informed consent process



Similar documents
Practical aspects of early phase oncology trials the oncologists view

LUNG CANCER CLINICAL TRIALS

1. Study title Is the title self explanatory to a layperson? If not, a simplified title should be included.

Study Participant Experiences

Institutional Review Board

A guide for the patient

[Informed Consent Form for ] Name the group of individuals for whom this consent is written. Explanation Example

National Cancer Institute

Medicals c i e n t i f i c study

Consent what you have a right to expect

A Guide to Clinical Trials

TAKING PART IN CANCER TREATMENT RESEARCH STUDIES

Frequently Asked Questions About Georgia Workers Compensation Ty Wilson Attorney At Law

Research Ethics Review Committee (WHO ERC)

Clinical Trials: Improving the Care of People Living With Cancer

Consent what you have a right to expect

RESEARCH SUBJECT INFORMATION AND CONSENT FORM

Pl"OtocolDirector: Iris Schrijver _ IRB Approval Date: _June IRE Expiration Date: June 19, 2007 _ STANFORD SAMPLE CONSENT FORM

Cancer Clinical Trials: The Basics

What are Clinical Trials?

CONSENT FORM 12/19/08

Consulting Agreement

WORLD MEDICAL ASSOCIATION DECLARATION OF HELSINKI Ethical Principles for Medical Research Involving Human Subjects

Family Caregiver s Guide to Hospice and Palliative Care

Clinical Trials: Questions and Answers

Professional Standards and Guidelines

Clinical Trials: What You Need to Know

INFORMED CONSENT FOR EGG DONORS PRACTITIONER S GUIDE TO USING THE MODEL FORM

Patient Handbook on Stem Cell Therapies

CLINICAL CLINICAL TRIALS. How Clinical Trials Work for Children

Miami University: Human Subjects Research General Research Application Guidance

Guide to Criminal procedure

Frequently Asked Questions

Applicant and Opponent Surveys 2007 Summary of Findings

Clinical Trials: What You Need to Know

Entering a Clinical Trial

Consent Form: Example 2 (DNA Sequencing)

Utah Advance Directive Form & Instructions

Clinical Trials. Clinical trials the basics

DRAFT GUIDELINES ON AUDIO-VISUAL RECORDING OF INFORMED CONSENT PROCESS IN CLINICAL TRIAL

Every resident. Bill of Rights for people who live in Ontario long-term care homes. September 2008

Clinical Trial Compensation Guidelines

Advisors Turning Independent Study. February 2012

When investigative sites are struggling with subject recruitment, and it

RESEARCH PARTICIPANT INFORMED CONSENT AND PRIVACY AUTHORIZATION FORM

Durable Power of Attorney For Finances

TOP 10 MOST COMMON MISTAKES MADE IN HANDLING YOUR OWN INJURY CLAIM

Case study 1 - Eileen, 69: A disagreement with a hospital doctor led to the doctor refusing to continue treatment.

Advance Health Care Directive Instructions

YOUR RIGHT TO MAKE HEALTH CARE DECISIONS

XARELTO: WHAT YOU NEED TO KNOW ABOUT IT

Patient Information Leaflet: Part 1 select-d

Nova Southeastern University IRB - Consent Form Checklist Version Date: 02/17/2010

If you are signing for a minor child, you refers to your child throughout the consent document.

Information for Patients. Advance Health Care Directive Kit A guide to help you express your health care wishes

Plan Member Privacy Information Package

Copyright 2013 wolfssl Inc. All rights reserved. 2

LEGALLY ADEQUATE CONSENT

Participating in Alzheimer s Disease Clinical Trials and Studies

The Clinical Trials Process an educated patient s guide

Power of Attorney for Health Care For

Classroom Activity: Research Jeopardy!

Phasel clinical trials:

What Happens Next? A PARENTS' A PARENTS GUIDE TO NEW YORK STATE CHILD PROTECTIVE SYSTEM

BIOPHARMACEUTICAL INDUSTRY IMPACT REPORT: Florida PRESENTED BY:

Information for patients and the public and patient information about DNA / Biobanking across Europe

Client Handbook. Workers Rehabilitation Services 21 Oak Street, 4 th Floor Hartford, CT (860)

Clinical Research Associate (CRA) - A Growing Career Path in Biotechnology / Pharmaceutical Industry

QUESTIONS YOU SHOULD ASK THE INSURANCE ADJUSTER

DEPUY HIP REPLACEMENTS: WHAT YOU NEED TO KNOW ABOUT THEM

Community Legal Information Association of PEI, Inc. Sexual Assault

A Practical Guide to. Hiring a LAWYER

The New Mental Health Act

APPENDIX B SAMPLE INFORMED CONSENT FORM

Probate and Estate Planning Section State Bar of Michigan. Acting for Adults who become Disabled

Selecting the Right Call Center Partner

Prescription Painkiller/Heroin Addiction and Treatment: The Patient Perception. Highlights

When should you call Best Doctors?

Checklist for Drafting LLC Operating Agreements. This is a summary checklist to review when drafting an LLC Operating Agreement.

