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      Parental Burden and its Correlates in Families of Children with Autism Spectrum Disorder: A Multicentre Study with Two Comparison Groups

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          Abstract

          Background:

          The effects of having a child with Autism Spectrum Disorder (ASD) on parents are multifaceted and pervasive. While ample evidence has been provided that these families are under severe stress, there are still several knowledge gaps and unresolved questions.

          Objective:

          This study aimed at quantifying the subjective and objective burden of ASD in mothers and fathers, and at improving the understanding of the interplay between parental burden, child’s characteristics, and parents’ coping resources and strategies.

          Methods:

          The parents of 359 children/adolescents with ASD were compared to parents of age-matched patients with Down syndrome (N=145) and Type 1 diabetes mellitus (N=155). Child’s clinical characteristics and parents’ caregiving burden, psychological distress, coping resources and strategies were assessed.

          Results:

          The parents of children with ASD reported higher objective and subjective burden, more frequent psychological distress, lower social support. Mothers reported greater subjective burden than fathers. Structural equation modeling showed that the most consistent positive and negative predictors of objective and subjective burden were ASD symptom severity and social support, respectively. Other positive predictors were engagement, distraction and disengagement coping, intellectual disability, and adaptive functioning. Other negative predictors were spiritual wellbeing and hardiness. Some effects were indirect through social support and coping strategies.

          Conclusion:

          This study confirmed that parents of children with ASD carry a huge caregiving burden, and added to our understanding of the factors associated with burden. The findings may help inform the design of effective interventions aimed at reducing burden among the parents of children with ASD.

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          Most cited references144

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          The Multidimensional Scale of Perceived Social Support

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            You want to measure coping but your protocol's too long: consider the brief COPE.

            Studies of coping in applied settings often confront the need to minimize time demands on participants. The problem of participant response burden is exacerbated further by the fact that these studies typically are designed to test multiple hypotheses with the same sample, a strategy that entails the use of many time-consuming measures. Such research would benefit from a brief measure of coping assessing several responses known to be relevant to effective and ineffective coping. This article presents such a brief form of a previously published measure called the COPE inventory (Carver, Scheier, & Weintraub, 1989), which has proven to be useful in health-related research. The Brief COPE omits two scales of the full COPE, reduces others to two items per scale, and adds one scale. Psychometric properties of the Brief COPE are reported, derived from a sample of adults participating in a study of the process of recovery after Hurricane Andrew.
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              Assessing coping strategies: A theoretically based approach.

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                Author and article information

                Journal
                Clin Pract Epidemiol Ment Health
                Clin Pract Epidemiol Ment Health
                CPEMH
                Clinical Practice and Epidemiology in Mental Health : CP & EMH
                Bentham Open
                1745-0179
                31 July 2018
                2018
                : 14
                : 143-176
                Affiliations
                [1 ]Centre for Behavioural Sciences and Mental Health, Italian National Institute of Health, Rome. Italy
                [2 ]Department of Mental Health, Local Health Unit, Trento, Italy
                [3 ]Department of Pediatrics and Child and Adolescent Neuropsychiatry, Marche Nord Hospital, Fano, Italy
                [4 ]Child Neuropsychiatry Unit and Centre for Neurodevelopmental Disorders, Pescara, Italy
                [5 ]Neurological and Psychiatric Child Unit, Pediatric Department, Alessandria Hospital, Alessandria, Italy
                [6 ]Department of Psychology, Sapienza University of Rome, Italy
                [7 ]Women’s Health Unit, National Centre of Epidemiology Surveillance and Health Promotion, Italian National Institute of Health, Rome. Italy
                [8 ]Italian Society for Child and Adolescent Neuropsychiatry, Italy
                [9 ]Italian Autism Foundation, Rome, Italy
                Author notes
                [* ]Address correspondence to this author at the Centre for Behavioural Sciences and Mental Health, Italian National Institute of Health, Viale Regina Elena, 299 - 00161 Rome, Italy; Tel: +39 06 49904200; Fax: +39 06 49904182; E-mail: angelo.picardi@ 123456iss.it
                Article
                CPEMH-14-143
                10.2174/1745017901814010143
                6080067
                30158998
                d78b94a6-b931-4b63-a1e9-bf2ba025a89d
                © 2018 Picardi et al.

                This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: https://creativecommons.org/licenses/by/4.0/legalcode. This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 2 February 2018
                : 10 April 2018
                : 11 April 2018
                Categories
                Clinical Practice Epidemiology in Mental Health

                Neurology
                autism spectrum disorders,parental burden,psychological distress,coping,resilience,social support

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