Instructions for Developing an Informed Consent Document General Information. Describe the purpose(s) of this research study in lay terms. Purpose of the Study. Procedures. Risks. Benefits. Compensation, Costs and Reimbursement. Withdrawal or Termination from Study. Confidentiality.
Please indicate with your signature on the space below that you understand your rights and agree to participate in the experiment. Your participation is solicited, yet strictly voluntary. All information will be kept confidential and your name will not be associated with any research findings.
4.3. What are the requirements for obtaining a valid consent? Four core criteria must be met: the patient giving consent must have capacity • the consent must be freely given • the consent must be sufficiently specific to the procedure or treatment proposed • the consent must be informed.
Follow these steps to write an effective consent form. Step 1: Title and introduction. Step 2: Description of the activity. Step 3: Risks and benefits. Step 4: Confidentiality and data handling. Step 5: Voluntary participation and withdrawal. Step 6: Consent statement. Step 7: Signature and date. Step 8: Contact information.
You should focus on explaining why the question is important, summarizing the history of the question, and describing previous theories and data that are relevant to the study you will describe. Finally, you should present the hypothesis that you have tested (or will test) in your study.
Basic Elements of Informed Consent Purpose of the Research. Description of the Research. Risks. Benefits. Alternatives to Participation.
Instructions for Developing an Informed Consent Document General Information. Describe the purpose(s) of this research study in lay terms. Purpose of the Study. Procedures. Risks. Benefits. Compensation, Costs and Reimbursement. Withdrawal or Termination from Study. Confidentiality.
Instructions for Developing an Informed Consent Document General Information. Describe the purpose(s) of this research study in lay terms. Purpose of the Study. Procedures. Risks. Benefits. Compensation, Costs and Reimbursement. Withdrawal or Termination from Study. Confidentiality.
If you prefer to write your own consent document, you may do so, but be sure to include all required elements of informed consent.