ArticleJournal of biomedical informatics2015
Standardizing data exchange for clinical research protocols and case report forms: An assessment of the suitability of the Clinical Data Interchange Standards Consortium (CDISC) Operational Data Model (ODM).
Article in Journal of biomedical informatics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
30 citing papers in PubMed.
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- A SARS-CoV-2 minimum data standard to support national serology reporting.Annals of clinical biochemistry · 2024Article
- The Journey to a FAIR CORE DATA SET for Diabetes Research in Germany.Scientific data · 2024Article
- Clinical Research Informatics: a Decade-in-Review.Yearbook of medical informatics · 2024Review
- Next-generation study databases require FAIR, EHR-integrated, and scalable Electronic Data Capture for medical documentation and decision support.NPJ digital medicine · 2024Article
- Rethinking clinical study data: why we should respect analysis results as data.Scientific data · 2022Article
- A Semi-Automated Term Harmonization Pipeline Applied to Pulmonary Arterial Hypertension Clinical Trials.Methods of information in medicine · 2022Article
- Securely sharing DSMB reports to speed decision making from multiple, concurrent, independent studies of similar treatments in COVID-19.Journal of clinical and translational science · 2022Article
- From biobank and data silos into a data commons: convergence to support translational medicine.Journal of translational medicine · 2021Article
- Pragmatic MDR: a metadata repository with bottom-up standardization of medical metadata through reuse.BMC medical informatics and decision making · 2021Article
- Evaluating the Coverage of the HL7AMIA ... Annual Symposium proceedings. AMIA Symposium · 2020Article
- Proposed minimum information guideline for kidney disease-research and clinical data reporting: a cross-sectional study.BMJ open · 2019Article
- Data Lakes, Clouds, and Commons: A Review of Platforms for Analyzing and Sharing Genomic Data.Trends in genetics : TIG · 2019Review
- Integrative LHS for precision medicine research: A shared NIH and Taiwan CIMS experience.Learning health systems · 2019Article
- Improving the Patient-Clinician Interface of Clinical Trials through Health Informatics Technologies.Journal of medical systems · 2018Review
- ODM Data Analysis-A tool for the automatic validation, monitoring and generation of generic descriptive statistics of patient data.PloS one · 2018Article
- Towards achieving semantic interoperability of clinical study data with FHIR.Journal of biomedical semantics · 2017Article
- Advances in Clinical Decision Support: Highlights of Practice and the Literature 2015-2016.Yearbook of medical informatics · 2017Review
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
Efficient communication of a clinical study protocol and case report forms during all stages of a human clinical study is important for many stakeholders. An electronic and structured study representation format that can be used throughout the whole study life-span can improve such communication and potentially lower total study costs. The most relevant standard for representing clinical study data, applicable to unregulated as well as regulated studies, is the Operational Data Model (ODM) in development since 1999 by the Clinical Data Interchange Standards Consortium (CDISC). ODM's initial objective was exchange of case report forms data but it is increasingly utilized in other contexts. An ODM extension called Study Design Model, introduced in 2011, provides additional protocol representation elements. Using a case study approach, we evaluated ODM's ability to capture all necessary protocol elements during a complete clinical study lifecycle in the Intramural Research Program of the National Institutes of Health. ODM offers the advantage of a single format for institutions that deal with hundreds or thousands of concurrent clinical studies and maintain a data warehouse for these studies. For each study stage, we present a list of gaps in the ODM standard and identify necessary vendor or institutional extensions that can compensate for such gaps. The current version of ODM (1.3.2) has only partial support for study protocol and study registration data mainly because it is outside the original development goal. ODM provides comprehensive support for representation of case report forms (in both the design stage and with patient level data). Inclusion of requirements of observational, non-regulated or investigator-initiated studies (outside Food and Drug Administration (FDA) regulation) can further improve future revisions of the standard.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.