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1.
J Appl Res Intellect Disabil ; 37(5): e13282, 2024 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-39074852

RESUMEN

BACKGROUND: The aim of this feasibility study was to adapt and model a behavioural intervention for anxiety with autistic adults with moderate to severe intellectual disabilities. METHOD: Twenty-eight autistic adults with moderate or severe intellectual disabilities, 37 carers, and 40 therapists took part in this single-group non-randomised feasibility study designed to test intervention feasibility and acceptability, outcome measures, and research processes. RESULTS: The intervention was judged as feasible and acceptable by autistic adults with intellectual disabilities, carers, and therapists. Minor intervention revisions were suggested. Carers completed 100% of outcome measures and the missing data rate was low. Complying with legislation governing the inclusion of participants who lack capacity to decide whether they wanted to take part in this study led to an average 5-week enrolment delay. CONCLUSION: The intervention and associated study processes were judged to be feasible and acceptable and should now be tested within a larger randomised trial.


Asunto(s)
Trastorno Autístico , Terapia Conductista , Estudios de Factibilidad , Discapacidad Intelectual , Humanos , Discapacidad Intelectual/terapia , Adulto , Masculino , Femenino , Trastorno Autístico/terapia , Terapia Conductista/métodos , Adulto Joven , Persona de Mediana Edad , Ansiedad/terapia , Trastorno del Espectro Autista/terapia
2.
J Autism Dev Disord ; 45(5): 1238-53, 2015 May.
Artículo en Inglés | MEDLINE | ID: mdl-25491025

RESUMEN

Syndrome specific repetitive behavior profiles have been described previously. A detailed profile is absent for Rubinstein-Taybi syndrome (RTS). The Repetitive Behaviour Questionnaire and Social Communication Questionnaire were completed for children and adults with RTS (N = 87), Fragile-X (N = 196) and Down (N = 132) syndromes, and individuals reaching cut-off for autism spectrum disorder (N = 228). Total and matched group analyses were conducted. A phenotypic profile of repetitive behavior was found in RTS. The majority of behaviors in RTS were not associated with social-communication deficits or degree of disability. Repetitive behavior should be studied at a fine-grained level. A dissociation of the triad of impairments might be evident in RTS.


Asunto(s)
Trastornos Generalizados del Desarrollo Infantil/diagnóstico , Conducta Compulsiva/diagnóstico , Síndrome de Down/diagnóstico , Síndrome del Cromosoma X Frágil/diagnóstico , Síndrome de Rubinstein-Taybi/diagnóstico , Adolescente , Adulto , Niño , Trastornos Generalizados del Desarrollo Infantil/complicaciones , Preescolar , Trastornos de la Comunicación/complicaciones , Trastornos de la Comunicación/diagnóstico , Conducta Compulsiva/complicaciones , Estudios Transversales , Síndrome de Down/complicaciones , Femenino , Síndrome del Cromosoma X Frágil/complicaciones , Humanos , Masculino , Persona de Mediana Edad , Síndrome de Rubinstein-Taybi/complicaciones , Evaluación de Síntomas , Adulto Joven
3.
J Autism Dev Disord ; 41(8): 1019-32, 2011 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-21080217

RESUMEN

We investigated autism spectrum disorder (ASD) symptomatology, hyperactivity and affect in seven genetic syndromes; Angelman (AS; n = 104), Cri du Chat (CdCS; 58), Cornelia de Lange (CdLS; 101), Fragile X (FXS; 191), Prader-Willi (PWS; 189), Smith-Magenis (SMS; 42) and Lowe (LS; 56) syndromes (age range 4-51). ASD symptomatology was heightened in CdLS and FXS. High levels of impulsivity were seen in SMS, AS, CdCS, FXS and adults with CdLS. Negative affect was prominent in adults with CdLS, while positive affect was prominent in adults with AS and FXS. Heightened levels of overactivity and impulsivity were identified in FXS, AS and SMS while low levels were identified in PWS. These findings confirm and extend previously reported behavioral phenotypes.


Asunto(s)
Afecto , Trastornos Generalizados del Desarrollo Infantil/complicaciones , Trastornos de los Cromosomas/complicaciones , Hipercinesia/complicaciones , Adolescente , Adulto , Niño , Trastornos Generalizados del Desarrollo Infantil/genética , Trastornos Generalizados del Desarrollo Infantil/psicología , Preescolar , Trastornos de los Cromosomas/genética , Trastornos de los Cromosomas/psicología , Femenino , Humanos , Hipercinesia/genética , Hipercinesia/psicología , Masculino , Persona de Mediana Edad , Fenotipo
4.
J Autism Dev Disord ; 39(4): 572-88, 2009 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19037716

RESUMEN

We investigated the prevalence and phenomenology of repetitive behavior in genetic syndromes to detail profiles of behavior. The Repetitive Behaviour Questionnaire (RBQ) provides fine-grained identification of repetitive behaviors. The RBQ was employed to examine repetitive behavior in Angelman (N = 104), Cornelia de Lange (N = 101), Cri-du-Chat (N = 58), Fragile X (N = 191), Prader-Willi (N = 189), Lowe (N = 56) and Smith-Magenis (N = 42) syndromes and individuals with intellectual disability of heterogeneous aetiology (N = 56). Repetitive behavior was variable across syndromes. Fragile X syndrome scored highly on all subscales. Angelman syndrome demonstrated a significantly lowered probability for most behaviors. Prader-Willi, Cri-du-Chat and Smith-Magenis syndrome evidenced unique profiles of repetitive behavior. There is extreme heterogeneity of repetitive behavior across genetic syndromes, highlighting syndrome specific profiles.


Asunto(s)
Discapacidad Intelectual/epidemiología , Discapacidad Intelectual/psicología , Conducta Estereotipada , Adolescente , Adulto , Síndrome de Angelman/epidemiología , Síndrome de Angelman/psicología , Niño , Preescolar , Síndrome del Maullido del Gato/epidemiología , Síndrome del Maullido del Gato/psicología , Síndrome de Cornelia de Lange/epidemiología , Síndrome de Cornelia de Lange/psicología , Femenino , Síndrome del Cromosoma X Frágil/epidemiología , Síndrome del Cromosoma X Frágil/psicología , Humanos , Discapacidad Intelectual/genética , Londres , Masculino , Persona de Mediana Edad , Fenotipo , Síndrome de Prader-Willi/epidemiología , Síndrome de Prader-Willi/psicología , Prevalencia , Encuestas y Cuestionarios , Síndrome , Adulto Joven
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