That is the typical approach used here. But, it does necessitate having a code number associated with the data. In very sensitive situations, alternatives, such as the one I suggested earlier, have been used. I'll be interested in what others have to say. Sally Martin ----- Original Message ----- From: Little, Christina <Little.Christina@xxxxxxxxxx> To: Child Maltreatment Researchers <CHILD-MALTREATMENT-RESEARCH-L@xxxxxxxxxxx> Sent: Monday, January 22, 2001 9:45 AM Subject: RE: Informed Consent > In my experience, consent forms or any other document that has the subjects' > name or identifying information on it, are always kept separate from the > other data so that they cannot be matched. One person, such as the primary > investigator or study coordinator keeps a confidential list with the matched > information in a separate place from either consents or the data. I'd be > interested to know if anyone does anything different. > > -----Original Message----- > From: Ron Kokish [mailto:dka@xxxxxxxxxxxxxx] > Sent: Monday, January 22, 2001 10:04 AM > To: Child Maltreatment Researchers > Subject: RE: Informed Consent > > > Thank you for your reply. My question may have been unclear. I'm inquiring > about informed consent for research using an anonymous questionnaire ABOUT > polygraph examinations, not informed consent for polygraph examinations > themselves. I'm doing this research because polygraph use is becoming > increasingly common in sex offender management and treatment and, as you > said, "reliability, as regards interpretation, . . .is highly questionable." > I'm hoping to shed a bit of light on this very question. > > > . . .>>I plan to have them (the participants) submit their questionnaires > anonymously. This means that, while I will have them complete informed > consent forms, I will be unable to tie the consent form to a particular > questionnaire. Is this acceptable? If not, how does one resolve the > anonymity problem?<< > > In other words, since an anonymous questionnaire can't, by design, be tied > to a name, the consent forms have to be kept separated from the research > instrument. How then, does one assure ethics committees that each > participant did in fact sign a consent form. I'm sure there's a simple > approach to this, but being a research novice, I'm unaware of it. > > **************************************************************************** > *** > Ron Kokish at Delson-Kokish Associates, P.O. Box 476, Trinidad, CA 95570 > Clinical and Forensic Consultation and Training for Agencies and Courts > (707)677-3181 (voice) ron@xxxxxxxxx (Email) (707) 677-0187 (fax) > ****** On the World Wide Web @ www.northcoast.com/~dka ****** > > > > -----Original Message----- > From: Michael A. Fraga, Psy.D., DABFE [mailto:MichaelSan@xxxxxxxxxxxxx] > Sent: Monday, January 22, 2001 8:43 AM > To: dka@xxxxxxxxxxxxxx > Subject: Re: Informed Consent > > > A similar use of the polygraph (with so's) has been used in Sonoma County. > As the measure is not admissible in a court of law, and has as yet to be > proven to accomplish what it purports to do with any statistical degree of > inter-rater (in this case operator) reliability, as regards interpretation, > its use is highly questionable clinically except as a coercive aspect of > supervision which is the manner currently being employed here. As for the > root question, 'standardized' questionnaires, both written, and the verbally > delivered format utilize the administration of the polygraph; structure as > in content would seem to be the issue, questions would best be served if > they were generic to either the offense category, or the aspects of > supervision in the code. > > > Michael A. Fraga, Psy.D. > Ananda Institute > Family Trauma Research and Treatment > Santa Rosa, CA >
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