RESEARCH SUBJECT INFORMATION SHEET FOR ADOLESCENTS:
RESEARCH SUBJECT INFORMATION SHEET FOR
NON-CLINICAL STUDIES WITH CHILDREN (Ages 7 – 14)
|GENERAL INSTRUCTIONS FOR USING THIS FORM: |
|This template includes shaded boxes providing brief instructions. Other instructions are shaded or underlined and in parentheses. Delete all shaded|
|and underlined instructional text in parentheses BEFORE submitting this form to the SLU IRB for review. To delete an instruction box, place your |
|curser within the shaded box, right click the mouse, and select “Delete Rows”. To delete shaded or underlined text, select the text by |
|highlighting with your mouse, and push the “delete” button on your keyboard. |
| |
|Customize the text in this information sheet to fit your study. |
|Print this form on University letterhead. |
| |
|Instructions for the consent form header below: |
|List all sites (under SLU IRB jurisdiction) in which the research study will take place below SAINT LOUIS UNIVERSITY. |
|Insert the IRB # obtained from eIRB. |
|The “Title of Project” should match the protocol title. This title should also match the sponsor contract or grant title if appropriate. |
SAINT LOUIS UNIVERSITY
|Participant: | |IRB #: | |
| |First Name / Last Name | |
|Principal Investigator (PI) | |Contact | |
| | |Phone # | |
| |First Name / Last Name Credentials | |
|Title of Project: | |
You are being asked to participate in a research study because you (state the reason).
The researcher wants to learn more about (insert age-appropriate description of research topic).
In this research study you will (list study procedures).
This study will last (list participant duration).
If the study activities make you feel bad or hurt, you must tell your parents or the researcher.
You don’t have to be in this research study if you don’t want to.
If later you have any questions about this study, please ask your parents/guardian or call the researcher, (insert researcher name), at (insert phone number).
|SAINT LOUIS UNIVERSITY – INSTITUTIONAL REVIEW BOARD – APPROVAL STAMP |
| |
|This form is valid only if the IRB’s approval stamp is shown below. |
| |
................
................
In order to avoid copyright disputes, this page is only a partial summary.
To fulfill the demand for quickly locating and searching documents.
It is intelligent file search solution for home and business.
Related download
- template clinical study protocol
- rmp template 2 0 1 draft
- project summary for non clinical studies
- nci dctd crada model 03 10 2017 v1 0 revised 10 31 17
- investigator brochure authoring instructions
- research subject information sheet for adolescents
- clinical interventional study protocol template
- glp compliance
Related searches
- cdc flu information sheet 2019
- basic contact information sheet printable
- new patient information sheet template
- counselors for adolescents near me
- mmr vaccine information sheet cdc
- fact information sheet florida
- mmr vaccine information sheet spanish
- product information sheet sample
- information sheet template
- product information sheet template
- information sheet template word
- client information sheet template