The national council for osteopathic research with many motivated osteopaths has been collecting data from osteopathic patients over the last 6 years. We have been asking patients about themselves, their consultations and care, what happens to their symptoms and health, what they experience and whether they are satisfied. We now have a substantial database and during this webinar we will summarise this information and show how you too can collect data and learn more about your patients. By the end of this webinar you will be familiar with the concept of patient-reported outcomes and how they can be useful for practice.
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