Biomedical Signal Extraction From Symptom Descriptions: An Observational Registry Using the OpenGenome Platform
OGNOME-REG
Accuracy and Calibration of Evidence-Grounded Biomedical Signal Extraction From Free-Text Symptom Descriptions: A Prospective Observational Registry Using the OpenGenome Automated Research Instrument
1 other identifier
observational
1,000
1 country
1
Brief Summary
This registry prospectively collects anonymized free-text symptom descriptions submitted voluntarily by adults through the OpenGenome platform at opengenome.bio. For each submission, the system retrieves real biomedical literature from PubMed and ClinicalTrials.gov in parallel, applies a constrained reasoning model operating under a strict output schema, and returns a structured biological signal report. The study evaluates the internal consistency of extracted signals, the calibration of confidence scores relative to dataset size and symptom specificity, and the distribution of biological signal categories across a large anonymous population. No intervention is assigned. No participant contact occurs. All data is anonymized at the point of collection.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2026
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 5, 2026
CompletedStudy Start
First participant enrolled
May 5, 2026
CompletedFirst Posted
Study publicly available on registry
May 11, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 5, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 30, 2028
May 19, 2026
May 1, 2026
2 years
May 5, 2026
May 16, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Internal signal-source concordance rate
Proportion of primary signal claims in generated reports that are traceable to at least one retrieved PubMed or ClinicalTrials.gov source included in the same report
At point of automated report generation, assessed continuously over 12 months
Study Arms (1)
Voluntary Submitters
Adults aged 18 or older who voluntarily submit a free-text symptom description via the OpenGenome platform and receive a structured biological signal report. No intervention is assigned.
Interventions
AI-assisted biomedical signal extraction from free-text symptom descriptions, cross-referenced against PubMed and ClinicalTrials.gov evidence sources.
Eligibility Criteria
Adults aged 18 years or older who voluntarily access the OpenGenome platform at opengenome.bio and submit a free-text description of symptoms or health-related observations for automated biomedical signal analysis.
Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.
Sponsors & Collaborators
- OpenGenomelead
Study Sites (1)
OpenGenome
Friedrichshain, State of Berlin, 10243, Germany
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- ECOLOGIC OR COMMUNITY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- NETWORK
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 5, 2026
First Posted
May 11, 2026
Study Start
May 5, 2026
Primary Completion (Estimated)
May 5, 2028
Study Completion (Estimated)
May 30, 2028
Last Updated
May 19, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share
Individual participant data is not available as all submissions are fully anonymous with no participant identifiers collected. Aggregate deidentified summary statistics will be made available upon study completion.