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Results Found: 97
  • Neurological Clinical Research Coordinators Perspectives on the Barriers and Strategies for Recruitment of Racial and Ethnic Minorities
    NYU Dataset

    Authors
    Sean J. Jaley
    Lauren Southwick
    Nina Parikh
    Jasmin Rivera
    2 more author(s)...
    Description

    This dataset was compiled through two semi-structured focus groups, conducted with a purposive sample of 29 clinical research coordinators (CRCs) at international stroke conferences in 2013 and 2014. The focus groups were conducted to gain an in-depth understanding of coordinator-level barriers to racial and ethnic minority recruitment and retention into neurological trials. Coded transcripts were created to define concepts, identify associations, summarize findings, and posit explanations. Participants discussed barriers related to translation, literacy, family composition, and severity of medical diagnosis as well as potential strategies to address these issues.

    Subject
    Delivery of Health Care
    Access Rights
    Application Required
    Author approval required
  • National Survey of Substance Abuse Treatment Services

    Alternate Title(s)
    N-SSATS
    Description

    The National Survey of Substance Abuse Treatment Services (N-SSATS) (formerly titled Uniform Facility Data Set (UFDS)) is designed to collect information from all facilities in the United States, both public and private, that provide substance abuse treatment. Data collected in N-SSATS include topics covering facility operation, services offered, primary focus, hotline operation, Opioid Treatment Programs and medications dispensed or prescribed, counseling and therapeutic approaches, special programs or groups, languages in which treatment is provided, type of treatment provided, number of clients, number of beds, types of payment accepted, sliding fee scale, and facility accreditation and licensure/certification.

    Subject
    Delivery of Health Care
    Geographic Coverage
    National
    Access Rights
    Free to All
  • New York City Clinical Data Research Network

    Alternate Title(s)
    NYC-CDRN
    Description

    The New York City Clinical Data Research Network (NYC-CDRN) is a project founded by the Patient Centered Outcomes Research Institute (PCORI) and is part of the PCORnet program. The NYC-CDRN longitudinal datasets bring together NYC organizations including medical schools, medical centers, research support organizations, and practice-based research networks. The NYC-CDRN datasets include longitudinally collected clinical, patient-reported, patient-generated. Datasets are available at the de-identified patient level, identifiable patient level, and patient cohort level.

    Subject
    Delivery of Health Care
    Geographic Coverage
    New York (City)
    Access Rights
    Application Required
    Local Expert for NYU
    Claudia Pulgarin
  • Daytime vs. Nighttime Admissions at an Academic Medical Center: NYU Langone Health EHR Dataset
    NYU Dataset

    Description

    This dataset was compiled to investigate the impact of daytime vs. nighttime admission on a general internal medicine service at an academic medical center, the following information was compiled: inpatient status, patient location, admission service, mortality rates, 30-day mortality rates, and variable cost for patients admitted between 6 PM-6 AM. This data was part of a project that retrospectively analyzed whether patients admitted overnight by a night float resident are associated with adverse patient outcomes such as inpatient and 30-day mortality as well as operational outcomes such as difference in length of stay, cost per case, and re-admission.

    Subject
    Delivery of Health Care
    Geographic Coverage
    New York (City)
    Access Rights
    Application Required
    NYU Langone Health Only
    Local Expert for NYU
    Harry Saag
  • Semi-structured interview and user testing data from the development and pilot testing of a behavioral economic-inspired electronic health record clinical decision support module
    NYU Dataset

    Authors
    Sara Kuppin Chokshi
    Hayley M. Belli
    Andrea B. Troxel
    Saul Blecker
    3 more author(s)...
    Description

    This dataset was collected as part of a test of a behavioral economic-inspired electronic health record (EHR) clinical decision support (CDS) module. In order to test the efficacy of behavioral economics “nudges” in the CDS module for promoting the Choosing Wisely Guidelines adherence for target hemoglobin A1c (HbA1c) levels, researchers performed:

    1. Key informant interviews (semi-structured interviews with individuals and small group experts in primary care, geriatrics, EHR, diabetes, and other fields);
    2. Group interviews (semi-structured interviews with groups of 4-6 clinicians);
    3. “Ride along” observation (individual observation session of clinician interaction with EHR real time, in situ);
    4. Think-aloud usability testing (Individual observations in “lab” of clinicians verbalizing all thoughts as they interact with the module following a carefully scripted series of EHR tasks);
    5. Near live (Individual observations in “lab” of clinicians interacting with simulated data and patient actors to realistically model clinical use of module);
    6. Live (Individual observations of clinicians in situ using the tool in actual patient care).