Engaging E-Patients in Clinical Trials through Social Media. Patient Recruitment and the E-Patient: A Survey Analysis

Disclaimer. Objectives 5/30/2016

Tough Questions. Questions The Insurance Adjustors Don t Want You To Ask. By Christopher M. Davis, Attorney at Law

How to Complete This Power of Attorney for Healthcare

WHITE PAPER. CONVERTING SDTM DATA TO ADaM DATA AND CREATING SUBMISSION READY SAFETY TABLES AND LISTINGS. SUCCESSFUL TRIALS THROUGH PROVEN SOLUTIONS

Transcription:

understanding the informed consent process www.centerwatch.com

:: about this pamphlet Millions of volunteers participate in government-and industry-sponsored clinical trials each year. Prior to agreeing to participate, every volunteer has the right to know and understand what will happen during a clinical trial. This is called informed consent and it is a process that can help you decide whether or not participating in a trial is right for you. This pamphlet provides an overview of the informed consent process and helps you understand your rights and responsibilities as a study volunteer. Copyright 2001, 2003, 2009 by

:: your bill of rights If you have given consent to participate in a clinical trial, or if you have given consent on behalf of another person, you both are entitled to the following rights: To be told the purpose of the clinical trial To be told about all the risks, side effects, or discomforts that might be reasonably expected To be told of any benefits that can be reasonably expected To be told what will happen in the study and whether any procedures, drugs, or devices are different than those that are used in standard medical treatment To be told about all options available to you and how they are better or worse than being in a clinical trial To be allowed to ask any questions about the trial prior to consenting and/or at any time during the course of the trial To be allowed ample time, without pressure, to decide whether or not to consent to participate To refuse to participate, for any reason, before and after the trial has started To receive a signed and dated copy of the informed consent form To be told of any medical treatments available if complications occur during the trial

:: what you should know When you give written consent to participate in a clinical trial, you are acknowledging that you understand and accept all aspects of the study including any risks or benefits. However, informed consent is not strictly about signing a document. It is a process that involves ongoing conversations between the research staff and you before, and even after, you decide to become a study volunteer. To begin, the research staff is obligated to discuss all the pertinent information about the trial its purpose, the procedures involved, the potential risks and benefits with you. It is your responsibility to ask questions if there is something you do not understand. If you do not understand any part of the process, ask the researcher to repeat the information or to explain it in another way, using everyday words. If English is not your first language, inform the researcher that you are not comfortable speaking about a clinical trial in English. Upon request, research centers can and should produce documents that explain every aspect of the study and study personnel should be able to explain the information to you in your preferred language. If this is not possible, you should not participate in the study. It is the responsibility of the research staff to help you understand the information they provide you and to give you enough time to ask any additional questions you may have. In some instances, this may not be possible to accomplish in a single visit, therefore it is essential to take the time you need to make an informed decision. You may discover important concerns that you did not think about during the first visit.

:: what questions you should ask The following represents a sample list of questions that you should ask during the informed consent process: :: about the clinical trial What is the main purpose of the study? Why is this study important to me? What are the chances that this drug will work? What kinds of risks are involved? How much of my time will this take? Does the study involve a placebo or a treatment already on the market? :: about your care What kinds of tests will be done? Will they hurt? If so, for how long? How will the tests in the study compare to tests I would have outside the study? Will I be able to continue to see my own doctor during the study? Will I be able to continue to take my regular medications during the study? If I have side effects, can they be treated during the study? :: about personal matters Who will review information collected about me during the trial? What happens if I decide to quit the study? Can the investigator take me out of the study even if I want to continue? :: about compensation and costs Do I have to pay for any part of the study? If so, will insurance cover these costs?

:: take time to understand A recent survey of 590 study volunteers offers insight into the informed consent process and whether or not it is working to help volunteers understand their roles and responsibilities. Some key takeaways from the study are: Nearly 96% of volunteers said they received the informed consent form and 86% said they read the form completely. The vast majority of volunteers said they understood the expectations of the study, including additional risks and their ability to withdraw at any time. More than three-quarters understood that they could contact someone outside the study if they had additional questions about their rights during the trial. More than half the volunteers were unaware that neither their doctor nor they would know what medication they would receive during the study; more than two-thirds understood that they could receive a placebo in the trial. Nine out of 10 volunteers said that the information received prior to the trial matched their actual experience during the trial. Approximately 75% of the volunteers indicated that the main reason for participating in a study was to help themselves or others and to advance science. Research studies are very involved so it is important to learn as much as possible about the study you may participate in before you consent. The U.S. Food and Drug Administration (FDA) guidelines state that study volunteers should understand the risks they re taking, which may

Volunteer Understanding of Risk Percent of Study Volunteers 97% Agree 3% Disagree/ Unsure I understood that I could quit my study at any time. 91% Very Well/ Well 72% Agree 28% Disagree/ Unsure I understood that my study would carry additional risks and discomforts. Source: Survey of 672 Study Volunteers, 2009 mean spending additional time with the research staff to make sure you get the information you need. If you want to know details, such as any documented side effects of a particular drug observed in earlier clinical trials, you must ask for that information as well as any other information you may want to know. Volunteer Comprehension Percent of Study Volunteers 9% Not Well/ No Information The information received matched actual expererience. 82% Agree 18% Disagree/ Unsure I was made aware that I could contact someone other than the study doctor if I had questions regarding my rights. Source: Survey of 672 Study Volunteers, 2009 The decision to participate in a clinical trial is a personal one and one that you are entitled to make freely, without influence or coercion. Being properly informed so that you fully understand the responsibilities of becoming a study volunteer is the best way to ensure that you are making the right decision for you.

:: about Founded in 1994, is a trusted source and global destination for clinical trials information for both professionals and patients. A Boston-based publishing and information services company focusing on the clinical research industry, We provide proprietary data and information analysis on clinical trials through a variety of newsletters, books, databases, and information services used by pharmaceutical and biotechnology companies, contract research organizations (CROs), site management organizations (SMOs), and investigative sites involved in the management and conduct of clinical trials. As a pioneer in publishing clinical trials information, was the first Internet site to publish detailed information about active clinical trials that could be accessed by patients and their advocates. Today, we have one of the largest databases of clinical trials actively seeking patients on the Internet. For a comprehensive listing and detailed information about our publications and services, please visit our web site at www.centerwatch.com. S09609