Does the consumer need to sign an informed consent prior to completing the SAVR-S?
• Current use of the SAVR-S by VR programs is a clinical, not research activity. It does not differ from any other clinical screening that VR may use, contract for, or purchase. • The state VR programs currently using the SAVR-S have agreed to conduct an evaluation of how the SAVR-S assists counselors in case planning and also whether it can positively impact successful closures. This activity is a clinical service evaluation, and it is exempted from human subjects “research”. • The evaluation of this screening process using de-identified SAVR-S data has been reviewed and approved as an exempted activity by the Human Subjects Committees at Wright State and Northwestern Universities. The eventual goal of this field trial is to develop multiple administration formats that are easy for counselors to administer.
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