
Informed consent guidance and templates for psychologists
Jul 29, 2024 · For example, an informed consent form for a psychological assessment and evaluation practice will, and should, contain different information than an informed consent form for a …
Another example might be if the researcher determined that subjects were at risk for harming themselves or others. If the researcher felt bound to notify someone about that risk, subjects should …
Informed Consent Templates - Office of Research Ethics
Federal regulations outline informed consent requirements for non-exempt research, including a list of information participants must receive (i.e., elements of informed consent).
Informed Consent Guidelines & Templates – Human Research …
Apr 10, 2024 · IRB-HSBS has posted updated informed consent and assent templates. See the summary of changes for details. See the updated Basic Informed Consent Elements document for a …
IRB Consent Form Templates | Cornell Research Services
Jun 13, 2025 · A collection of informed consent, assent, and debriefing templates that can be used for your human participant research study.
Sample Consent Forms - UNC Research
Aug 5, 2024 · These consent form templates have been posted for your reference. When completing and IRB submission in IRBIS, please fill in the application and use the consent form builder specific …
Informed Consent in Research - Types, Templates and Examples
Mar 25, 2024 · This article explores the concept of informed consent, its types, the components of an informed consent form, and provides practical examples and templates to guide researchers.
Consent and Assent Form Templates - Human Research Protection …
There are separate consent templates for exempt research, which includes some research that involves educational tests, surveys, interviews or focus groups. This document will help you fill out the Plain …
Informed Consent Sample Forms - The Doctors
Our informed consent sample forms address common patient safety and risk scenarios. Customize them to your practice and your patients to enhance the informed consent process.
The researcher signature section below is not required, but is recommended for research studies involving an in-person consent procedure, especially when consent may be obtained by multiple …