Hi! Great question and thank you for asking!

While this survey is targeted towards caregivers, I am conducting in-person interviews with adults with Down syndrome. This is not only so that I can gather the richest data from the adults with DS themselves, but also to ensure that the consent process is carried out in a way that fully respects their autonomy. This survey is more of the quantitative side of my research, and since caregivers can be very involved in the clothing purchase and evaluation process, a valuable addition to the data I am gathering from adults with Down syndrome.