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Middle Tennessee Science & Engineering Fair 2014. Training & Information Workshop Sponsored by. MTSEF and ISEF. Middle TN Science & Engineering Fair (MTSEF)- an ISEF affiliated fair Thursday, March 20 - Saturday, March 22, 2014 http://www.apsu.edu/mtsef
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Middle Tennessee Science & Engineering Fair2014 Training & Information Workshop Sponsored by
MTSEF and ISEF • Middle TN Science & Engineering Fair (MTSEF)- an ISEF affiliated fair Thursday, March 20 - Saturday, March 22, 2014 http://www.apsu.edu/mtsef • International Science & Engineering Fair (ISEF) LA Convention Center, Los Angeles, CA May 11-16, 2014 http://www.sciserv.org/isef • MTSEF follows rules and guidelines established by the ISEF. • Questions: schillers@apsu.edu (SRC); woodsn@apsu.edu (IRB); mtsef@apsu.edu (MTSEF) • Questions: SRC@sciserv.org -- ISEF
Scientific Review Committee (SRC) • SRC examines projects for the following: • evidence of literature search • evidence of proper supervision • use of accepted research techniques • completed forms, signatures & dates • evidence of search for alternatives to animal use • humane treatment of animals • compliance with rules & laws governing human & animal research • appropriate use of recombinant DNA, pathogenic organisms, controlled substances, tissues & hazardous substances & devices • appropriate documents & substantial expansion for continuation projects.
SRC Process • Before Experimentation: • SRC reviews projects involving: • Vertebrate Animals • Potentially hazardous biological agents • Microorganisms • recombinant DNA • Tissues • SRC also reviews & forwards to IRB projects involving humans.
SRC Process • After Experimentation: SRC reviews and approves previously approved & all other projects to ensure Research Plan & Rules were followed.
The Paper Trail • All SRC & IRB forms are submitted to SRC through Dr. Steve Hamilton (APSU, PO Box 4718, Clarksville TN 37044; hamiltonsw@apsu.edu) • SRC reviews forms, forwards projects involving Human subjects to IRB. • Researcher notified of SRC & IRB decisions. • Communication by email & by U.S. mail • Revisions submitted by researcher. • Researcher notified of SRC & IRB decisions.
Required SRC Forms: All Projects • For All Projects • Checklist for Adult Sponsor (1) • Research Plan • Student Checklist (1A) • Approval Form (1B) • Regulated Research Institutional/Industrial Setting Form (1C) - if applicable • Continuation Form (7) – if applicable
Required SRC Forms • Some Projects Require Additional Forms Human Subjects Vertebrate Animals Potentially Hazardous Biological Agents Hazardous Chemicals, Activities & Devices
Required Forms:Human Subjects • For Projects Involving Human Subjects, add: • Human Subjects Form (4) • Qualified Scientist Form (2) if applicable • Must have IRB approval prior to experimentation
Required Forms: Vertebrate AnimalsNon-Regulated Site • Vertebrate Animal Form (5A) • 5A is for Research in a Non-Regulated Site (Eg. Home, school, farm, ranch, in the field) if the following applies: research involves behavioral, observational or supplemental nutritional studies on animals & Non-invasive/ non-intrusive methods that do not negatively affect an animal’s health or well-being. • Must have SRC approval prior to experimentation
Required Forms: Vertebrate AnimalsRegulated Research Institution • Vertebrate Animal Form (5B), • Qualified Scientist Form (2) • Must have IACUC approval prior to experimentation
Required Forms:Potentially Hazardous Biological Agents • Potentially Hazardous Biological Agents Risk Assessment Form (6A) • Human & Vertebrate Animal Tissue form (6B) • Qualified Scientist Form (2) if applicable • Risk Assessment Form (3) • Must have SRC approval prior to experimentation.
