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
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
Underutilization of patch testing for contact dermatitis: insights from DataDerm. (JAAD)
The 2024 annual report of DataDerm: the database of the American Academy of Dermatology.(JAAD)
Patient characteristics, diagnostic testing utilization, and antifungal prescribing pattern for onychomycosis in the USA: a cohort study using DataDerm, 2016-2022.(Skin Appendage Disord.)
Contact us
If you have questions, please contact the DataDerm team at datadermanalytics@aad.org.
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