudinal changes to patient activation.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.