Informed consent

Informed consent — is a decision to participate in examination/assessment, intervention/treatment or research, taken by a competent individual who has received the necessary information; who has adequately understood the information; and who, after considering the information, has arrived at a decision without having been subjected to coercion, undue influence or inducement, or intimidation. Informed consent is based on the principle that competent individuals are entitled to choose freely whether to participate in examination/assessment, intervention/treatment or research. Informed consent protects the individual's freedom of choice and respects the individual's autonomy. [1]

In order to obtain the valid consent of patients for assessment, treatment or participation in research, they must be informed of all potential and significant risks, benefits and likely outcomes of treatment, taking into account their age, emotional state and cognitive ability, to allow valid/informed consent to be given. [2]

References

Council of International Organizations of Medical Science. Ethical Guidelines for Biomedical Research Involving Human Subjects. London, UK: CIOMS; 2002. http://cioms.ch/publications/layout_guide2002.pdf (Access date 10th March 2017)

Chartered Society of Physiotherapy. Quality Assurance Standards for physiotherapy service delivery. London, UK.: CSP; 2013. http://www.csp.org.uk/publications/qualityassurance-standards (Access date 10th March 2017)

European Region of World Confederation for Physical Therapy. European Core Standards of Physiotherapy Practice. Brussels, Belgium: ER-WCPT; 2008.  http://www.physio-europe.org/download.php?document=71&downloadarea=6 (Access
date 22nd March 2010)