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Human Subjects Approval Request
I. General Information
Title of Study
*
Project starting date
*
Month
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1924
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1922
1921
1920
Project ending date
Month
1
2
3
4
5
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7
8
9
10
11
12
Day
1
2
3
4
5
6
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11
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15
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28
29
30
31
Year
2025
2024
2023
2022
2021
2020
2019
2018
2017
2016
2015
2014
2013
2012
2011
2010
2009
2008
2007
2006
2005
2004
2003
2002
2001
2000
1999
1998
1997
1996
1995
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1992
1991
1990
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1984
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1971
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1968
1967
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1965
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1962
1961
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1956
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1953
1952
1951
1950
1949
1948
1947
1946
1945
1944
1943
1942
1941
1940
1939
1938
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1935
1934
1933
1932
1931
1930
1929
1928
1927
1926
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1924
1923
1922
1921
1920
Principal Investigator
*
Mailing Address
*
Street Address
City
Alabama
Alaska
American Samoa
Arizona
Arkansas
California
Colorado
Connecticut
Delaware
District of Columbia
Florida
Georgia
Guam
Hawaii
Idaho
Illinois
Indiana
Iowa
Kansas
Kentucky
Louisiana
Maine
Maryland
Massachusetts
Michigan
Minnesota
Mississippi
Missouri
Montana
Nebraska
Nevada
New Hampshire
New Jersey
New Mexico
New York
North Carolina
North Dakota
Northern Mariana Islands
Ohio
Oklahoma
Oregon
Pennsylvania
Puerto Rico
Rhode Island
South Carolina
South Dakota
Tennessee
Texas
Utah
U.S. Virgin Islands
Vermont
Virginia
Washington
West Virginia
Wisconsin
Wyoming
Armed Forces Americas
Armed Forces Europe
Armed Forces Pacific
State
ZIP Code
Phone
*
Email
*
Co-Investigator(s)
Funding Source
Faculty/Advisor/Sponsor
Department or School
(if Applicable)
Review Type Requested
*
- Select -
Exempt
Expedited Review
Full Review
Revised Submission
For more information, see
item 5
in this One Stop Solution. If this request is a Revised Submission, please include original request form.
II. Research Description
Statement of the research problem
*
Number, type of participants/sample
1
and special characteristics.
2
Number
Type of Participant/Sample
Special Characteristics
Actions
Edit
Delete
There are no
Entries.
Add Entry
Maximum number of entries reached.
Will participants receive any type of compensation for their participation?
*
- Select -
Yes
No
Describe the compensation
Do the participants belong to any of the following protected populations?
Check all that apply.
Minors (17 or younger)
Individuals who are cognitively impaired or unable to give consent
Prisoners
Pregnant women and fetuses
Any individual who might not be capable of making an informed decision concerning participation e.g.., persons with mental illness or psychiatric disability, economically disadvantaged, educationally disadvantaged.
Using participants from any of the above categories requires submission of HSAR II.
Will deception be involved?
*
If “Yes” submit HSAR II.
- Select -
Yes
No
Does the study involve any sensitive topics that might adversely affect the participant’s reputation, character, or employment (e.g., sexual or illegal behaviors)?
*
If “Yes” submit HSAR II
- Select -
Yes
No
Sequential Outline of Procedures
*
III. Data Collection
Instruments:
List and attach all tests, questionnaires, interview protocols, observation schedules, etc. and list the type of subjects to whom each will be applied (See II. B. for types and characteristics):
Instrument
Type of Subject(s)
Actions
Edit
Delete
There are no
Entries.
Add Entry
Maximum number of entries reached.
Methods of collecting the data
*
Is confidentiality insured
*
- Select -
Yes
No
If “Yes” please specify how you will handle confidential data during and after your study: If “No” explain:
Confidentiality Explanation
*
Attach copies of any instruments used and informed consent statements or forms.
Drop files here or
Select files
Max. file size: 12 MB.
1
Type: student, teacher, faculty, administrator, etc.
2
Special Characteristics: achievement levels, socioeconomic status, exceptionalities, neighborhoods, etc.
Phone
This field is for validation purposes and should be left unchanged.