informed consent

USAGE SUMMARY

The phrase "informed consent" is correct and usable in written English.
It is used in a legal context to refer to the agreement of a patient to receive medical treatment after being made fully aware of the risks and benefits of the treatment. For example: Before the surgery, the patient signed an informed consent form that outlined the potential risks and benefits of the procedure.

✓ Grammatically correct

Science

Academia

News & Media

Human-verified examples from authoritative sources

Exact Expressions

60 human-written examples

Informed consent: There are new required elements of informed consent.

Duke University

Can't sled without informed consent".

The New Yorker

All patients provided informed consent.

Nature

Informed consent and ethical equivocations.

Nature

So much for informed consent.

The Guardian

An informed consent was obtained.

Nature

Participation was by informed consent.

Nature

Participants gave written informed consent.

Nature

Informed consent or legalized rape?

The New York Times

Autonomy, informed consent, and psychosurgery.

Harvard University

Informed Consent and Ethical Equivocations.

Harvard University

Expert writing Tips

Best practice

When documenting "informed consent", be specific about what information was conveyed, how it was conveyed, and ensure you have documented evidence that the patient or participant understood the information.

Common error

Do not assume that a signed consent form automatically means "informed consent" was obtained. Always verify the individual's understanding through direct questioning and provide opportunities for clarification.

Linguistic Context

The phrase "informed consent" functions as a noun phrase, typically serving as the subject or object of a sentence. It denotes a legal and ethical principle related to autonomy and decision-making. Ludwig AI highlights its common use across various contexts.

Expression frequency: Very common

Frequent in

Science

48%

Academia

22%

News & Media

17%

Less common in

Formal & Business

7%

Wiki

3%

Encyclopedias

0%

Ludwig's WRAP-UP

In summary, "informed consent" is a crucial noun phrase with legal and ethical implications. Ludwig AI confirms its correctness and usability, noting its prevalence across science, academia, and news media. It signifies that permission has been granted based on full knowledge and understanding. When using this phrase, ensure you focus on conveying both the "informed" and "consent" aspects, documenting the process thoroughly to avoid assumptions. Alternatives like "voluntary agreement" or "explicit consent" can be used depending on the specific nuance you want to convey.

More alternative expressions

Phrases that express similar concepts, ordered by semantic similarity:

explicit consent

Highlights the clear and unambiguous nature of the consent.

affirmative consent

Focuses on the active and positive nature of the consent given.

educated permission

Implies that the person giving permission has been informed and understands the implications.

conscious approval

Stresses the deliberate and aware nature of the approval given.

knowing authorization

Highlights the element of awareness and knowledge in granting permission.

agreement with awareness

Highlights that agreement is given with a full understanding of the relevant information.

voluntary agreement

Focuses on the voluntary aspect, emphasizing the freedom of choice in consenting.

permission with knowledge

Emphasizes that permission is granted based on a foundation of knowledge.

understanding assent

Emphasizes comprehension and agreement, particularly in situations involving individuals with limited capacity to consent.

voluntary participation

Shifts the focus to the voluntary nature of involvement, implying consent.

FAQs

What does "informed consent" mean?

"Informed consent" refers to the process where a person, before agreeing to a medical procedure, research study, or other intervention, is provided with all relevant information, including potential risks and benefits, and gives their agreement freely.

What are the key elements of "informed consent"?

The key elements include providing sufficient information, ensuring the individual understands the information, obtaining voluntary agreement, and documenting the process.

When is "informed consent" required?

"Informed consent" is typically required for medical treatments, research studies involving human subjects, and any situation where an individual's autonomy and right to make decisions about their body or health are involved.

What happens if "informed consent" is not obtained?

Failure to obtain "informed consent" can have legal and ethical consequences, potentially leading to claims of negligence, battery, or violation of ethical principles.