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Results Found: 10
  • The State Ambulatory Surgery and Services Databases

    Alternate Title(s)
    SASD
    Description

    The State Ambulatory Surgery and Services Databases (SASD) are State-specific files that include data for ambulatory surgery and other outpatient services from hospital-owned facilities. In addition, some States provide ambulatory surgery and outpatient services from nonhospital-owned facilities. The uniform format of the SASD helps facilitate cross-State comparisons. The SASD are well suited for research that requires complete enumeration of hospital-based ambulatory surgeries within geographic areas or States.

    Subject
    Medicine & Health
    Geographic Coverage
    United States
    Access Rights
    Fee required
  • National Emergency Medical Services Information System

    Alternate Title(s)
    NEMSIS
    Description

    The National Emergency Medical Services Information System (NEMSIS) is the national database that is used to store EMS data from the U.S. States and Territories. NEMSIS is a universal standard for how patient care information resulting from an emergency 911 call for assistance is collected. NEMSIS is a collaborative system to improve patient care through the standardization, aggregation, and utilization of point of care EMS data at a local, state and national level. NEMSIS is a product of NHTSA’s Office of EMS and in collaboration with the University of Utah is the host of the Technical Assistance Center.

    Subject
    Medicine & Health
    Geographic Coverage
    United States
    Access Rights
    Application required
    Free to all
  • Evaluation of Victim Advocacy Services for Battered Women in Detroit, 1998-1999
    WSU Dataset

    Authors
    Arlene Weisz
    Description

    This study evaluated advocacy services offered to battered women in Detroit, Michigan, and examined other aspects of coordinated community responses to domestic violence by focusing on women named as victims in police reports. Advocacy was defined as those services provided to support victims during the legal process or to enhance their safety. For the Preliminary Complaint Reports Data (Part 1), a random sample of preliminary complaint reports (PCRs), completed by police officers after they responded to domestic violence calls, were gathered, resulting in a sample of 1,057 incidents and victims. For Victim Advocacy Contact Data (Part 2), researchers obtained data from advocates' files about the services they provided to the 1,057 victims. For Case Disposition Data (Part 3), researchers conducted a computer search to determine the outcomes of the cases. They looked up each perpetrator from the list of 1,057 incidents, and determined whether there was a warrant for the focal incident, whether it turned into a prosecution, and the outcome. The Initial Victim Interview (Part 4) and Follow-Up Victim Interview Data (Part 5) were conducted from April 1998 to July 1999. During the same period that researchers were completing the second interviews, they also interviewed 23 women (Victim Comparison Group Interview Data, Part 6) from the list of 1,057 whom they had been unable to reach during the first interviews. They compared these 23 women to the 63 who had second interviews to determine if there were any differences in use of services, or views toward or participation in prosecution. Variables in Part 1 focus on whether alcohol and abuse were involved, previous incidents, the suspect's psychological aggressions and physical assaults, if a weapon was used, if the victim was hurt, if property was damaged, if the victim sought medical attention, and the severity of physical abuse or injury. Variables in Part 2 provide information on the role of the advocate, methods of contact, types of referrals made, and services provided. Variables in Part 3 include the type of charge, outcome of resolved case, why the case was dismissed, if applicable, and if the suspect was sentenced to probation, costs, confinement, no contact with the victim, a batterer program, or community service. [...]

    Subject
    Sociology
    Geographic Coverage
    Detroit, Michigan
    Timeframe
    1998 - 1999
    Access Rights
    Application required
  • MDHHS MiTracking - Michigan Environmental Public Health Tracking

    Description

    From the MDHHS website: "The MiTracking Program gathers existing Michigan-specific environmental and health data and provides them in one online location. These data can be easily queried on the MiTracking data portal. Results are provided in tables, charts, and maps that can be downloaded, saved, and printed. The data provided by the MiTracking program can create greater awareness of environmental health concerns, and inform public health actions and programs."

    Subject
    Medicine & Health
    Statistics
  • Wayne State University - National Science Foundation Data Management Plan Evaluation
    WSU Dataset

    Authors
    James Van Loon
    Katherine G. Akers
    Cole Hudson
    Alexandra Sarkozy
    Description

    To determine the overall quality of Data Management Plans (DMPs) at Wayne State University, the Library System’s Research Data Services (RDS) team evaluated the content of 119 DMPs from grant proposals submitted to the National Science Foundation by Wayne State University researchers between 2012 and 2014. The DMPs were evaluated using a 15-question modified rubric previously used by researchers at University of Michigan.

    Subject
    Computer Science
    Timeframe
    2012 - 2014
    Access Rights
    Free to all
  • The National Survey on Drug Use and Health

    Alternate Title(s)
    NSDUH
    Description

    The National Survey on Drug Use and Health provides up-to-date information on tobacco, alcohol, and drug use, mental health and other health-related issues in the United States. NSDUH began in 1971 and is conducted every year in all 50 states and the District of Columbia. Information from NSDUH is used to support prevention and treatment programs, monitor substance use trends, estimate the need for treatment and inform public health policy.

