Publication Date
| In 2025 | 0 |
| Since 2024 | 0 |
| Since 2021 (last 5 years) | 0 |
| Since 2016 (last 10 years) | 0 |
| Since 2006 (last 20 years) | 1 |
Descriptor
| Access to Health Care | 1 |
| Adults | 1 |
| At Risk Persons | 1 |
| Correlation | 1 |
| Decision Making | 1 |
| Epilepsy | 1 |
| Foreign Countries | 1 |
| Health Services | 1 |
| Informed Consent | 1 |
| Interviews | 1 |
| Mental Retardation | 1 |
| More ▼ | |
Source
| Journal of Intellectual… | 1 |
Publication Type
| Journal Articles | 1 |
| Reports - Research | 1 |
Education Level
Audience
Location
| United Kingdom (England) | 1 |
Laws, Policies, & Programs
Assessments and Surveys
What Works Clearinghouse Rating
Peer reviewed
Direct linkRedley, M.; Prince, E.; Bateman, N.; Pennington, M.; Wood, N.; Croudace, T.; Ring, H. – Journal of Intellectual Disability Research, 2013
Background: Patients with intellectual disabilities (ID) receive health care by proxy. It is family members and/or paid support staff who must recognise health problems, communicate with clinicians, and report the benefits, if any, of a particular treatment. At the same time international and national statutes protect and promote the right of…
Descriptors: Parent Participation, Decision Making, Health Services, Mental Retardation
