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DataDerm data request program


DataDerm® is the AAD’s clinical data registry, comprising real-world, longitudinal clinical data from more than 16 million unique patients and over 70 million encounters, representing the largest database of dermatologic data in the world. The DataDerm Data Request Program is designed to make DataDerm’s data available to AAD members in a de-identified, aggregate format to support scholarly research and quality improvement projects. The database is best suited to support retrospective, observational, descriptive studies that evaluate population-level patterns or trends over time.

Through the program, data request proposals will be reviewed and selected on an annual basis. For selected data request projects, the research team will work closely with DataDerm analytics staff to analyze the hypothesis and prepare figures and tables for subsequent publication or presentation.

Program timeline

  • March 27, 2026: Window to submit data request proposals opens.

  • May 1, 2026: Window to submit data request proposals closes.

  • June 2026: Proposals selected.

  • July-December 2026: Collaboration with DataDerm analytics staff.

  • December 2026: Analytics work complete.

  • March 2027: Manuscript or publication complete, project closes.

DataDerm request proposals

Proposals will be accepted for submission starting March 27, 2026.

  • Database overview
  • Eligibility & requirements
  • Recent publications
  • Database overview

    DataDerm is a retrospective, patient-level repository of Electronic Health Record (EHR) data collected from participating practices nationwide. Data are securely extracted from practice EHR systems and aggregated into a centralized research database. Although the data support Merit-based Incentive Payment System (MIPS) reporting, the database extends well beyond quality reporting and is designed to facilitate clinically meaningful research.

    Data available for research include, but are not limited to:

    • Patient information such as date of birth, gender, geographic location, or insurance

    • Visit information such as place of service, clinician type, or visit type

    • Clinical and medical information such as diagnoses, medications, procedures, or comorbidities

    Data not currently available for research include: laboratory results (including external labs), claims, cost and billing data, scheduling data, patient correspondence records, external pathology reports, and images.

    Data linkage opportunities

    When appropriate and available, the database can be linked with external datasets to enhance research projects. Previous linkages have included:

    • National Plan and Provider Enumeration System (NPPES)

    • Rural-Urban Commuting Area (RUCA) data

    • U.S. Census data

    • Private institutional datasets

    Linkages may be conducted at the:

    • Patient level

    • Clinician level

    • Practice or location level

    These linkages can support studies examining access to care, geographic variation, workforce trends, and social determinants of health.

    Eligibility

    To submit a proposal, you must have current AAD membership, up-to-date disclosures, and adherence to authorship and conflict-of-interest rules. Submissions are limited to one per individual per year. You must have an AAD member sponsor if you are a student, international fellow, affiliate, or adjunct. To ensure fairness, the program does not accept proposals from members of the Data Governance Task Force (DGTF) or DataDerm Oversight Committee (DDOC).

    Proposal selection process and criteria

    The DGTF uses a structured and transparent process to evaluate proposals requesting access to DataDerm. Each proposal is assessed for its relevance to current unmet needs in dermatology, feasibility for the DataDerm database, clarity of the research approach, and potential to advance patient care, education, and future research. Final selection decisions are based on scores and DGTF discussion, with constructive feedback shared with applicants whenever possible.

    To align with assessment criteria, your proposal should be a concise document no more than 3 pages (single-spaced, 11 point Arial font, 0.5 inch margins) that emphasizes both scientific rigor and strategic alignment with the AAD mission. Proposals must be written to highlight the significance of the work to clinical dermatology and AAD membership.

    Required proposal sections

    Significance: Explain the project’s relevance to dermatology and to the AAD membership.

    • How it fits into current dermatology knowledge

    • How it addresses AAD priorities

    • Impact of the award on the field of dermatology

    • Impact of the award on the career trajectory of the investigator

    Innovation: Identify the specific gaps in existing literature this study fills, such as:

    • How this expands existing knowledge that can’t be done with other study types

    • Methodological or technical innovation that will result in new analysis frameworks or quality benchmarks

    • Why other existing databases are insufficient to answer the question

    Approach and analytic plan: This section should include:

    • Specific aim(s)

    • A clear testable hypothesis

    • Planned methods for testing the hypothesis

    • An expected treatment effect and power analysis

    • Potential pitfalls and alternative analysis plans

    • A table of key variables needed from the DataDerm registry

    • Expected results and future work

    References: This section does not count toward the 3 page limit


    Contact us

    If you have questions, please contact the DataDerm team at datadermanalytics@aad.org.

    Additional resources


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