What is proxy informed consent?
Informed consent for surgical procedures requires that the procedures are explained and that the patient understands the procedures and risks and agrees to undergo them. Proxy consent occurs when an individual is provided with the legal right to make decisions on behalf of another.
What are the three types of informed consent?
Valid informed consent for research must include three major elements: (1) disclosure of information, (2) competency of the patient (or surrogate) to make a decision, and (3) voluntary nature of the decision.
What is proxy consent and who are legally acceptable representatives?
Proxy consent is the process by which people with the legal right to consent to medical treatment for themselves or for a minor or a ward delegate that right to another person.
Who can give proxy consent?
If an individual is personally unable to consent to a medical intervention on account of their age or lack of intellectual maturity, the proxy consent of a legal representative is required. In this context the legal representative is bound by the well-being of the person on behalf of whom consent is given.
What are the types of informed consent in research?
Signed/written consent. Signed, written consent form prior to participation.
What are the 6 elements of informed consent?
B. Basic Elements of Informed Consent
- Description of Clinical Investigation.
- Risks and Discomforts.
- Benefits.
- Alternative Procedures or Treatments.
- Confidentiality.
- Compensation and Medical Treatment in Event of Injury.
- Contacts.
- Voluntary Participation.
What should be included in informed consent in research?
Describe, in sequence, what will happen in the course of the research, giving enough detail for the participant to gain a clear idea of what to expect. Explain the nature, likelihood and treatment of anticipated risks, discomfort or adverse effects, including psychological and social risks, if any.