№ files_lp_4_process_3_105264
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Character count: 4490
File size: 182 KB
Structured proposal form for submission to the DCF Institutional Review Board detailing research objectives, methodology, participant information, ethical considerations, and anticipated impact on DCF programs.
Note:
Year
Region/City:
Connecticut, USA
Topic:
Research and evaluation in social services
Document Type:
Research/Evaluation Proposal Form
Organization/Agency:
Department of Children and Families (DCF)
Author/Principal Investigator:
[Name not provided]
Intended Audience:
DCF IRB, researchers, academic institutions
Submission Date:
[Date not provided]
Project Duration:
[Start and end dates not provided]
Funding Source:
[Not specified]
Number of Subjects:
[Not specified]
Sites/Settings:
[Not specified]
Ethical Review:
Yes, IRB review required under 45 CFR § 46
Expected Impact:
Assessment of benefits and risks to subjects; evaluation of DCF project involvement
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2023
Region / City:
Wisconsin
Topic:
Child Care, Licensing Compliance
Document Type:
Form
Organization:
Department of Children and Families (DCF)
Author:
Wisconsin Department of Children and Families
Target Audience:
Child Care Centers
Period of Validity:
Ongoing
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2024
Region / City:
Milwaukee, Wisconsin
Theme:
Child protective services, Facility registration
Document Type:
Registration Form
Organization / Institution:
Division of Milwaukee Child Protective Services
Author:
Wisconsin Department of Children and Families
Target Audience:
Licensed facility providers
Period of validity:
January 1, 2024 - December 31, 2024
Approval Date:
November 1, 2024
Date of last changes:
N/A
Contextual Description:
Registration form for facilities seeking contracts with the Division of Milwaukee Child Protective Services to provide child welfare services.
Year:
Not specified
Region / City:
Not specified
Subject:
Youth development, case management, foster care
Document Type:
Policy, Procedures
Organization:
DCF (Department for Children and Families), YDP (Youth Development Program)
Author:
Not specified
Target Audience:
DCF and YDP staff, families, youth
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Amendments:
Not specified
Year:
FY 2023
Region / City:
USA
Topic:
Financial Analysis, Pharmaceutical Valuation
Document Type:
Investment Report
Organization / Institution:
N/A
Author:
N/A
Target Audience:
Investors, Financial Analysts
Period of Validity:
N/A
Approval Date:
N/A
Date of Changes:
N/A
Document type:
Consent form
Issuing body:
Department of Early Education and Care
Purpose:
Authorization of criminal and child welfare background record checks
Applicable programs:
Family Child Care License, Certified Assistant Certificate, Regular Assistant Letter of Approval
Required checks:
CORI, DCF records, SORI, fingerprint-based state and national criminal history
Validity period:
One year
Eligibility age:
15 years or older
Jurisdiction:
Massachusetts
Subject matter:
Background record check authorization
Administrative context:
Licensing and approval of family child care providers and assistants
Year:
2025
Region / City:
N/A
Field of Study:
Social Work
Document Type:
Program Plan
Institution:
N/A
Author:
N/A
Target Audience:
Students applying for the Spring 2025 cohort
Period of Action:
Spring 2025 to Spring 2027
Approval Date:
N/A
Revision Date:
N/A
Year:
2023
Region / City:
Wisconsin
Subject:
Workforce Development, Childcare Services
Document Type:
Report
Organization:
Wisconsin Department of Workforce Development
Author:
Division of Employment and Training
Target Audience:
Subaward recipients, project operators
Action Period:
Quarterly
Approval Date:
Not specified
Date of Amendments:
Not specified
Year:
2026
Region / State:
Kansas, USA
Subject:
Child welfare and foster care permanency
Document type:
Policy guideline
Agency / Institution:
Department for Children and Families (DCF)
Audience:
Prospective adoptive and permanent custodian families
Eligibility criteria:
Age, legal status, placement type, parental rights termination or consent
Assistance programs:
Adoption Assistance, Permanent Custodianship Subsidy (PCS)
Medical coverage:
Kansas Medical Card or equivalent state Medicaid
Financial support:
Monthly subsidy, special one-time payments for special needs
Legal documents:
Court orders for adoption or permanent custodianship
Assessment requirements:
Approved home assessment, training completion for adoptive parents
Year:
2026
Institution:
University of Kansas Medical Center (KUMC)
Document Type:
IRB Request Form / Research Protocol Submission
Target Audience:
Principal Investigators and Research Staff
Applicable Regulations:
45 CFR 46, 34 CFR 97, HHS Common Rule
Research Type:
Minimal Risk Behavioral and Biomedical Studies, Secondary Data Analysis
Submission Method:
myIRB Electronic Application
Required Materials:
Completed Form, Data Collection Sheets, Consent Forms, Recruitment Materials
Notes:
Includes guidance for flexible IRB review eligibility and types of research activities
Note:
Year
Subject:
IRB Member Performance Evaluation
Document Type:
Worksheet
Organization / Institution:
University of Miami
Target Audience:
IRB Chairs, IRB Managers
Period of Effectiveness:
Annual
Document type:
Institutional review form
Organization:
University of New England Institutional Review Board
Jurisdiction:
United States
Scope:
International human subjects research
Applicable research formats:
In-person research; Online-only research
Intended submitter:
Principal Investigator
Regulatory framework:
U.S. federal human subjects research regulations
Review body:
Institutional Review Board
Contact information:
[email protected]
Version date field:
Yes
IRB number field:
Yes
Target audience:
Faculty, staff, and student researchers
Geographic focus:
Research conducted outside the United States
Compliance topics:
Ethics approval, informed consent, data protection, export control regulations
Note:
Year
Document type:
Checklist
Target audience:
Investigators, IRB staff
Context description:
A checklist for investigators and IRB staff to assess and ensure regulatory compliance in clinical and non-clinical research studies.
