About 50% of children and adolescents with intellectual disability have a mental disorder or serious behavior problems;this is three times as high as is found in typically developing youth. This "dual diagnosis" (intellectual disability and mental disorder) puts them at much heightened risk for a host of unfavorable long- term life outcomes. Too, these youth present major coping and health challenges to their families and also economic challenges to the service delivery system. While there are certainly some syndrome-related contributions to dual diagnosis, most children with mild or borderline intellectual disability do not have identified genetic syndromes. There have been dramatic advances in developmental psychopathology in addressing the basic questions of continuity of mental disorder across childhood, and the mechanisms by which risk and protective factors have an influence. Unfortunately, youth with intellectual disability are routinely excluded from most studies, so there has been little advance in our understanding of prevention of dual diagnosis. This is a proposal to continue the Collaborative Family Study, a unique longitudinal prospective study that focuses on the development of psychopathology and social competence in youth with intellectual disability;there is also a contrasting group of typically developing youth. The primary aim is to determine the emergence and continuity of psychopathology from early childhood through adolescence, and to understand the dynamic influences of early and ongoing family processes, as well as school experiences, on regulatory capacities and outcomes for children with and without intellectual disability. The CFS has assessed 190 children and their families annually from child age 3 to 9 years, obtaining in- depth child developmental assessments, naturalistic and structured observations of parent-child interactions and children's emotional and behavioral regulation, comprehensive reports of parent and child functioning, and assessments from the children's schools. Findings to date indicate that early family processes do relate to the child's self-regulatory abilities and child subsequent challenging behaviors, which, in turn, increase stress and impair mental and physical health in the child's family. We propose continuing the CFS through early adolescence (ages 12 13, 15), when risk for many mental disorders increases. We will recruit an additional sample (n=90) that will be at least 60% Hispanic, and study the relationships between family processes and youths'psychopathology and social competence within two prominent cultural groups (Hispanics and non- Hispanic Whites). This study has direct public health relevance, given the enormity of the problem of mental disorder in intellectual disability. Findings about the course and causes of psychopathology in these youth could inform prevention and early intervention programs, as well as parent education programs through adolescence, school curricula, and therapeutic programs for the youth themselves.
Children with intellectual disability (mental retardation) are about three times as likely to have mental disorders or serious behavior problems as are typically developing children, but little is known about causes. This prospective longitudinal study, from child age 3 to 15 years, is assessing child, family, school, and cultural influences on the development of psychopathology and social competence in children and adolescents with intellectual disability and a typically developing comparison group. It has direct public health relevance, as findings about the course and causes of psychopathology in these youth could inform the content of prevention and early intervention programs, as well as parent education programs, school curricula, and therapeutic programs for the youth themselves.
|Green, Shulamite A; Berkovits, Lauren D; Baker, Bruce L (2015) Symptoms and development of anxiety in children with or without intellectual disability. J Clin Child Adolesc Psychol 44:137-44|
|Zeedyk, S M; Rodriguez, G; Tipton, L A et al. (2014) Bullying of youth with autism spectrum disorder, intellectual disability, or typical development: Victim and parent perspectives. Res Autism Spectr Disord 8:1173-1183|
|Ciciolla, Lucia; Gerstein, Emily D; Crnic, Keith A (2014) Reciprocity among maternal distress, child behavior, and parenting: transactional processes and early childhood risk. J Clin Child Adolesc Psychol 43:751-64|
|Fenning, Rachel M; Baker, Jason K; Baker, Bruce L et al. (2014) Parent-child interaction over time in families of young children with borderline intellectual functioning. J Fam Psychol 28:326-35|
|Eisenhower, Abbey; Blacher, Jan; Baker, Bruce L (2013) Mothers' perceived physical health during early and middle childhood: relations with child developmental delay and behavior problems. Res Dev Disabil 34:1059-68|
|Ciciolla, Lucia; Crnic, Keith A; West, Stephen G (2013) Determinants of Change in Maternal Sensitivity: Contributions of Context, Temperament, and Developmental Risk. Parent Sci Pract 13:178-195|
|Neece, Cameron L; Baker, Bruce L; Lee, Steve S (2013) ADHD among adolescents with intellectual disabilities: pre-pathway influences. Res Dev Disabil 34:2268-79|
|Blacher, Jan; Baker, Bruce L; Kaladjian, Araksia (2013) Syndrome specificity and mother-child interactions: examining positive and negative parenting across contexts and time. J Autism Dev Disord 43:761-74|
|Stevenson, Matthew M; Crnic, Keith A (2013) Activative Fathering Predicts Later Children's Behaviour Dysregulation and Sociability. Early Child Dev Care 183:774-790|
|Begum, Gazi; Blacher, Jan (2011) The siblings relationship of adolescents with and without intellectual disabilities. Res Dev Disabil 32:1580-8|
Showing the most recent 10 out of 29 publications