{"entity":{"id":"informed-consent","kind":"term","name":"Informed consent","aka":["informed consent","consent form","consent forms","participant information sheet","patient information sheet","informed consent form","ICF","consent process","consenting","consented","gave written informed consent","written informed consent","signed consent","withdraw consent","withdrawal of consent","withdrew consent","right to withdraw","assent","parental permission","broad consent","re-consent","reconsent","optional consent","consent for future research","biobank consent","tissue consent","waiver of consent","deferred consent","legally authorised representative","capacity to consent"],"tldr":"Informed consent is the conversation and the signed form in which a person learns what a trial involves, what might go wrong, what the alternatives are and that they can leave at any time, and then freely agrees to take part.","summary":"Consent to a trial is a process, not a signature. The investigator or a trained member of the team explains the purpose of the study, what it will involve beyond normal care (extra visits, biopsies, scans, questionnaires), the known and possible risks, the possible benefits including the honest statement that there may be none for the individual, the alternatives including standard treatment outside the trial, how data and samples will be used and protected, who is paying and who to contact, and the right to withdraw at any time without losing care. The participant information sheet sets this out in plain language and the person has time to read it, ask questions and discuss it with family before signing. Consent is documented again when the protocol changes materially (re-consent) and is sought separately for optional elements such as tissue banking, genetic testing or future research. Children give assent while a parent gives permission, and adults who cannot consent for themselves are enrolled only through a legally authorised representative and only when the research could not be done in others.\n\nSeveral trial designs stretch the standard model. Cluster-randomised trials such as the Kerala, Mumbai and Osmanabad screening trials randomise communities, so consent to randomisation sits with community or institutional gatekeepers while individuals consent to screening and to data use. Registry-based and trial-within-a-cohort designs seek broad consent up front for future randomisation. Decentralised trials use electronic consent by video, which regulators accept when identity, comprehension and documentation are assured. Emergency research uses deferred consent. In every case the ethics committee reviews the consent materials, and regulators inspect the signed forms.\n\nThe persistent problems are comprehension and coercion. Consent forms have grown to dozens of pages of legal language that few participants read; readability studies routinely find them written above the reading level of most patients, which is why the pattern of a short summary followed by detail is now required in the United States. The therapeutic misconception, joining a trial in the belief that the experimental arm must be better, undermines the voluntariness that consent is meant to protect, and people facing a life-threatening diagnosis with no other options are, by any definition, under pressure. Good consent names that pressure rather than pretending it away.","asOf":"2026-09-17","wikipedia":"https://en.wikipedia.org/wiki/Informed_consent","links":[{"label":"Wikipedia","url":"https://en.wikipedia.org/wiki/Informed_consent"},{"label":"FDA guidance: informed consent for IRBs, clinical investigators and sponsors","url":"https://www.fda.gov/regulatory-information/search-fda-guidance-documents/informed-consent"},{"label":"WMA Declaration of Helsinki","url":"https://www.wma.net/what-we-do/medical-ethics/declaration-of-helsinki/"}],"tags":[],"related":["ethics-review","clinical-equipoise","accrual","decentralised-trial","cluster-randomised-trial","registry-based-trial","trial-lifecycle","clinical-trial"],"cancers":[],"sections":["drug-discovery"],"technologies":[],"targets":[],"drugs":[],"companies":[],"institutions":[],"pathways":[],"terms":[],"trials":["kerala-oral-screening","add-aspirin"],"people":[],"bottlenecks":["b-trial-diversity","b-trial-enrolment"],"keyPapers":[],"journals":[],"dependsOn":[],"notes":[],"category":"Trials"},"route":"/terms/informed-consent/","neighbours":{"term":[{"id":"accrual","kind":"term","name":"Accrual and enrolment","route":"/terms/accrual/"},{"id":"clinical-equipoise","kind":"term","name":"Clinical equipoise","route":"/terms/clinical-equipoise/"},{"id":"clinical-trial","kind":"term","name":"Clinical trial","route":"/terms/clinical-trial/"},{"id":"cluster-randomised-trial","kind":"term","name":"Cluster-randomised trial","route":"/terms/cluster-randomised-trial/"},{"id":"decentralised-trial","kind":"term","name":"Decentralised trial","route":"/terms/decentralised-trial/"},{"id":"ethics-review","kind":"term","name":"Ethics review (IRB, research ethics committee)","route":"/terms/ethics-review/"},{"id":"first-in-human","kind":"term","name":"First-in-human (FIH) trial","route":"/terms/first-in-human/"},{"id":"trial-phases","kind":"term","name":"Phase 1, 2 and 3 trials","route":"/terms/trial-phases/"},{"id":"placebo","kind":"term","name":"Placebo","route":"/terms/placebo/"},{"id":"registry-based-trial","kind":"term","name":"Registry-based randomised trial","route":"/terms/registry-based-trial/"},{"id":"trial-lifecycle","kind":"term","name":"Trial lifecycle: from protocol to label","route":"/terms/trial-lifecycle/"}],"section":[{"id":"drug-discovery","kind":"section","name":"Drug Discovery Platforms","route":"/fronts/drug-discovery/"}],"trial":[{"id":"add-aspirin","kind":"trial","name":"Add-Aspirin","route":"/trials/add-aspirin/"},{"id":"kerala-oral-screening","kind":"trial","name":"Kerala oral cancer visual screening trial (Trivandrum)","route":"/trials/kerala-oral-screening/"}],"bottleneck":[{"id":"b-trial-diversity","kind":"bottleneck","name":"Trials do not represent the people who get cancer","route":"/bottlenecks/b-trial-diversity/"},{"id":"b-trial-enrolment","kind":"bottleneck","name":"Trials enrol too few, too slowly","route":"/bottlenecks/b-trial-enrolment/"}]}}