Children with intellectual disability (ID) frequently have significant educational, social and health care needs, resulting in caregivers often experiencing a wide range of negative effects. This paper aims to determine the impact of childhood ID on caregivers’ health‐related quality of life (HRQoL) across co‐morbid diagnostic groups. The second aim of this study is to determine the risk factors associated with lower HRQoL in this population.
Visit (off-site)- Author:
- UTS Centre for Health Economics Research and Evaluation
- Source:
- Journal for Intellectual Disability Research
- Date published:
- Sun 15th Dec, 2019