Lyme-COS aims to find out what outcomes of treatment for Lyme borreliosos (Lyme disease) are most important to health professionals, researchers and people who have or have had Lyme disease.
An outcome is something that we measure in research studies to find out if a treatment is working or not. The outcomes measured should be important to health professionals, researchers and patients. You can find out more about outcomes and core outcome sets in the short video below.
If you are a health professional or researcher working in the field of Lyme borreliosis or you are a patient who has had or has Lyme borreliosis (Lyme disease) then you can have your say on important outcomes by taking part in the Lyme-COS study. Taking part will involve completing two short online surveys.
Taking part will involve completing two short online surveys that will be available later in the year.
To get more information and an invitation to take part in the surveys when the study opens please register your name and contact email address. We will only contact you with information about the Lyme-COS study and there is no obligation to take part.
This study is funded by Lyme Disease Action and is coordinated and led by the University of Liverpool and the COMET Initiative together with an International steering committee of health professionals and patients.