FAQs

What is the Genetic Links to Anxiety and Depression (GLAD) Study?
How do I sign up to the GLAD Study?
How do genetics and the environment influence the development of anxiety and depression?
What is a control participant?
Why is the GLAD Study recruiting a control group?
Can I still take part if I haven’t received a diagnosis or treatment?
Should I still send back my saliva sample if I am feeling unwell?
What should I do if I feel distressed?
I have signed up and completed all 4 steps in GLAD. Is there anything more I can do to contribute?
How will you use the survey, biological and genetic information data I give you?
What research has been published using data from the GLAD Study?
What is GLAD doing to strive for equality, diversity, and inclusion?
What is the NIHR BioResource?
How is the information I give you kept confidential?
Will commercial companies be accessing my data?
Why do you need access to my medical records?
How will you access my medical records?
What sections of my medical records will you access?
What will you do with my medical records?
What other studies might I be invited to take part in?