    Subject
    Delivery of Health Care
    Access Rights
    Application Required
    Author approval required
  • Physician Decision-Making During Active Surveillance of Prostate Cancer
    NYU Dataset

    Authors
    Stacy Loeb
    Caitlin E. Curnyn
    Angela Fagerlin
    R. Scott Braithwaite
    4 more author(s)...
    Description

    This dataset includes 24 structured, in-depth interviews with 24 physicians treating prostate cancer from diverse clinical backgrounds and geographic areas. These physicians were identified with purposive sampling strategies. An interview guide was developed based on a literature review and previous research on active surveillance, and interviews were conducted between July and December 2015. Each interview lasted between 22 and 51 minutes and was conducted either in-person or by telephone. Interviews focus on the use of active surveillance for prostate cancer and include questions on the use of specific protocols, how physicians choose the frequency of follow-up tests, opinions on testing options, and comfort levels with active surveillance.

    Subject
    Cancer
    Delivery of Health Care
    Geographic Coverage
    National
    Timeframe
    2015
    Access Rights
    Application Required
    Author approval required
  • Centers for Medicare and Medicaid Services

    Alternate Title(s)
    CMS
    Description

    Centers for Medicare and Medicaid Services (CMS) offers researchers and other health care professionals a broad range of quantitative information on programs, from estimates of future Medicare and Medicaid spending to enrollment, spending, and claims data, and a broad range of consumer research to help its partners and staff. CMS also conducts demonstration projects to explore alternative policies of health care coverage and delivery. National health expenditure data not specific to the Medicare or Medicaid programs are also included.

    Subject
    Delivery of Health Care
    Health Care Costs
    Geographic Coverage
    National
    Access Rights
    Free to All
    Fee Required
    Application Required
    Local Expert for NYU
    Caroline Blaum
    Danil Makarov
    Heather Gold
    James Slover
    Keith Goldfeld
    Saul Blecker
    Todor Mijanovich
  • Drug Abuse Warning Network

    Alternate Title(s)
    DAWN
    Description

    The Drug Abuse Warning Network (DAWN) is a nationally representative public health surveillance system that continuously monitors drug-related visits to hospital emergency departments (EDs). A DAWN case is any ED visit involving recent drug use that is implicated in the ED visit. The dataset includes demographics, up to 16 drugs involved in the ED visit, toxicology confirmation, route of administration, type of case, and disposition of the patient following the visit.

    Subject
    Delivery of Health Care
    Risk Factors
    Geographic Coverage
    National
    Access Rights
    Free to All
  • AMA Physician Masterfile

    Description

    The AMA Physician Masterfile includes education, training and professional certification information on virtually all Doctors of Medicine (MD) and Doctors of Osteopathic Medicine (DO) in the United States, Puerto Rico, Virgin Islands, and certain Pacific Islands. It includes current and historical data for more than 1.4 million physicians, residents, and medical students in the United States. This figure includes approximately 411,000 graduates of foreign medical schools who reside in the United States and who have met the educational and credentialing requirements necessary for recognition.

    Subject
    Delivery of Health Care
    Population Characteristics
    Geographic Coverage
    National
    Access Rights
    Fee Required
    Local Expert for NYU
    Heather Gold
  • TeleQuit MH Data
    NYU Dataset

    Alternate Title(s)
    TQMH
    Authors
    Scott Sherman
    Description

    The TeleQuit MH dataset provides research from a type-II hybrid effectiveness-implementation trial for the Veterans Health Administration. Data describes mental health clinic patients enrolled in a study aimed at developing a smoking cessation telephone care program, determining its effectiveness at long-term abstinence and comparing the VA telephone counseling to state-run quitlines. Approximately 1100 patients were referred.

    Subject
    Delivery of Health Care
    Risk Factors
    Geographic Coverage
    Multiple States
    Access Rights
    Author approval required