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How does ECT work?
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FDA believes that translation of the long form is critically important as a means of providing subjects an ongoing source of information understandable to them.
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The investigators should also provide the IRB with a description of how interpreters for oral communication will be made available to subjects during the research.
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History and Mental Status Examination Overview Patient.
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This requirement will usually be met by having the informed consent.
To diminish confusion about the change, the investigator may use a prepared summary of the change to aid in an informative presentation to the enrolled subject.
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George undergoes an ECT treatment to deal with his increasing paranoia.
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FDA recommends that a copy of the signed consent form be provided.
CONSENT TO ACT AS A PARTICIPANT IN A RESEARCH STUDY Key Element 3 Who is.
HIV and sexually transmitted diseases, emergency contraception, pregnancy testing and counseling, treatment for any other injuries, rape crisis counseling, referrals for additional services and the collection of forensic evidence.
ECT involves multiple administrations, typically given two or three times per week until the patient is no longer suffering symptoms.
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