Linked from

The 177 pages that link to Informed consent, each with the reason it gives.

• Genetic counselingRelated: Counseling supports a considered choice about testing rather than treating testing as automatic.

• PsychotherapyRelated: Psychotherapy requires clear agreement about goals, methods, confidentiality, and foreseeable risks.

• Oral historyRelated: Interviewees need to understand how their testimony may be recorded, preserved, and shared.

• Clinical trialRelated: Participants must understand the study before agreeing to join.

• Placebo effectRelated: Deceptive placebo use collides with it; open-label placebo partially resolves the clash.

• Exposure therapyRelated: Exposure requires clear agreement about exercises, risks, and the treatment rationale.

• Trauma-informed careRelated: Meaningful choice requires clear information and the ability to decline or pause care.

• Prenatal diagnosisRelated: Prenatal testing should be chosen with an understanding of its limits and possible consequences.

• Sexual consentRelated: Information about the activity and relevant conditions shapes meaningful agreement.

• Newborn screeningRelated: Programs differ on how parents are informed about screening and optional tests.

• Shared decision-makingRelated: Shared decisions support consent, while informed consent also addresses authorization and disclosure duties.

• PseudoscienceRelated: Patients need clear disclosure when pseudoscientific treatments are offered as established medical care.

• Language documentationRelated: Consent practices determine what may be recorded, archived, shared, or restricted.

• Participant observationRelated: Ongoing relationships in field settings complicate how consent is requested and maintained.

• Research ethicsRelated: It makes participation a choice grounded in understandable information about a study.

• AutonomyRelated: It puts decision-making authority into practice in medicine and research.

• OverdiagnosisRelated: Consent for screening is more meaningful when it includes the possibility of overdiagnosis.

• Risk communicationRelated: Risk disclosure is central when people decide whether to accept health interventions.

• Physical examinationRelated: Patients must be able to understand and agree to examination, especially intimate or sensitive maneuvers.

• DeontologyRelated: It expresses respect for persons by limiting what may be done without their authorization.

• Reproductive rightsRelated: Reproductive health care depends on patients choosing among procedures and treatments without coercion.

• Deep brain stimulationRelated: DBS requires weighing uncertain benefits, irreversible surgery, and ongoing device management.

• PlaceboRelated: Placebo use in care must be considered alongside disclosure and patient autonomy.

• Fiduciary dutyRelated: Disclosure and consent can sometimes authorize conduct that would otherwise breach loyalty.

• Kantian ethicsRelated: Respecting rational agency gives a Kantian basis for requiring genuine consent.

• Field experimentRelated: Field interventions must address consent when people are directly recruited or affected.

• Preimplantation genetic testingRelated: Patients need to understand uncertainty and possible outcomes before testing embryos.

• Qualitative researchRelated: It is especially consequential when researchers build relationships through ongoing fieldwork.

• BioethicsRelated: It turns respect for autonomy into a practical requirement in care and research.

• Genetic privacyRelated: Consent defines which genetic tests, data uses, and disclosures a person authorizes.

• IntersexRelated: It is central to disputes about deferrable interventions on intersex children.

• Plain languageRelated: Consent is meaningful only when the information can be understood.

• Data privacyRelated: Consent is one common basis for collecting or using personal information.

• Electroconvulsive therapyRelated: ECT requires discussion of expected benefits, risks, alternatives, and the person’s decision-making rights.

• Health literacyRelated: Understanding risks and choices is necessary for meaningful consent.

• Medical model of disabilityRelated: Treatment-centered approaches raise questions about who controls decisions involving disabled bodies.

• Clinical interviewRelated: Explaining the interview's purpose and limits supports voluntary participation.

• First aidRelated: When a person is conscious and able to decide, permission generally precedes care.

• Gender-affirming careRelated: Consent supports decisions about interventions by clarifying benefits, risks, and alternatives.

• Mass drug administrationRelated: Public-health scale does not remove the need to explain treatment and respect voluntary choice.

• TelemedicineRelated: Patients may need to understand the limits, privacy risks, and alternatives of remote care.

• Conversion therapyRelated: Consent is compromised when clients are misled about efficacy or pressured to change.

• Prenatal screeningRelated: Screening choices require understanding what results can and cannot establish.

• ThalidomideRelated: The crisis sharpened scrutiny of how patients are told about uncertain drug risks.

• Embryonic stem cellRelated: Donors must consent to the use of embryos or reproductive material in research.

• Female genital mutilationRelated: Girls cannot provide adult consent, while adult requests require careful, noncoercive assessment.

• Psychological assessmentRelated: Assessment requires clear explanation of its purpose, procedures, and intended use.

• SexologyRelated: Research on intimate topics requires clear, voluntary consent and privacy safeguards.

• Supported decision-makingRelated: Chosen assistance can make information accessible while leaving consent with the person.

• Health communicationRelated: It depends on communication that makes risks, benefits, and alternatives understandable.