The following charts show the forms that are required for the different types of research projects. The forms with a white background are REQUIRED for that particular project type. The forms with a gray background MAY BE REQUIRED, please refer to the ISEF Rulebook for specifics. If you click on the form name, you can download the needed forms using Adobe Acrobat Reader.
- Requirements for ALL Research Projects
- Additional Requirements for Human Subjects Research Projects
- Additional Requirements for Vertebrate Animal Research Projects
- Additional Requirements for Potentially Hazardous Biological Agent Research Projects
- Additional Requirements for Projects Using Hazardous Chemicals, Devices & Activies
- Projects that are being continued from previous years need to have a completed Continuation Projects Form (7)
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Tips for Forms & Projects: Abstracts: CSEF Finalists MUST use the CSEF Abstract form and NOT the ISEF Official Abstract Form. Abstracts should be written in past tense and should include the objective(s) of the study, the general procedure(s) used, the result(s) of the study and the significance of the result(s). The abstract should not include acknowledgements (such as referencing mentors or laboratories involved in the project). Read more information on writing abstracts. Checklist (1): The Checklist for Adult Sponsors form is to be used by the Adult Sponsor when reviewing students' research plans and seeing that the proper approvals are acquired BEFORE research on the project begins. This means it should be signed and dated BEFORE research begins - attesting to the fact that the Adult Sponsor has indeed done his/her job in guiding the student researcher in getting the proper approvals. Student Checklist (1A): When completing #6 (Start Date), please remember that we are looking for the date that the student began his/her laboratory and/or data collection work - not when the background research began. The actual start date and the projected start date can be the same, or the actual start date can be months from the projected start date, just so long as all approvals have been acquired BEFORE the ACTUAL research start date. Also, on #7, remember that field work is data collection that is done away from the school, home and/or research institute (i.e.: collection of data at different stream sites around the state, collection of surveys at sites such as businesses and/or schools other than the student researcher's, observations done in public places, etc.). If there is field work done, we need a list of all of those sites and addresses if possible (general locations if not). Research Plan: This information MUST be TYPED. When writing the research plan, please have students clearly identify each of the four points needed in the plan: Question Being Addressed; Hypothesis/Problem/Engineering Goal(s); Procedures/Methods; and Bibliography. This will aid in the review of the research plans and cut down on the need for clarification in many cases. Please see Page 31 of the ISEF Rulebook for more details on what should be addressed if using human subjects, vertebrate animals, potentially hazardous biological agents and/or hazardous chemicals, activities & devices. Approval Form (1B): All approval signatures for #1 and #2 (if applicable) MUST be acquired BEFORE a student can begin his/her laboratory/data collection work. Please note that the Adult Sponsor no longer signs this form. He/She is required to sign the Adult Sponsor Checklist for approval. Registered Research Institutional/Industrial Setting Form (1C): This is the only form that is required to be completed AFTER experimentation has been completed. Please pay particular attention to the signature box- if the student did the research at the institution, then that institution must have given their approval if it involves human subjects, vertebrate animals or potentially hazardous biological agents. For example, Colorado State University has its own Regulatory Compliance Board and if a student were to go there to do a research project with a professor (or anyone else), the student's research must be approved by this board and the CSU board overrides any decision a school IRB may have made regarding the study, as the school has no jurisdiction at CSU. |
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SAMPLE FORM 4's See the answers to a sample Form 4 where the IRB has determined there is Minimal Risk and Informed Consent is RECOMMENDED, but Not Required. See the answers to a sample Form 4 where the IRB has determined there is Minimal Risk and Informed Consent is REQUIRED. See the answers a sample Form 4 where the IRB has determined there is More than Minimal Risk and Informed Consent and a Qualified Scientist are REQUIRED. |
Tips for Forms & Projects: There is no such thing as NO RISKS. If no risks are anticipated, then use the phrase "NO KNOWN RISKS." If there are different procedures that different groups of subjects will be taking place in, the you will need SEPARATE Form 4's for each procedure and each procedure will need to be approved by the IRB. Please note that the Adult Sponsor's name and contact information MUST be included on Form 4 for consent reasons. Subjects and their parents need to be able to get in touch with someone in charge of the study if need be. Also note that this form can be used as a form to gain consent for using pictures of the subjects. If the IRB feels that the procedures are not appropriate, then they will not sign the form and the student will have to change his/her study to meet any changes they recommend. Please make sure that the Medical Professional's specialty is circled. If they don't fit into any of those categories, then they should not be reviewing projects as a Medical Professional. Please note that school nurses are now allowed to be the Medical Professional on the IRB. In rural areas of the state where a medical professional is hard to come by, please contact CSEF SRC for assistance. Neither the Adult Sponsor, parent(s), Qualified Scientist, nor the Designated Supervisor who oversees a specific project is permitted to serve on the IRB reviewing that project. This eliminates any conflict of interest. IRB approval is needed BEFORE laboratory/data collection begins. Read more about ISEF rules regarding Human Subject research. IRB's may use this power point presentation as a training guide on how to review student research projects.
