ࡱ> 796_ jbjbj .h1bh1b278Th|Z\\\\\\$u qqqFZqZqq _FF0,s! ds!s!Lqqs!B : ORAL CONSENT GUIDANCE For protocols involving oral consent, following the HYPERLINK "http://www.davidson.edu/Documents/Administrative%20Department/Grants%20and%20Contracts/Human%20Subject%20IRB/Sample%20Adult%20Consent%20Form-91ɬ-College.doc"  Sample Consent Form to Participate in Research may not be practical or appropriate for assuring informed consent. A shorter, more conversational consent script may be appropriate. In such cases, the following information, at a minimum, must be communicated to the participant: Introductionintroduce yourself as the caller/interviewer, affiliation, organization Statement that the study involves research Study purpose Any risks or benefits associated with participating (leave this out if there are none) Any compensation, and any information that you will need to collect in order to make that payment (mailing address, email address, etc.) What will participant be asked to doas well as, the amount of time the participant will spend (include any follow-ups you plan to do) The voluntary nature of participation in the study, including the right to refuse or withdraw That you will be taking notes or recording the data Whether the information collected will remain confidential or if you plan to keep identifiers with the research data (e.g. if address is collected, will that be kept separate from the survey responses). Provide contact information for the researcher and/or the IRB providing oversight Ask if the participant has any questions that you can answer Ask explicitlydo you agree to participate in this research? Record the response. Depending on the nature of the study and the participant pool, the researcher may offer other pertinent information to assure that the participants are fully informed about the study and any risks or benefits from participating in it.     Source: Cornell University IRB Website IJ* +  : e   G1235ƱӟrfVF>:hljhlUhkEhkE5CJOJQJaJhkEhkE6CJOJQJaJh (CJOJQJaJhkEh (CJOJQJaJhkEhkECJOJQJaJh (0J5CJOJQJaJ#hs hkE0J5CJOJQJaJ(jhs 5CJOJQJUaJhs 5CJOJQJaJ"jhs 5CJOJQJUaJhVw5CJOJQJaJhkE5CJOJQJaJ  h  f e G24578:;=>fg dgdPF & Fgd ( & FgdkE5689;<>ghijhkEhkE5CJOJQJaJh,A@hPFhljhlU ghij,1h/ =!"#$% DyK yK <http://www.davidson.edu/Documents/Administrative Department/Grants and Contracts/Human Subject IRB/Sample Adult Consent Form-Davidson-College.docyX;H,]ą'c s666666666vvvvvvvvv666666>6666666666666666666666666666666666666666666666666hH66666666666666666666666666666666666666666666666666666666666666666p62&6FVfv2(&6FVfv&6FVfv&6FVfv&6FVfv&6FVfv&6FVfv8XV~ 0@ 0@ 0@ 0@ 0@ 0@ 0@ 0@ 0@ 0@ 0@ 0@ 0@ 0@ OJPJQJ_HmH nH sH tH J`J Normal dCJ_HaJmH sH tH DA D Default Paragraph FontRiR 0 Table Normal4 l4a (k ( 0No List @@@ kE List Paragraph ^m$>> PF0HeaderdH$.. PF0 Header Char> @"> PF0FooterdH$.1. PF0 Footer Char6U`A6 s 0 Hyperlink >*B*phcPK![Content_Types].xmlN0EH-J@%ǎǢ|ș$زULTB l,3;rØJB+$G]7O٭Vc:E3v@P~Ds |w< j 66695j gj I*jXL# @0(  B S  ?24578:;=>hk24578:;=>hkI+:eff1kUJcY ^`OJQJo(^`OJQJ^Jo(o p^p`OJQJo( @ ^@ `OJQJo(^`OJQJ^Jo(o ^`OJQJo( ^`OJQJo(^`OJQJ^Jo(o P^P`OJQJo(U           (E,=,A@PF2os [Y3lVwkER24@j@UnknownG*Ax Times New Roman5Symbol3. *Cx Arial7.K@Candara7.@Calibri?= *Cx Courier New;WingdingsA$BCambria Math"h"KjG"KjG1#1#!r0$$KHP  $PkE2!xx Oral Consent Guidance4oral consent, guidance, template, human subjects IRBDavidson CollegeWinecoff, Beverly Oh+'0 ,@ \h   Oral Consent Guidance91ɬ8oral consent, guidance, template, human subjects IRB Normal.dotmWinecoff, Beverly2Microsoft Office Word@F#@ _@ _1՜.+,D՜.+,P  hp  91ɬ#$ Oral Consent Guidance Title 8@ _PID_HLINKSA\Ehttp://www.davidson.edu/Documents/Administrative Department/Grants and Contracts/Human Subject IRB/Sample Adult Consent Form-Davidson-College.doc  !"#$%'()*+,-/0123458Root Entry Fz_:Data  1Table!WordDocument.SummaryInformation(&DocumentSummaryInformation8.CompObjr  F Microsoft Word 97-2003 Document MSWordDocWord.Document.89q