Patient experience research is any research activity that seeks to understand the experiences, attitudes and opinions of patients as it relates to their health and interactions with the healthcare system.
Patient experience research is considered “non-interventional”: meaning that no treatment is given and no medical tests are administered. Researchers simply want to hear from patients and caregivers about their true lived experiences and understand their needs.
Our mission is to elevate the patient voice to key decision-makers in the healthcare industry. That’s why we created this community.
By joining the Research Opportunities community, you can join us in our mission. We will use this community to connect to patients and provide you with opportunities to participate in patient experience research through various individual or group discussions, polls, and surveys.
Written by
AnnaHU
HealthUnlocked
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I am happy for the research and happy to share my lived experience and needs and interactions with healthcare system if it goes towards improving and elevating the patient voice as much needed for a better healthcare system for both patient and medics
since being diagnosed with PMR in Aug 2020 I have felt that this condition is the poor relation of other autoimmune conditions & any research will be of benefit to others like me who had never heard of the condition before. Thanks
I am interested in participating in patient research if it can help in any way to minimise the Restless Leg experience suffered by so many of us on this forum.
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