Year:
2025
Region / City:
Louisiana
Topic:
Alcohol and Drug Survey
Document Type:
Guidelines
Organization / Institution:
Louisiana Board of Regents
Author:
Dr. Allison Smith
Target Audience:
IRB administrators, researchers, university staff
Period of Validity:
2025
Approval Date:
October 4, 2024
Amendment Date:
November 15, 2024
Year:
2023
Region / City:
Emory University
Topic:
IRB Determination for Research Involving Minors
Document Type:
IRB Determination Checklist
Organization:
Emory University
Author:
Emory Institutional Review Board (IRB)
Target Audience:
Researchers, IRB members, Clinical researchers, Academic institutions
Effective Period:
Ongoing
Approval Date:
2023
Date of Changes:
Not specified
Note:
Study Summary 1.1 Please provide a brief summary of the study in the table below. A complete description of the study with detailed information should be provided in the body of the protocol. For sections not applicable to the study, mark them as N/A. Study Title Study Design Primary Objective/Purpose Secondary Objective(s)/Purposes Research Intervention(s) ClinicalTrials.gov NCT # Study Population Sample Size Study Duration for individual subjects Study Specific Abbreviations/ Definitions
Background 3.1 Provide the scientific or scholarly background for, rationale for, and significance of the research based on the existing literature and how will it add to existing knowledge. :
this section should be limited to only information directly related to the research questions and objectives. Do not include your full dissertation proposal. 3.2 Describe any relevant preliminary data (e.g. pilot data).
Procedures Involved 5.1 Describe and explain the study design. 5.2 Please select the methods that will be employed in this study (select all that apply):
☐ Audio/Video Recording ☐ Psychophysiological Recording ☐ Behavioral Interventions ☐ Record Review - Educational ☐ Behavioral Observations and Experimentations ☐ Record Review - Employee ☐ Deception ☐ Record Review- Medical ☐ Focus Groups ☐ Record Review - Other ☐ Interviews ☐ Specimen Collection or Analysis ☐ Investigational Medical Device – (e.g. Medical Mobile Applications) ☐ Surveys and/or Questionnaires ☐Psychometric Testing ☐ Other Social-Behavioral Procedures Provide a description of all research procedures being performed and when they are performed. (Upload any surveys, questionnaires, interview scripts, focus group scripts, debriefing scripts, psychometric tests, stimulus materials, intervention manuals, and data collection forms on the Local Site Documents page in the IRB application.) 5.3 Describe the procedures or interventions that are going to be conducted as part of the research project, but that would have been conducted anyway, even if the research was not occurring (i.e. standard of care procedures, activities that would occur in a classroom). 5.4 Describe the procedures performed to lessen the probability or magnitude of risks of items selected in 5.2.5. 5 If accessing or collecting existing data, describe: The data that will be collected during the study (e.g. demographics, medical history, etc.). Attach the data capture sheet(s) on the Local Site Documents page in the IRB application. How the data will be obtained, including how you have the authority to access the data. The source or location of the data (e.g. USF Epic, TGH Epic, Hillsborough County School records, CANVAS records, publicly available databases, etc.). 5.6 If collecting and/or analyzing biological specimens, describe: How the biological specimens will be or have been collected. How the biological specimens will be stored. How long the biological specimens will be stored. How the biological specimens will be used. The laboratories that will be used. Whether the collected biological specimens will undergo genetic testing. If so, indicate if this study is part of a Genome Wide Association Study (GWAS) and whether the data will be forwarded to the NIH dbGaP. 5.7 If there are plans for long-term follow-up (once all research related procedures are complete), what data will be collected during this period.
Data and Specimen Storage for Future Research 6.1 If data or specimens will be banked for future research studies, describe where the data or specimens will be stored, how long it/they will b:
the process to request a release, approvals required for release, who can obtain data or specimens, and the data to be provided with specimens.
Note:
Year
Document Type:
Checklist
Author:
Dr. Twyla Williams-Damond
Context:
A checklist for ensuring all components are complete for an IRB application, including informed consent, recruitment templates, and readability reports.
Note:
Year
Document Type:
Checklist
Target Audience:
IRB members, researchers, committee staff
Context description:
A checklist for ensuring that IRB meeting minutes fulfill specific requirements related to protocol reviews and compliance with regulatory standards.