№ files_lp_4_process_3_068152
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The document is a comprehensive health survey questionnaire used for annual collection of data on health status, healthcare access, and related conditions in the United States.
Year:
2024
Region / City:
United States
Topic:
Health Status, Health Care Access, Exercise, Chronic Health Conditions
Document Type:
Survey Questionnaire
Organization:
Centers for Disease Control and Prevention (CDC)
Author:
CDC
Target Audience:
General Public, Health Researchers
Effective Period:
2024
Approval Date:
Not specified
Modification Date:
Not specified
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
1986–2017
Region:
Massachusetts, USA
Subject:
Public health data collection and surveillance
Document type:
Report appendix
Organizations:
Massachusetts Department of Public Health (MDPH), Centers for Disease Control and Prevention (CDC)
Target population:
Adults, youth, and specific populations including LGBTQ, immigrants, veterans, and people with disabilities
Survey types:
BRFSS, YRBSS, YHS
Language:
English
Data characteristics:
Self-reported, cross-sectional
Limitations:
Incomplete population coverage, restricted survey administration, gaps in real-time and standardized data, lack of detailed demographic or community-specific data
Sexual orientation and gender identity inclusion:
Since 1993 for youth and 2000 for adults, with expanded questions in 2007 and 2013
Year:
2015
Region / City:
National
Subject:
Behavioral Risk Factor Surveillance System
Document Type:
Report
Organization / Institution:
Population Health Surveillance Branch (PHSB)
Author:
Not specified
Target Audience:
States, health professionals, data analysts
Effective Period:
Ongoing (up to 2017 and beyond)
Approval Date:
2015
Date of Amendments:
2016
Year:
2020
Region / City:
United States
Topic:
Behavioral Risk Factors, Public Health Survey
Document Type:
Report
Organization / Institution:
Centers for Disease Control and Prevention (CDC)
Author:
Not specified
Target Audience:
Public health professionals, policymakers, state health departments
Period of Effectiveness:
Not specified
Approval Date:
June 10, 2020
Modification Date:
Not specified
Year:
2021
Region / city:
United States
Topic:
Behavioral Risk Factor Surveillance System (BRFSS)
Document type:
Protocol
Organization:
Centers for Disease Control and Prevention (CDC)
Author:
Centers for Disease Control and Prevention (CDC)
Target audience:
Data collectors, health department personnel, public health officials
Period of validity:
2021 and ongoing
Approval date:
2021
Date of changes:
N/A
Year:
2019
Region / city:
United States, Guam, Puerto Rico
Topic:
Health Risk Factors, Chronic Diseases, Preventive Health Services
Document Type:
Technical Documentation
Agency / Organization:
Centers for Disease Control and Prevention (CDC)
Author:
CDC, State Health Departments
Target Audience:
Public Health Officials, Researchers, Policy Makers
Effective Period:
2019
Approval Date:
2019
Modification Date:
None listed
Document Type:
Change Request
Program:
Behavioral Risk Factor Surveillance System (BRFSS)
Subject:
Revisions to 2024 BRFSS Questionnaire and Data Collectors’ Protocol
OMB Number:
0920-1061
OMB Expiration Date:
March 31, 2025
Date:
November 14, 2023
Issuing Organization:
Centers for Disease Control and Prevention (CDC)
Geographic Scope:
50 U.S. states, Washington DC, and U.S. territories
Data Collection Methods:
Landline interviews, cell phone interviews, in-person interviews
Core Sections (2024):
15
Optional Modules (2024):
26
Related Attachments:
Attachment 5a – 2024 BRFSS Questionnaire; Attachment 10a – 2024 Calling Protocol and Dispositions
Purpose:
OMB approval of revisions for the 2024 BRFSS survey instrument and calling protocol
Population:
Adult respondents in participating states and territories
Authors:
Valeriya Vasenina, MS; Divya Sood, MD; Adam Hanley, PhD; Julie Fritz, PhD; Erin P. Ward, MD
Affiliations:
University of Utah; Oregon Health and Science University; University of Florida
Corresponding author:
Erin P. Ward, MD
Email:
[email protected]
Data source:
2022 Behavioral Risk Factor Surveillance System (BRFSS)
Conducting body:
Centers for Disease Control and Prevention (CDC)
Year of data:
2022
Geographic scope:
United States
Study population:
