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Even less attention has been given to pediatric populations. To understand patients\u2019 views about identity changes due to DBS in obsessive-compulsive disorder (OCD), the authors conducted and analyzed semistructured interviews with adolescent patients with OCD and their parents\/caregivers. Patients were asked about projected impacts to PIA generally due to DBS. All patient respondents and half of caregivers reported that DBS would impact patient self-identity in significant ways. For example, many patients expressed how DBS could positively impact identity by allowing them to explore their identities free from OCD. Others voiced concerns that DBS-related resolution of OCD might negatively impact patient agency and authenticity. Half of patients expressed that DBS may positively facilitate social access through relieving symptoms, while half indicated that DBS could increase social stigma. These views give insights into how to approach decision-making and informed consent if DBS for OCD becomes available for adolescents. They also offer insights into adolescent experiences of disability identity and \u201cnormalcy\u201d in the context of OCD.<\/jats:p>","DOI":"10.1017\/s0963180124000203","type":"journal-article","created":{"date-parts":[[2024,4,11]],"date-time":"2024-04-11T08:43:05Z","timestamp":1712824985000},"page":"507-520","source":"Crossref","is-referenced-by-count":3,"title":["Adolescent OCD Patient and Caregiver Perspectives on Identity, Authenticity, and Normalcy in Potential Deep Brain Stimulation Treatment"],"prefix":"10.1017","volume":"33","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2787-3798","authenticated-orcid":false,"given":"Jared 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