Required Forms:Hazardous Chemicals, Activities and Devices • Risk Assessment Form (3) • Qualified Scientist Form (2)
Adults Involved Forms for All Human Subjects Vertebrate Animals Potentially Hazardous Biological Agents Hazardous Chemicals Devices Activities More Detail Definitions & Forms
Adult sponsor • Oversees project to make sure that student • is informed of ISEF Rules and Guidelines • is aware of risks associated with project • is aware of forms required for project • will receive proper supervision during experimentation • if required, submits project to IRB or SRC • Teacher usually serves as Adult Sponsor
Qualified Scientist • Required for some projects • Doctoral/professional degree related to student research or Masters degree with SRC approval • Completes Form 2 – QS Form
Designated Supervisor • Animal Care Supervisor for vertebrate animal projects • Supervises projects involving hazardous chemicals, activities or devices • Supervises projects requiring a Qualified Scientist when the Qualified Scientist cannot directly supervise the student
IRB (Institutional Review Board) • Reviews human participants studies • Membership must include: • an educator • a school administrator • someone knowledgeable about evaluating physical and/or psychological risk: MD, PA, RN, psychologist, licensed social worker or licensed clinical professional counselor
SRC (Scientific Review Committee) • Reviews some projects before experimentation • Reviews all projects just prior to competition • Membership must include: • a biomedical scientist (Ph.D., M.D., D.V.M., D.D.S., PharmD., D.O.) • an educator • one other member
A Research Plan is required for all projects. It must incorporate all of the relevant topics listed in the Research Plan Instructions.
Studies conducted at a research institution, industrial setting or any work site other than home, school or field require Form 1C
Continuation studies • Project based on prior research in the same field of study • Longitudinal studies are permitted • Multi-year study • Studies time-based change • Require form 7
What are human participants studies? Human participants studies involve living individuals where there is • Intervention or interaction with participants and/or • Collection of identifiable private information
Exempt studies – do not require IRB review nor human participants forms • Product testing of a student invention, program, concept, etc. • No health hazards • No personal data collected • Feedback directly related to product • Studies using pre-existing, publicly available human data
Additional exempt studies • Behavioral observations in unrestricted public settings • No interaction • No manipulation of environment • No recording of any personal identifiers • Studies using certified de-identified/ anonymous data
Human participants research • The IRB must review and approve the research plan before experimentation begins • Research participants 18 years of age or older must give informed consent • Research participants under 18 must give assent and their parents may be required to give permission
Human participants research, cont’d • The IRB evaluates the project and determines • Risk level • Requirement for Qualified Scientist • Requirement for written informed consent/assent/parental permission
Risk evaluation • No more than minimal risk Anticipated harm and discomfort not greater than encountered in daily life • More than minimal risk Anticipated harm or discomfort is greater than encountered in daily life • More than minimal risk studies should require written consent/assent and parental permission. Final determination for this requirement made by the IRB
Types of Risk • Physical risks • Exercise • Ingestion, tasting, smelling, application of substances • Exposure to potentially hazardous material • Psychological risks • Invasion of privacy • Participant is a member of an at-risk group
If IRB determines that written informed consent/assent or parental permission is required, documentation is obtained on an “informed consent” document
What is a vertebrate animal? • Live, nonhuman vertebrate mammalian embryos or fetuses • Bird and reptile eggs within 3 days of hatching • All other nonhuman vertebrates (including fish) at hatching or birth • Zebrafish embryos 7 days (168 hours) post fertilization
Prohibited studies • Induced toxicity studies involving known toxic substances that could impair health or destroy life • Behavioral experiments with • Conditioning using aversive stimuli • Mother/infant separation • Induced/learned helplessness • Studies of pain • Predator/vertebrate prey experiments
No vertebrate animal deaths due to the experimental procedures are permitted • Studies designed or anticipated to cause vertebrate animal death are prohibited. • Any deaths must be investigated by a qualified individual • If death was the result of experimental procedure the study must be terminated and the study will not qualify for competition.
Behavioral observations of animals are exempt from SRC review if • There is no interaction with the animals and • There is no manipulation of the environment and • All federal or state fish, game and wildlife regulations are followed
School/Home/Field Regulated Research Institution (musthave an IACUC review and approval process) Universities Government research agencies Private research laboratories Research sites
Requirements for studies at school/home/field • Agricultural, behavioral, observational or supplemental nutritional studies and • Non-invasive and non-intrusive with no negative effect on animal’s health or well-being and • Require SRC pre-review and approval
Additional requirements for studies at school/home/field • SRC determines level of supervision appropriate for the study: • Designated supervisor • Veterinarian • Qualified scientist • Form 5A required