ArticleResearch involvement and engagement2016
Patients' motivations and interest in research: characteristics of volunteers for patient-led projects on PatientsLikeMe.
Article in Research involvement and engagement, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
20 citing papers in PubMed.
- Building a diverse national research advisory board.Journal of clinical and translational science · 2025Article
- Willingness of population health survey participants to provide personal health information and biological samples.BMC public health · 2024Article
- Understanding the Patient Perspective When Designing Future Rehabilitation Interventions after Hip or Knee Replacement Surgery-A Patient and Public Involvement Exercise.Medicina (Kaunas, Lithuania) · 2023Article
- Commitments for Ethically Responsible Sourcing, Use, and Reuse of Patient Data in the Digital Age: Cocreation Process.Journal of medical Internet research · 2023Article
- So You Want to Build Your Disease's First Online Patient Registry: An Educational Guide for Patient Organizations Based on US and European Experience.The patient · 2023Article
- Developing a research community within an online healthcare feedback platform.Health expectations : an international journal of public participation in health care and health policy · 2023Article
- Motivators and barriers towards clinical research participation: A population-based survey from an Arab MENA country.PloS one · 2022Article
- Audience of Academic Otolaryngology on Twitter: Cross-sectional Study.JMIR medical education · 2021Article
- What motivates informal carers to be actively involved in research, and what obstacles to involvement do they perceive?Research involvement and engagement · 2021Article
- A feasibility evaluation of Discovery Group: determining the acceptability and potential outcomes of a patient-led research group in a secure mental health inpatient setting.Research involvement and engagement · 2021Article
- The CORBEL matrix on informed consent in clinical studies: a multidisciplinary approach of Research Infrastructures Building Enduring Life-science Services.BMC medical ethics · 2021Review
- A Qualitative Analysis of Motivators to Participation in Suicide-Focused Research from a Community-Based Australian Sample.International journal of environmental research and public health · 2021Article
- Patients and Partners in Research: Patient and Caregiver Perceptions of Research Engagement and the Role of Their Psychosocial States in Participation.Journal of patient experience · 2021Article
- Patient Satisfaction in Emergency General Surgery: A Prospective Cross-Sectional Study.World journal of surgery · 2020Article
- Article
- Evaluation of a project to engage patients in the development of a patient-reported measure for HIV care (the I-Score Study).Health expectations : an international journal of public participation in health care and health policy · 2019Article
- Sharing individual participant data from clinical studies: a cross-sectional online survey among Italian patient and citizen groups.BMJ open · 2019Article
- How Returning Aggregate Research Results Impacts Interest in Research Engagement and Planned Actions Relevant to Health Care Decision Making: Cohort Study.Journal of medical Internet research · 2018Article
- Article
- Recruiting patients as partners in health research: a qualitative descriptive study.Research involvement and engagement · 2017Article
Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
plain english summaryPLM is an online platform that provides tools for individuals to track their health and connect with other patients and while PLM has invited patients to participate in various research projects throughout the years, an examination into what motivates patients to
backgroundHistorically, throughout the clinical and medical research arenas, patients have been perceived as passive "subjects" rather than as individuals who may have thoughts regarding research development, research plans, implementation of research studies, and data analysis. However, it is becoming more clear that patients increasingly want to have a more active role in clinical research studies and in the management of their own medical conditions as evidenced by a "no decision about us without us" stance, meaning patients want to make informed decisions about their health while working alongside their healthcare professionals. The central aim of this research study was to determine patients' motivations for being involved in research design and understand their perceptions of current research practices.
methodsTwo independent qualitative studies were conducted. In Study 1, we analyzed applications submitted by self-identified patients from within the PatientsLikeMe (PLM) community, for acceptance onto our advisory panel. The advisory panel was tasked with developing a best practice guide for how to involve patients in research. During the qualitative analysis, we identified major reasons for and topics of interest associated with PLM members' motivation to apply to the advisory panel. In Study 2, we analyzed applications from PLM community members and from patients outside the PLM community for a patient-led patient-reported-outcome (PRO) development project. Similar to Study 1, we identified themes associated with patients' motivations to participate in developing a new PRO.
resultsPLM members are interested in being involved in medical research for various reasons, including facilitating provider-patient communication, improving comprehension of medical information, understanding their disease, and bringing a more individualized approach to health care in general.
conclusionChallenges in the process of appropriate involvement of patients in research are discussed. In both studies, the applicants shared their interests in being involved in research. However, in Study 2, many of the patients shared ideas that were not appropriate for the development of a PRO, which indicated limitations in how the invitation and application explained the project to patients. Future studies should contribute to determining the most appropriate method for involving patients in various settings.
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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.