Table of ContentsInformed Consent and the RAC Appendix M-III Is Very Good Guidance Proposed Additional Consent Form Guidance The Context of Consent to GTR Gene Transfer Research: Consent/Communication Issues Consent and Subject Selection The Three Types of Benefit The Three Dimensions of Benefit Trial Phases and Consent Information Consent Forms May Inadvertently Convey Mixed Messages Purpose: It has been explained to you that you have nonsmall cell lung cancer that requires radiation therapy to the chest to relieve symptoms. You have been invited to participate in this research study. This study involves treatment with an experimental agent called Adenovirus CMV-p53 which is a modified common virus designed to carry a normal copy of the tumor suppressor gene p53 into tumor cells. Tumor cells are often killed or their growth is suppressed when this gene is put into them, and the hope is that we can improve your symptoms and prolong your life with this treatment. Adenovirus CMV-p53 will be given to you by bronchoscopy or percutaneously (through the skin) to a portion of your lung affected by your tumor. The purpose of this study is to determine whether this procedure is safe and to evaluate the effect of this treatment on your lung cancer. Benefits: It is not possible to predict whether or not any personal benefit will result. You have been told that, should your disease become worse, should side effects become very severe, should new scientific developments occur that indicate the treatment is not in your best interest, or should your physician feel that this treatment is no longer in your best interest, the treatment would be stopped. Purpose and Benefit A Good Benefits Section A Range of Benefit-Related Language Occasionally Seen A Rare Inclusion An Effort to Explain The Social Construction of Benefit in Gene Transfer Research What We’re Doing Consent Form Analysis IRB Interviews GTR Study Participant Interviews GTR Study Variables Possible Variables Consent Form Assessment Topics Comparing Direct Benefit in PS and CF, Surrogate and Clinical Endpoints Analysis Activities |
Author: Nancy M. P. King
Home Page: www.webconferences.com/nihoba |