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Exploring Communication Ability in Individuals With Angelman Syndrome: Findings From Qualitative Interviews With Caregivers.
Zigler, Christina K; Lucas, Nicole; McFatrich, Molly; Gordon, Kelly L; Jones, Harrison N; Berent, Allyson; Panagoulias, Jennifer; Evans, Paula; Reeve, Bryce B.
Afiliación
  • Zigler CK; Christina K. Zigler, Nicole Lucas, and Molly McFatrich, Duke University School of Medicine.
  • Lucas N; Christina K. Zigler, Nicole Lucas, and Molly McFatrich, Duke University School of Medicine.
  • McFatrich M; Christina K. Zigler, Nicole Lucas, and Molly McFatrich, Duke University School of Medicine.
  • Gordon KL; Kelly L. Gordon, Duke Health.
  • Jones HN; Harrison N. Jones, Duke University School of Medicine.
  • Berent A; Allyson Berent, Jennifer Panagoulias, and Paula Evans, The Foundation for Angelman Syndrome Therapceutis (FAST).
  • Panagoulias J; Allyson Berent, Jennifer Panagoulias, and Paula Evans, The Foundation for Angelman Syndrome Therapceutis (FAST).
  • Evans P; Allyson Berent, Jennifer Panagoulias, and Paula Evans, The Foundation for Angelman Syndrome Therapceutis (FAST).
  • Reeve BB; Bryce B. Reeve, Duke University School of Medicine.
Am J Intellect Dev Disabil ; 128(3): 185-203, 2023 05 01.
Article en En | MEDLINE | ID: mdl-37104863
ABSTRACT
Communication deficits have a substantial impact on quality of life for individuals with Angelman syndrome (AS) and their families, but limited qualitative work exists to support the necessary content of measures aiming to assess communication for these individuals. Following best practices for concept elicitation studies, we conducted individual qualitative interviews with caregivers and clinicians to elicit meaningful aspects of communication for individuals with AS. Caregivers were able to discuss their child's specific communication behaviors within a large number of expressive, receptive, and pragmatic functions via numerous symbolic and non-symbolic modalities. These results aligned well with published literature on communication in AS and will be used to inform the design of a novel caregiver-reported measure. Future studies on communication in individuals with AS should focus on gathering quantitative data from large samples of diverse caregivers, which would allow for estimations of the frequency of specific behaviors across the population.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cuidadores / Síndrome de Angelman Tipo de estudio: Diagnostic_studies / Guideline / Qualitative_research Aspecto: Patient_preference Límite: Child / Humans Idioma: En Revista: Am J Intellect Dev Disabil Asunto de la revista: TRANSTORNOS MENTAIS Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cuidadores / Síndrome de Angelman Tipo de estudio: Diagnostic_studies / Guideline / Qualitative_research Aspecto: Patient_preference Límite: Child / Humans Idioma: En Revista: Am J Intellect Dev Disabil Asunto de la revista: TRANSTORNOS MENTAIS Año: 2023 Tipo del documento: Article