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Scaling PatientsLikeMe via a 'Generalized Platform' for Members with Chronic Illness: Web-Based Survey Study of Benefits Arising
- Source :
- Journal of Medical Internet Research
- Publication Year :
- 2018
- Publisher :
- JMIR Publications, 2018.
-
Abstract
- Background: Launched 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. Objective: We 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. Methods: A 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. Results: The 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
- Subjects :
- online support group
Male
medicine.medical_specialty
020205 medical informatics
Cross-sectional study
self-help devices
Health Informatics
02 engineering and technology
Disease
03 medical and health sciences
Social support
0302 clinical medicine
personal health records
Surveys and Questionnaires
Health care
0202 electrical engineering, electronic engineering, information engineering
Medicine
Humans
personal monitoring
personal tracking
Patient participation
Retrospective Studies
Patient Activation Measure
Original Paper
Internet
business.industry
Amyotrophic Lateral Sclerosis
Social Support
Retrospective cohort study
online health community
Middle Aged
Online community
health care
Cross-Sectional Studies
Family medicine
technology
Chronic Disease
Female
Patient Participation
business
030217 neurology & neurosurgery
Subjects
Details
- Language :
- English
- ISSN :
- 14388871 and 14394456
- Volume :
- 20
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Journal of Medical Internet Research
- Accession number :
- edsair.doi.dedup.....2ce13999881d16603f70f1d04b2e3ae4