informed consent in research (Prof. Oamr Kasule)


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informed consent in research (Prof. Oamr Kasule)

  1. 1. CONSENT BY SUBJECT FORPARTICIPATION IN RESEARCH Prof Omar Hasan Kasule Department of Bioethics Lecture for 4th year medical students 7th May 2012
  2. 2. INFORMED CONSENT TEMPLATE INSTRUCTIONS Final consent must be in 12 pt, as are sample text in this template The investigator should fill in the appropriate information. Some places have example text that must be replaced This template is intended to be used electronically. If so, be sure to delete everything that doesn’t belong This template is an attempt to be comprehensive, to facilitate preparing ICDs (Informed Consent Documents) for all occasions.
  3. 3. PROJECT IDENTIFICATION INFORMATION Protocol Number: Study Title: Name of Subject: Medical Record Number: Principal Investigator Address: Telephone:
  4. 4. INTRODUCTORY REMARKS A member of the research team will explain what is involved in this study and how it will affect you. This consent form describes the study procedures, the risks and benefits of participation, and how your confidentiality will be maintained. Please take your time to ask questions and feel comfortable making a decision whether to participate or not. This process is called informed consent. If you decide to participate in this study, you will be asked to sign this form and will be given a copy for your records. Throughout this consent form, “you” will refer to you or your child, as appropriate.
  5. 5. WHY IS THIS STUDY BEING DONE? To investigate the effects of Sildenafil (Viagra) on the parameters of the pulmonary function test in Asthma patients who have been prescribed the drug for erectile dysfunction treatment. The study is funded by KFMC
  6. 6. HOW MANY PEOPLE WILL TAKEPART IN THE STUDY? 80 Male Patients All recruited at KFMC Saudi and non-Saudi
  7. 7. WHAT WILL HAPPEN IF I TAKEPART IN THIS STUDY? A pulmonary function test will be performed on you once before and once two-hours after intake of Sildenafil (50mg) orally weekly Test will be repeated for 6 weeks during your routine doctor visits to Urology Clinic at KFMC.
  8. 8. STUDY LOCATION: KFMC, MAIN HOSPITAL Pulmonology Department Spirometry Lab
  9. 9. WHAT IS EXPECTED OF MEDURING THE STUDY? Attend the clinic for the duration of the study which is 6 consecutive weeks Take the medication Undergo the spirometry test
  10. 10. CAN I STOP BEING IN THE STUDY? You can decide to stop at any time. Tell the study doctor if you are thinking about stopping or you’ve decided to stop. He or she will tell you how to stop your participation safely. No one will try to get you to change your mind. There are no risks associated with stopping being in the study
  11. 11. WHAT SIDE EFFECTS OR RISKS CAN IEXPECT FROM BEING IN THE STUDY? Waiting for 2 hours in the hospital after oral intake of 50 mg Sildenafil Slight headache might occur Slight blurred vision might occur Minor discomfort of undergoing the spirometery for a few minutes
  12. 12. ARE THERE BENEFITS TOTAKING PART IN THE STUDY? We hope the results would give a positive indications to establish the drug for the treatment of asthma Taking part in this study may or may not make your health better. The doctors hope the drug will be more effective / have fewer side effects than the standard (usual) treatment, there is no proof of this yet.
  13. 13. WHAT OTHER OPTIONS ARETHERE? No other options are available
  14. 14. WHAT HAPPENS IF I AM INJURED BECAUSE I TOOK PART IN THIS STUDY? It is important that you tell Dr. …. if you feel that you have been injured because of taking part in this study. You can tell the doctor in person or call him atxxxxxx. If you are injured as a result of being in this study, treatment will be available. The costs of the treatment may be covered by KFMC or the study sponsor, depending on a number of factors. KFMC and the study sponsor do not normally provide any other form of compensation for injury. For further information about this, you may call the office of the Institutional Review Board (IRB) at 288- 9999 ext 8391 or 1299.
  15. 15. 15.0 WHAT ARE THE COSTS OF TAKING PART IN THE STUDY?You will not be charged for any study activities.
  16. 16. WILL I BE PAID FOR MY TAKINGPART IN THIS STUDY? In return for your time, effort and travel expenses, you will be paid taking part in this study. You will be paid xxx SR for participating each week. Since the study is 6-weeks, you will be paid a total of xxxSR for the entire duration of the study.
  17. 17. WILL MY MEDICAL INFORMATIONBE KEPT PRIVATE? We will do our best to make sure that the personal information in your medical record is kept private. However, we cannot guarantee total privacy. Your personal information may be given out if required by law. If information from this study is published or presented at scientific meetings, your name and other personal information will not be used.
  18. 18. WHAT ARE MY RIGHTS IF I TAKE PART IN THISSTUDY?  Taking part in this study is your choice. You may choose either to take part or not to take part in the study. If you decide to take part in this study, you may leave the study at any time.  No matter what decision you make, there will be no penalty to you and you will not lose any of your regular benefits.  Leaving the study will not affect your medical care. You can still get your medical care from KFMC.  We may use information that was collected prior to your leaving the study.  We will tell you about new information or changes in the study that may affect your health or your willingness to continue in the study.  In the case of injury resulting from this study, you do not lose any of your legal rights to seek payment by signing this form. 
  19. 19. WHO DO I CALL IF I HAVEQUESTIONS OR PROBLEMS? Before you agree to be in this study, you will talk to a study team member qualified to tell you about this study. You can ask questions about any aspect of the research. If you have further questions about the study, you may ask them at any time. You may call xxxxxxx
  20. 20. SIGNATURE BY THE SUBJECT The research and procedures have been explained to me. I have been allowed to ask any questions I have at this time. I can ask any additional questions I may think of later. I may quit being in the study at any time without affecting my health care. I will receive a signed copy of this consent form.I agree to participate in this study. My agreement is voluntary. I do not have to sign this form if I do not want to be part of this research study.Subject Signature Date Place Time (AM PM )
  21. 21. SIGNATURE BY PERSONOBTAINING CONSENT have explained the nature and purpose of the study and the risks involved. I have answered and will answer questions to the best of my ability. I will give a signed copy of the consent form to the subject. Signature of Person Obtaining Consent Date Place Time (AM PM )
  22. 22. SIGNATURE BY PRINCIPALINVESTIGATOR Signature of Principal Investigator Place Date Time (AM PM )