Trial site population diversity check

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Each tool's price and track record across every agent today. Empty means the call worked and found nothing.

# Trial site population diversity check

For one trial (or a planned site list) and one condition. Diversity plans are judged against who has the disease, so both sides must be cited.

## 1. The sites

1. Open the trial with @[ClinicalTrials.gov · Study](alexandria:clinicaltrials-gov/clinical-trials/study) (nct_id): enrolment target, eligibility, and every site with city and state.
2. If planning a new trial, list comparable studies with @[ClinicalTrials.gov · Search](alexandria:clinicaltrials-gov/clinical-trials/search) (condition, status completed) and read their sites the same way.

## 2. Who lives near each site

3. Resolve each site's county with @[US Census Bureau · Geographies](alexandria:census-gov/census/geographies).
4. Pull race and ethnicity, age 65 and over, and limited-English households with @[US Census Bureau · Data](alexandria:census-gov/census/data) (acs/acs5, county).

## 3. Who has the disease

5. Search @[PubMed · Search](alexandria:pubmed-ncbi-nlm-nih-gov/publications/search) (condition plus prevalence or incidence by race and ethnicity, United States) and read the best sources with @[PubMed · Article](alexandria:pubmed-ncbi-nlm-nih-gov/publications/article). Keep group-specific rates only where stated.
6. Check how past trials in the condition reported enrolment with @[Research Index · Search papers](alexandria:firecrawl-research-index/search) (condition plus trial diversity or underrepresentation).

## Write the scorecard

- **Site table:** site, county, share by group, 65+, limited English.
- **Gap:** groups with high disease burden that few sites serve.
- **Suggestions:** regions or site types to add, and language support needs.
- **Sources:** NCT ids, ACS tables, PMIDs and paper ids. Say what could not be found.

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