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SAMPLE FORM 5A's See a sample Form 5A where the SRC has determined a Designated Supervisor is REQUIRED. See a sample Form 5A where the SRC has determined a Veterinarian and Designated Supervisor are REQUIRED. See a sample Form 5A where the SRC has determined a Veterinarian, a Designated Supervisor and Qualified Scientist are REQUIRED. SAMPLE COMPLETED FORM 5B's See a sample completed Form 5B. |
Tips for Forms & Projects: Vertebrate Animal research includes projects involving:
Vertebrate Animal research projects are categorized into two categories, those that can be done at a non-regulated site and those that must be done at a regulated research institution. Vertebrate Animal studies may be conducted at a non-regulated research site (home, school, farm, ranch, in the field, etc.) ONLY if each of the following applies:
All other studies using vertebrate animals must be conducted at a regulated research institution. If there are unexpected deaths in either the experimental or control groups, the cause of the death must be investigated. If the experimental procedure is responsible for the deaths, the experiment must be immediately terminated. A death rate of 30% or greater in any group or subgroup is not permitted and the project will fail to qualify for competition. Research Projects at Non-Regulated Sites The SRC must decide what type of supervision the project requires:
Form 5A must be filled out by the researcher for each different type of animal being used and includes the number of animals being used in the study, the housing and husbandry to be provided, and what will happen to the animals after experimentation. Research Projects at Regulated Research Institutes Form 5B must be filled out by the Qualified Scientist or the Principle Investigator at the regulated research institution. A copy of the regulated research institution IACUC approval letter must be attached to this form. The Qualified Scientist must describe the USDA Pain Category that the research falls under. The local SRC must also review the project to certify that the research complies with ISEF rules. This review should happen before experimentation begins. Proper euthanasia at the end of experimentation for tissue removal and/or pathological analysis is permitted. Only the Qualified Scientist or an institutional representative may perform the euthanasia. The following types of studies on vertebrate animals are prohibited:
SRC approval is needed BEFORE laboratory/data collection begins. Read more about ISEF rules regarding Vertebrate Animal research. |
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SAMPLE FORM 6A's See a sample Form 6A where the SRC has determined the risk level of the study is BSL-1. See a sample Form 6A where the SRC has determined the risk level of the study is BSL-2. See a sample Form 6A where the research was done at a regulated research institution. SAMPLE COMPLETED FORM 6B's See a sample Form 6B. |
Tips for Forms & Projects: Projects incorporating microorganisms (including bacteria, viruses, viroids, prions, rickettsia, fungi, and parasites), recombinant DNA (rDNA) technologies or human or animal fresh tissues, blood or body fluids may involve working with potentially hazardous biological agents. When dealing with potentially hazardous biological agents, it is the responsibility of the student and all of the adults involved in a research project to conduct a risk assessment. Risk assessment defines the potential level of harm, injury or disease to plants, animals or humans that may occur when working with biological agents. Experimentation with potentially hazardous biological agents is prohibited in a home environment. Research with unknown microorganisms can be treated as a BSL-1 study under the following conditions:
If a culture is opened for identification, sub-culturing or isolation, it must be treated as a BSL-2 study and involve BSL-2 laboratory procedures. The following types of tissue do not need to be treated as potentially hazardous biological agents:
SRC approval is needed BEFORE laboratory/data collection begins. Read more about ISEF rules regarding Potentially Hazardous Biological Agents projects. |
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SAMPLE FORM 3's See a sample Form 3 where the student was using Hazardous Chemicals. See a sample Form 3 where the student was using Hazardous Activities. See a sample Form 3 where the student was using Hazardous Devices. |
Tips for Forms & Projects: It is important that the Designated Supervisor include ALL hazardous chemicals, activities and/or devices that will be used in the project under #1 and answer the remaining questions for each one. If firearms and/or bows and arrows are used, it is important that you include a copy of the student's and supervisor's Colorado Hunter Safety Card. Just as a scientist needs to be qualified in the area of research that a student is working in, a Designated Supervisor may need to explain their qualifications. For example, if a student were using power tools, it would be appropriate to have someone who is a carpenter by trade supervising the student, even though the parent or teacher may know how to use the tools. Being MOM or DAD is not necessarily qualification enough to supervise a project using hazardous chemicals or devices. Read more about ISEF rules regarding using Hazardous Chemicals, Devices and Activies in research. |
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Last modified 10/2/08