    Subject
    Medicine & Health
    Geographic Coverage
    United States
    Access Rights
    Free to all
  • Behavioral Risk Factor Surveillance System

    Alternate Title(s)
    BRFSS
    Description

    The Behavioral Risk Factor Surveillance System (BRFSS) is a system of health-related telephone surveys that collect state data about U.S. residents regarding their health-related risk behaviors, chronic health conditions, and use of preventive services. BRFSS collects data in all 50 states as well as the District of Columbia and three U.S. territories. BRFSS collects state data about U.S. residents regarding their health-related risk behaviors and events, chronic health conditions, and use of preventive services. BRFSS also collects data on important emerging health issues such as vaccine shortage and influenza-like illness. Interviewers administer the annual BRFSS surveys continuously through the year.

    Subject
    Medicine & Health
    Geographic Coverage
    United States
    Timeframe
    1984 - Present
    Access Rights
    Free to all
  • Systems Change Analysis of Sexual Assault Nurse Examiner Programs in One Midwestern County of the United States, 1994-2007
    WSU Dataset

    Alternate Title(s)
    SANE
    Authors
    Rebecca Campbell
    Deborah Bybee
    J. Kevin Ford
    Debra Patterson
    Description

    The purpose of this study was to determine whether adult sexual assault cases in a Midwestern community were more likely to be investigated and prosecuted after the implementation of a Sexual Assault Nurse Examiner (SANE) program, and to identify the 'critical ingredients' that contributed to that increase. The data are divided into six parts: Part 1, Study 1: Case Records Quantitative Data; Part 2, Study 2: Case Characteristics Quantitative Data; Part 3, Study 3: Police and Prosecutors Interview Qualitative Data; Part 4, Study 4: Police Reports Quantitative Data; Part 5, Study 5: Survivor Interview Qualitative Data; Part 6, Study 6: Forensic Nurse Interview Qualitative Data.

    Subject
    Law
    Timeframe
    1994 - 2008
    Access Rights
    Application required
    Free to all
  • National Evaluation of the Robert Wood Johnson Foundation's Urban Health Initiative: Survey of Adults and Youth

    Alternate Title(s)
    Evaluation of the Urban Health Initiative: Working to Ensure the Health and Safety of Children
    Authors
    Beth C. Weitzman
    Description

    This dataset was generated during a repeated cross-sectional national telephone survey of households, conducted as part of the evaluation of the Robert Wood Johnson Foundation's Urban Health Initiative (UHI). UHI is a long-term effort to improve the health, safety, and well-being of children and youth in five economically distressed cities in the United States: Baltimore, MD, Detroit, MI, Oakland, CA, Philadelphia, PA, and Richmond, VA. The UHI Survey of Adults and Youth (SAY) included a variety of questions, asked of both parents and their 10-18 year old children, regarding children's health, safety, perceptions of neighborhoods and schools, family relations, quality of city services, and other issues. SAY surveyed 3 types of households -- households without children, households with children aged 0-9 years, and households with children aged 10-18 years -- in up to 14 geographic areas, including the 5 UHI program cities, 9 comparison cities demographically similar to the UHI cities, the suburban regions of these cities, the most populous 100 United States cities, and the rest of the country. There were 3 waves of SAY fielded during the course of the UHI project: during the 1998-1999, 2001-2002, and 2004-2005 school years. There is a separate data file for each wave, and each record contains all of the data for a given household.

    Subject
    Medicine & Health
    Sociology
    Geographic Coverage
    United States
    Timeframe
    1998 - 2005
    Access Rights
    Application required
    Fee required
  • National Vulnerability Database

    Alternate Title(s)
    NVD
    Description

    The National Vulnerability Database (NVD) is the U.S. government repository of standards based vulnerability management data represented using the Security Content Automation Protocol (SCAP). This data enables automation of vulnerability management, security measurement, and compliance. The NVD includes databases of security checklist references, security related software flaws, misconfigurations, product names, and impact metrics. Originally created in 2000 (called Internet - Categorization of Attacks Toolkit or ICAT), the NVD has undergone multiple iterations and improvements and will continue to do so to deliver its services. The NVD is a product of the NIST Computer Security Division, Information Technology Laboratory and is sponsored by the Department of Homeland Security’s National Cyber Security Division. The NVD performs analysis on CVEs that have been published to the CVE Dictionary. NVD staff are tasked with analysis of CVEs by aggregating data points from the description, references supplied and any supplemental data that can be found publicly at the time. This analysis results in association impact metrics (Common Vulnerability Scoring System - CVSS), vulnerability types (Common Weakness Enumeration - CWE), and applicability statements (Common Platform Enumeration - CPE), as well as other pertinent metadata. The NVD does not actively perform vulnerability testing, relying on vendors, third party security researchers and vulnerability coordinators to provide information that is then used to assign these attributes.

    Subject
    Computer Science
    Timeframe
    2000 - Present
    Access Rights
    Free to all

 

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