U.S. adults aged 18 years and older with a history of cancer
Sample size:
72,765 cancer survivors
Study design:
Cross-sectional population-based survey analysis
Primary focus:
Association between history of depression and quality of life among cancer survivors
Key variables:
Mental health days, physical health days, emotional support, social isolation, cancer-related pain, functional limitations
Statistical methods:
Chi-square analysis; Stata SE v19.5
Disclosures:
No financial disclosures
Year:
2013
Survey:
Ci3 2013 BRFSS
Subject:
Disposition coding for telephone survey outcomes
Document Type:
Instructional guidance
Related Standards:
American Association of Public Opinion Research (AAPOR)
Codes Referenced:
5400, 4400, 5150, 3150, 5300, 4300, 5220, 2220, 5140, 3140
Scope:
Technological Barriers, Telecommunication Barriers, Phone Circuit Messages, Answering Devices
Intended Audience:
Interviewers and data collectors
Context:
Transition to four-digit disposition codes
Source Context:
2013 BRFSS conference discussions
Year:
2021
Region / City:
United States
Theme:
Health Survey
Document Type:
Questionnaire
Organization / Institution:
Centers for Disease Control and Prevention (CDC)
Author:
CDC/ATSDR
Target Audience:
US residents
Period of validity:
2021
Approval Date:
3/31/2021
Revision Date:
N/A
Year:
2009
Region / City:
Queensland
Topic:
Criminal History Disclosure, Guide, Hearing, and Assistance Dogs
Document Type:
Legal Guide
Organization / Institution:
Guide, Hearing and Assistance Dogs Team
Author:
Not specified
Target Audience:
People applying for approval as guide, hearing, or assistance dog trainers or employee trainers
Period of Validity:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2026
Organization:
Texas Department of Insurance
Document Type:
Amendment Proposal Form
Related Manual:
2026 Valuation Manual, VM-20
Sections:
9.F.3, 9.F.4, Appendix 2
Author:
Rachel Hemphill
Date Received:
10/28/25
Notes:
2025-15 VM-20, Section 9.F.3 and 9.F.4
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.
Language:
English
Document type:
Manuscript template
Intended use:
Scholarly article preparation
Structure elements:
Abstract, sections, subsections, figures, tables, references
Affiliation format:
Department, Institution, City, Country
Author information:
Author names and e-mail placeholder
Citation style:
Numbered references
Figure and table captions:
Included as placeholders
Content status:
Placeholder and sample text
Year:
2022
Organizations:
Peninsula Clean Energy (PCE), Silicon Valley Clean Energy (SVCE), East Bay Community Energy (EBCE)
Document Type:
Code Amendment Recommendations
Scope:
Residential and Nonresidential EV Charging Requirements
Version Dates:
May 11, 2022; July 8, 2022; September 2022; October 2022
Target Audience:
Local jurisdictions and code administrators
Reference:
2022 Title 24 Part 11 California Green Building Standards Code (CALGreen)
Topics:
EV Charging Stations, EV Ready Spaces, Direct Current Fast Charging, Automatic Load Management Systems, Multifamily and Nonresidential Buildings
URL:
BayAreaReachCodes.Org
Year:
2026
Region / city:
UK
Subject:
Electric Vehicle Charge Points, Heat Pumps, and connection procedures
Document Type:
Application form
Organization / institution:
Distribution Network Operators (DNOs)
Author:
Not specified
Target audience:
Individuals or entities installing electric vehicle charge points (EVCP) or heat pumps (HP)
Effective Period:
Ongoing
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2025
Region / City:
California
Subject:
Vehicle Emission Standards
Document Type:
Regulatory Proposal
Agency:
California Air Resources Board
Author:
California Air Resources Board
Target Audience:
Manufacturers, Automotive Industry
Effective Period:
2025–2028
Approval Date:
N/A
Revision Date:
N/A
Note:
Year
Topic:
Academic Promotion and Tenure
Document Type:
Instructional Guidelines
Organization / Institution:
Auburn University
Target Audience:
Faculty, Department Chairs, University Administrators
Context:
Instructional guidelines for faculty members preparing their dossiers for promotion and tenure evaluations.
Year:
N/A
Region / City:
California
Document Type:
Legal Text
Organ / Institution:
California Department of Industrial Relations
Author:
N/A
Validity Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A