Abstract
This paper describes the experiences of a researcher negotiating consent with people with learning disabilities to become participants in a research study. The study was about how the Mental Capacity Act (MCA) was applied to everyday decision making in social care settings. However, before data collection could begin, the researcher had to follow the principles of the MCA and the requirements of ethical research practice. The paper reports on the important role of gatekeepers in allowing (or preventing) access to potential participants. However, gatekeepers did not always act in a manner in keeping with the first principle of the MCA. Additionally, the dilemmas for a researcher in assessing participants’ capacity to consent to the study are described, as are three approaches followed which supported people to decide for themselves.
| Original language | English |
|---|---|
| Pages (from-to) | 128-134 |
| Number of pages | 7 |
| Journal | British Journal of Learning Disabilities |
| Volume | 43 |
| Issue number | 2 |
| Early online date | 18 May 2015 |
| DOIs | |
| Publication status | Published - Jun 2015 |
Keywords
- Mental Capacity Act,
- Learning Disabilities
- research ethics,
Fingerprint
Dive into the research topics of 'Applying the Mental Capacity Act to research with people with learning disabilities'. Together they form a unique fingerprint.Profiles
-
Dr Marcus Jepson
- Applied Health Research - Associate Professor in Qualitative Health Science
- Bristol Population Health Science Institute
Person: Academic , Member
Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver