
THIS YEAR'S FAIR DATES ARE March 31 - April 2, 2009!
SCIENTIFIC REVIEW COMMITTEE INFO CAN BE FOUND HERE
Doing the paperwork for a Science Fair project can take as long as the project itself, and is frequently a source of frustration. The Ozarks Science and Engineering Fair did not create these forms; however, they must be used if we are to be affiliated with the International Science and Engineering Fair (ISEF). We hope that the following information will assist teachers and students in filling out the forms in less time and with fewer frustrating mistakes.
The first section below will help you determine which forms you will need for any particular project, and will help with Forms 1A and 1B (which everyone needs). Included in these instructions is information about what type of projects will need approval BEFORE they can be started, and who must approve them. Other sections will then provide assistance with filling out the other forms, and include a list of common mistakes that you will want to avoid.
![]()
Forms 1A and 1B are REQUIRED on EVERY project, and what you put on Form 1A determines what other forms are also required. First, fully complete the top of Form 1A, parts 1-7. Note that there is a separate Form 1A for TEAM projects. Specific things to watch for include:
The Adult Sponsor (part 3), usually the student's teacher
You must indicate the PROJECTED start and end dates (the dates you plan to start and end your laboratory/field research) in part 5.
ACTUAL start date MUST BE after all necessary signatures and approvals have been obtained.
![]()
Microorganisms that are cultured from ANY environment are considered potentially pathogenic. Standard microbiological handling practices MUST be used when working with cultured organisms. If your project involves the growth of microorganisms (this includes but is not limited to viruses, viroids, prions, bacteria, fungi, and parasites), you must check the pathogenic agent box on Question 3 on the "Checklist for Adult Sponsor/Safety Assessment" (Form 1), Question 8 on the "Research Plan" (Form 1A), and Question 5 on the "Qualified Scientist" (Form 5), and file the appropriate forms for Pathogenic Agents.
ONLY Escherichia coli (E.coli) strain K12 and Baker's/Brewers Yeast (saccharomyces cerevisiae) are not considered to be pathogens. All other strains of E. coli are considered to be pathogenic.
Forms REQUIRED for Pathogenic Agents:
Checklist for Adult Sponsor/Safety Assessment Form 1
Research Plan 1A
Approval Form 1B - NOTE: Pathogenic Agents require SRC approval BEFORE experimentation begins.
Qualified Scientist Form 2
Forms that MAY be required:
Designated Supervisor Form 3 - NOTE: If the Qualified Scientist cannot be present during experimentation, you MUST file a Designated Supervisor form. This person will supervise your project in the absence of the Qualified Scientist.
Registered Research Institution/Industrial Setting Form 1C - NOTE: If work was conducted or equipment used at an institutional or industrial setting at any time during the current ISEF project year, you must complete this form after the completion of the experiment.
![]()
TOP 10 MISTAKES
Click on any of the links in the table below for hints on avoiding the most
common errors and omissions.
The Pathogenic Agent box must be checked on the following forms: Checklist for Adult Sponsor/Safety Assessment Form 1 question 3, Research Plan 1A question 8, and Qualified Scientist Form 2 question 5.
Required forms are missing.
Pathogenic Agents require SRC approve BEFORE experimentation begins.
On Research Plan Form 1A question 6, DO NOT CHECK THE HOME BOX. You can collect your samples at home, you can streak plates or inoculate broth at home, but you CANNOT incubate or work with microbial cultures in your home. This must be done in a laboratory either at school or in a research institution.
The Qualified Scientist must have an earned doctorate degree in an appropriate discipline that would qualify them to oversee the experiment. Alternatively, the Qualified Scientist must have a master's degree and sufficient work experience in an area that is related to the specific project.
Form 1A Research Plan question 9, part C - the procedure descriptions are sometimes very vague and do not make sense. The Research Plan should be a detailed description of your research method or procedure. After you have written out your procedure, go over this with your qualified scientist or supervisor to verify that you have written out the procedure correctly and in sufficient detail.
Return to Top 10 Mistakes/Return to Top of Page
![]()
Avoiding human research out of fear of complications and/or paperwork: Many studies can be done based on simple observations of legal public behavior, normal classroom activities, or publicly available data. These require no consent forms or qualified scientist forms. As examples, students can get data from newspapers such as learning the average age of criminal offenders; from classrooms, such as who sits on the front row of classes, males or females?; or by observing driving or shopping behaviors that occur in public.
Not including a psychologist or psychiatrist on the IRB when the study concerns behavior: If your school needs help with this issue, please contact the Missouri State Psychology Department, or Dr. Matthew Fanetti [Federal Law (25-CFR-46)].
Not assessing risk adequately: Risk is explained on page 12 of the International Rules. While risk is clearly explained here, students have proposed to study exercise, very personal feelings, and even special medical conditions in invasive ways, without a qualified scientist. The IRB needs to review the risk discussion.
The IRB not meeting as a group: The IRB does need to meet as a group to discuss the proposal. Too often, students have walked their proposals around for signatures, and careful consideration of the proposals did not occur. That is how one student secured permission to require medical patients to forego use of their prescribed medical equipment.
The IRB Chair not providing a signature on the Approval Form (1B): It is in small print, but the IRB Chair must sign the 1B Form.
Not providing Informed Consent Form (4B) for subjects under 18 years of age: This is required even if the study involves no risk, except under certain conditions mentioned on page 11 of the International Rules.
Not checking the appropriate box for human research on the Research Plan (1A), under Section 8: A simple omission that often causes problems.
Omitting the start and end dates for the study on the Research Plan (1A): See item 5, please.
Omitting the bibliography required as per Research Plan (1A): See item 9d, please.
Return to Top 10 Mistakes/Return to Top of Page
![]()
All Nonhuman Vertebrate Animal projects require:
Abstract
Checklist for Adult Sponsor
Research Plan Form 1A
Approval Form 1B
Qualified Scientist Form 2
Nonhuman Vertebrate Animal Project Form 5
Nonhuman Vertebrate Animal projects may also require the following:
Registered Research Institutional/Industrial Setting Form 1C
Designated Supervisor Form 3
this form is required if the Qualified Scientist listed on Form 2 does not directly supervise the student/project.
For Nonhuman Vertebrate Animal projects, FOUR references are required with one of the references being an animal care reference (see Form 1A line 9d).
The start date of the project must be AFTER SRC approval (see Form 1A line 5).
The animal care supervisor listed on the bottom of Form 5 must be the person who directly supervises the care and handling of the vertebrate.
Alternatives to the use of Nonhuman Vertebrate Animal projects for research must be explored and discussed in the Research Plan (Form 1A line 9c).
Research Plan (Form 1A line 9c) must include a statement that a weight loss or growth retardation of 15% in any group of animals in the project will cause an immediate termination of the project.
Nonhuman Vertebrate Animal projects require an extremely detailed Research Plan (Form 1A line 9c). Please see page 16, second column, of the International Rules.
The specific amount and dose of any compounds given to the animals in the project must be listed in detail in the Research Plan (Form 1A line 9c).
All of the forms must be FULLY COMPLETED.
Return to Top 10 Mistakes/Return to Top of Page
![]()
CHEMICALS AND DEVICES
Use this information if you use any chemicals and/or devices.
Do you use one or more of the following? (Your first job is to know the definition of each.)
Controlled Substances (see the International Rules to see form list)
Hazardous Substances (see the International Rules to see form list)
Hazardous Devices (see the International Rules to see form list)
In some cases, it is the substance itself which is controlled or hazardous. In other cases, whether a substance is controlled or hazardous is determined by the concentration and/or combination of substances. In most cases, the student should discuss these terms with his or her teacher.
If you do have one or more of the above in your proposed research project, plan to fill out the required forms and locate the necessary people to supervise you.
Qualified Scientist - Form 2 (see the International Rules)
Designated Supervisor - Form 3 (see the International Rules)
Adult Sponsor - Form 1 (see the International Rules)
You must plan for proper storage and disposal of your chemical substances when the project is finished.
Return to Top 10 Mistakes/Return to Top of Page
![]()
This page has been visited
times.
![]()
This page maintained by Sue McCrory
Missouri State University
Last updated
Wednesday, July 09, 2008