Quality of life outcomes and predictors for youth with intellectual disability and rare diseases

The concept of quality of Life (QoL) has become particularly relevant in the field of intelectual disability (ID). However, the existing scientific literature on QoL of people with ID and rare diseases (RDs) is very limited. Therefore, this study aimed to analyze individual QoL of children and youth...

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Detalles Bibliográficos
Autores: Morán Suárez, María Lucía|||0000-0001-5650-6711, Monsalve González, Asunción, Fontanil, Yolanda, Bacherini, Alice, Balboni, Giulia, Gómez Sánchez, Laura Elisabet
Tipo de recurso: artículo
Fecha de publicación:2025
País:España
Institución:Universidad de Cantabria (UC)
Repositorio:UCrea Repositorio Abierto de la Universidad de Cantabria
Idioma:inglés
OAI Identifier:oai:repositorio.unican.es:10902/39665
Acceso en línea:https://hdl.handle.net/10902/39665
Access Level:acceso abierto
Palabra clave:Intellectual developmental disorder
Fragile X syndrome
West syndrome
Children Adolescents
Young adults
Descripción
Sumario:The concept of quality of Life (QoL) has become particularly relevant in the field of intelectual disability (ID). However, the existing scientific literature on QoL of people with ID and rare diseases (RDs) is very limited. Therefore, this study aimed to analyze individual QoL of children and youth with RDs and to evaluate the impact of personal and contextual factors on their QoL. The sample was composed of 114 Spanish participants with ID and RDs, aged between 4 and 21 years. The KidsLife Scale was applied. This instrument includes 96 items, third-person ormulated, organized across eight QOL domains: physical wellbeing, material wellbeing, emotional wellbeing, interpersonal relationships, social inclusion, rights and personal development. Descriptive statistics were calculated and correlation coefficients and multiple linear regression were computed. The most elevated scores were achieved in physical well-being and material wellbeing, whereas the lowest scores were shown in social inclusion and self-determination domains. Sex, level of support needs, percentage of disability and size of the organization were predictive factors of QoL scores. These outcomes shed light into priority areas and predictors that should be considered in the development of individualized supports, organizational approaches and policy initiatives intended to promote the QoL of children and youth with RDs and ID.