Individual support planning: perceptions and expectations of people with intellectual disabilities in the Netherlands
Version of Record online: 14 SEP 2012
© 2012 The Authors. Journal of Intellectual Disability Research © 2012 John Wiley & Sons Ltd, MENCAP & IASSID
Journal of Intellectual Disability Research
Volume 57, Issue 11, pages 1027–1036, November 2013
How to Cite
Herps, M. A., Buntinx, W. H. E. and Curfs, L. M. G. (2013), Individual support planning: perceptions and expectations of people with intellectual disabilities in the Netherlands. Journal of Intellectual Disability Research, 57: 1027–1036. doi: 10.1111/j.1365-2788.2012.01598.x
- Issue online: 23 SEP 2013
- Version of Record online: 14 SEP 2012
- Accepted 26 June 2012
- individual support planning;
- intellectual disabilities;
- service-user perspective
Background According to Dutch jurisdiction, individual support plans (ISP) should register the mutual agreements between a person with intellectual disabilities (ID) and a professional service organisation with respect to the support that will be provided. In planning for support, active involvement of both parties is necessary. The current study focuses on the perceptions and experiences of Dutch persons with ID with respect to their involvement in their ISP.
Method Data were gathered through semi-structured interviews with 61 people with mild to moderate ID. Participants were recruited in 23 Dutch service provider organisations. A systematic qualitative analysis was performed on the interview transcripts.
Results Although persons with ID are present at their ISP meeting, active client involvement in developing, executing and evaluating the ISP is not common practice. Issues of accessibility and lack of control over the process and content of ISP hamper effective involvement of people with ID.
Conclusions The study raises questions concerning ISP practices in the Netherlands. The question needs to be addressed as to how to facilitate active involvement of people with ID in planning for support. The results further suggest that support organisations perceive an ISP rather as a formal document to comply with bureaucratic rules than as an instrument of empowerment to enhance control of persons with ID over their own lives.