Abstract
Purpose
This study aimed to investigate the quality of life of parents of a child with autism spectrum disorder in Quebec.
Methods
Seventy-seven participants completed a questionnaire with socio-biographic information and five self-assessed scales, to measure perceived stress, social support and control, coping strategies, and quality of life.
Results
Perception of their child’s autonomy level, of the severity of the disorder, of the family’s income, as well as changes in their professional or familial organization influenced parents’ quality of life. Perceiving their situation as a threat predicted poor quality of life, whereas satisfaction of social support predicted good quality of life. In addition, parents who used problem solving and support-seeking coping strategies had a better relationship with their child, whereas those who used more emotion-centered coping strategies struggled. Lastly, parents who felt they had the power to contribute to their child’s development were more satisfied and less disturbed.
Conclusions
Beyond the parents’ actual situation, our results underscore the importance of paying attention to their own perception of the situation in order to provide them with appropriate support.
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Acknowledgements
We would like to thank the private clinic specialized in ASD and the “Fédération Québécoise de l’Autisme” who helped us in the recruitment process, and the parents who took part in this study.
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This study was not funded.
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All procedures performed in the study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments. This study received the approval from the Institutional ethical committee for research with human beings (CIEREH) of the University of Quebec in Montreal, as well as from the Ethical committee of joint research for the Centre for rehabilitation in intellectual disability and pervasive developmental disorder (CRDITED).
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Informed consent was obtained from all individual participants included in the study. Participation was voluntary and participants received no financial compensation for taking part in the study.
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Cappe, É., Poirier, N., Sankey, C. et al. Quality of life of French Canadian parents raising a child with autism spectrum disorder and effects of psychosocial factors. Qual Life Res 27, 955–967 (2018). https://doi.org/10.1007/s11136-017-1757-4
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DOI: https://doi.org/10.1007/s11136-017-1757-4