Get involved
We are looking for participants for the Converge study and would love to hear from you if you or your family are eligible.
Who can take part?
Young people aged between 10-25 years who have been diagnosed with a 22q11.2 deletion, 16p11.2 duplication, or 1q21.1 deletion are invited to participate.
Where possible, we would invite siblings between the ages of 10-25 years to also take part, so that we can explore how having a CNV may contribute to any changes in brain structure and function.
How to take part
If you're interested in participating, email Converge, and we will respond as soon as possible.
What does the study involve?
Taking part will involve travelling to Cardiff. We are happy to work flexibly around time schedules that best suit your family. All travel, hotel, and expenses for your visit will be covered.
We will use both magnetic resonance imaging (MRI) and magnetoencephalography (MEG) brain scans as part of the study. These scans are completely non-invasive and do not involve any injections.
In addition, we would like to do some computer games and activities with your child to learn more about their coordination and movement. Your child will also be asked some questions about their mood, feelings, behaviours, and experiences at school.
And, if possible, we would also like to collect a small blood or saliva sample from you and your children.
Reimbursement
Any travel costs and any costs for accommodation incurred as part of the study will be reimbursed. Your family will receive a £30 shopping voucher as a thank you for taking part. Participating children will also receive a small gift to show our appreciation for their contribution.
You will also receive a personal summary report of your child’s strengths and difficulties. You may find this report a useful summary if your child has assessments for services, school, or specialist treatments.
Finally, joining Converge gives you a chance to help learn more about children living with rare genetic conditions. Your contribution will help other families to gain better information about their child’s development and behaviour.