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Showing 1 to 15 of 73 results Save | Export
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Hirvonen, M.; Ojala, R.; Korhonen, P.; Haataja, P.; Eriksson, K.; Rantanen, K.; Gissler, M.; Luukkaala, T.; Tammela, O. – Journal of Intellectual Disability Research, 2017
Background: Prematurity has been shown to be associated with an increased risk of intellectual disability (ID). Method: The aim was to establish whether the prevalence of ID, defined as significant limitations in both intellectual (intelligence quotient below 70) and adaptive functioning among moderately preterm (MP; 32[superscript + 0]-33…
Descriptors: Intellectual Disability, Young Children, Premature Infants, Incidence
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Boström, P.; Åsberg Johnels, J.; Broberg, M. – Journal of Intellectual Disability Research, 2018
Background: The Wellbeing in Special Education Questionnaire was developed to assess subjective wellbeing in young persons with intellectual and developmental disabilities (ID/DD) as this perspective is rarely included in research. The present study explored how ID/DD and gender are related to self-reported wellbeing among adolescents. Method:…
Descriptors: Well Being, Gender Differences, Intellectual Disability, Peer Relationship
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Shimoyama, M.; Iwasa, K.; Sonoyama, S. – Journal of Intellectual Disability Research, 2018
Background: People with intellectual disabilities are more likely than people in the general population to experience life events associated with an increased risk of mental health problems. However, there has been little research in Japan on the prevalence of mental health problems in adults with intellectual disability (ID) or on associated…
Descriptors: Intellectual Disability, Mental Disorders, At Risk Persons, Foreign Countries
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Raspa, M.; Fitzgerald, T.; Furberg, R. D.; Wylie, A.; Moultrie, R.; DeRamus, M.; Wheeler, A. C.; McCormack, L. – Journal of Intellectual Disability Research, 2018
Background: Little is known about how individuals with fragile X syndrome (FXS) and their families use technology in daily life and what skills individuals with FXS can perform when using mobile technologies. Methods: Using a mixed-methods design, including an online survey of parents (n = 198) and a skills assessment of individuals with FXS (n =…
Descriptors: Telecommunications, Handheld Devices, Intellectual Disability, Parent Attitudes
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Jahoda, A.; Pownall, J. – Journal of Intellectual Disability Research, 2014
Background: Sexual development plays a vital part in young people's emotional adjustment. Method: This study compared the sexual understanding of 30 adolescents with mild intellectual disabilities (ID) and 30 non-disabled adolescents, along with their reports of where they obtained sexual information, and the nature of their social networks…
Descriptors: Sexuality, Adolescents, Mild Mental Retardation, Knowledge Level
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Mileviciute, I.; Hartley, S. L. – Journal of Intellectual Disability Research, 2015
Background: Virtually nothing is known about potential differences in the types of depression symptoms reported by adults with mild intellectual disability (ID) on self-reported questionnaires as compared with the types of symptoms reported by caregivers on informant questionnaires. Moreover, little is known about how the presentation of…
Descriptors: Symptoms (Individual Disorders), Depression (Psychology), Adults, Mild Mental Retardation
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Kiani, R.; Tyrer, F.; Jesu, A.; Bhaumik, S.; Gangavati, S.; Walker, G.; Kazmi, S.; Barrett, M. – Journal of Intellectual Disability Research, 2014
Background: People with intellectual disability (ID) and epilepsy are more likely to die prematurely than the general population. A significant number of deaths in people with epilepsy may be potentially preventable through better seizure control, regular monitoring and raising awareness among patients and carers. The aim of this project was to…
Descriptors: Death, Seizures, Epilepsy, Mental Retardation
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Shashi, V.; Harrell, W.; Eack, S.; Sanders, C.; McConkie-Rosell, A.; Keshavan, M. S.; Bonner, M. J.; Schoch, K.; Hooper, S. R. – Journal of Intellectual Disability Research, 2015
Background: Children with chromosome 22q11.2 deletion syndrome (22q11DS) often have deficits in social cognition and social skills that contribute to poor adaptive functioning. These deficits may be of relevance to the later occurrence of serious psychiatric illnesses such as schizophrenia. Yet, there are no evidence-based interventions to improve…
Descriptors: Social Cognition, Feasibility Studies, Intervention, Interpersonal Competence
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Lindsay, W.; Steptoe, L.; Haut, F. – Journal of Intellectual Disability Research, 2012
Background: Some studies have found higher rates of childhood sexual abuse in sex offenders while others have failed to find such relationships. Method: This study reviews the sexual and physical abuse histories of 156 male sex offenders with intellectual disability (ID), 126 non-sexual male offenders with ID and 27 female offenders with ID.…
Descriptors: Child Abuse, Criminals, Gender Differences, Sexual Abuse
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Memisevic, H.; Sinanovic, O. – Journal of Intellectual Disability Research, 2014
Background: Executive function is very important in the children's overall development. The goal of this study was to assess the executive function in children with intellectual disability (ID) through the use of the Behavior Rating Inventory of Executive Function (BRIEF) teacher version. An additional goal was to examine the differences in…
Descriptors: Mental Retardation, Etiology, Executive Function, Gender Differences
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Pozo, P.; Sarriá, E.; Brioso, A. – Journal of Intellectual Disability Research, 2014
Background: This study examined family quality of life (FQOL) and psychological well-being from a multidimensional perspective. The proposed model was based on the double ABCX model, with severity of the disorder, behaviour problems, social support, sense of coherence (SOC) and coping strategies as components. Method: One hundred and eighteen…
Descriptors: Autism, Pervasive Developmental Disorders, Quality of Life, Family Life
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Reilly, C.; Senior, J.; Murtagh, L. – Journal of Intellectual Disability Research, 2015
Background: A number of neurogenetic syndromes have a high association with special educational needs including fragile X syndrome (FXS), Prader-Willi syndrome (PWS), Williams syndrome (WS) and Velo-Cardio-Facial syndrome (VCFS). There is a paucity of research on educational provision for children affected by these syndromes. Method: Parents…
Descriptors: Neurological Impairments, Genetic Disorders, Special Education, Student Needs
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Mercier, C.; Picard, S. – Journal of Intellectual Disability Research, 2011
Background: The association between poverty and intellectual disability (ID) has been well documented. However, little is known about persons with ID who face circumstances of extreme poverty, such as homelessness. This paper describes the situation of persons with ID who were or are homeless in Montreal and are currently receiving services from a…
Descriptors: Homeless People, Mental Retardation, Poverty, Gender Differences
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Klusek, J.; Martin, G. E.; Losh, M. – Journal of Intellectual Disability Research, 2014
Background: Prior research suggests that 60-74% of males and 16-45% of females with fragile X syndrome (FXS) meet criteria for autism spectrum disorder (ASD) in research settings. However, relatively little is known about the rates of clinical diagnoses in FXS and whether such diagnoses are consistent with those performed in a research setting…
Descriptors: Genetic Disorders, Pervasive Developmental Disorders, Autism, Clinical Diagnosis
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Giltaij, H. P.; Sterkenburg, P. S.; Schuengel, C. – Journal of Intellectual Disability Research, 2015
Background: Children with intellectual disability (ID) are at risk for maladaptive development of social relatedness. Controversy exists whether Pervasive Developmental Disorder (PDD) takes precedence over disordered attachment for describing maladaptive social behaviour. The aim of this study was to assess the prevalence of disordered attachment…
Descriptors: At Risk Persons, Children, Interpersonal Competence, Pervasive Developmental Disorders
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