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patient-consent-simplifier

Simplifies informed consent documents into patient-friendly language while maintaining regulatory compliance. Readability assessment targeting 6th-8th grade level, risk/benefit clarification in table format, and FDA 21CFR50/ICH-GCP/HIPAA compliance validation.

52

Quality

60%

Does it follow best practices?

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Adds up to 20 points to the overall score

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SecuritybySnyk

Passed

No findings from the security scan

Fix and improve this skill with Tessl

tessl review fix ./scientific-skills/Other/patient-consent-simplifier/SKILL.md
SKILL.md
Quality
Evals
Security

Quality

Content

56%Weight 40%Scale 1-5

Reviews the quality of instructions and guidance provided to agents. Good implementation is clear, handles edge cases, and produces reliable results.

The skill has a well-structured workflow with checkpoints and feedback loops, but its code examples are largely non-executable against the provided bundle and reference a fictitious API/module. Reconciling the documented API with scripts/main.py would most improve actionability and progressive disclosure.

Suggestions

Align all code examples with the actual bundle: import from scripts.main and use only the methods that exist (simplify(text), calculate_grade_level(text)), or extend main.py to implement simplify_section, clarify_risks, assess_readability, and check_compliance.

Fix the referenced file path: the CLI examples invoke scripts/consent_simplifier.py but the bundled file is scripts/main.py.

Split the detailed capability API, the compliance checklist, and the response template into reference files so the SKILL.md body stays a lean overview with one-level-deep links.

DimensionReasoningScore

Conciseness

The body is mostly efficient and avoids explaining concepts Claude already knows, but the overlapping 'Quick Check' and 'Audit-Ready Commands' sections and generic boilerplate (Output Requirements, Response Template, Error Handling) add length that could be trimmed.

3 / 5

Actionability

The audit CLI commands (py_compile, --help, --text) are executable, but the Core Capabilities code references a non-existent module (scripts/consent_simplifier) and methods (simplify_section, clarify_risks, assess_readability, check_compliance) that do not exist in the bundled scripts/main.py, so the primary examples are not executable against the real bundle.

3 / 5

Workflow Clarity

A clear 10-step sequence includes two explicit checkpoints, a readability feedback loop, a compliance check, a fallback, and a required-elements checklist, though several validation steps rely on user confirmation rather than concrete automated checks.

4 / 5

Progressive Disclosure

Sections are clearly labeled, but the ~200-line body is monolithic with no reference files for content that could be split out, and it references a non-existent scripts/consent_simplifier.py instead of the real scripts/main.py, producing an inaccurate reference path.

3 / 5

Total

13

/

20

Passed

Description

63%Weight 40%Scale 1-5

Based on the skill's description, can an agent find and select it at the right time? Clear, specific descriptions lead to better discovery.

The description is specific and well-scoped to a clear regulatory niche, but it omits any explicit trigger guidance and leans on technical jargon over the natural phrases a user would say. Adding a 'Use when…' clause with layperson trigger terms would lift the completeness and trigger-term dimensions.

Suggestions

Add an explicit 'Use when…' clause with trigger phrases such as 'simplify consent', 'plain language consent form', or 'patient-friendly consent form'.

Replace or supplement regulatory jargon (FDA 21CFR50/ICH-GCP/HIPAA) with natural synonyms a patient-facing user would actually say.

Keep the concrete capability list but trim the acronym-heavy tail so the description reads as triggers rather than a compliance spec.

DimensionReasoningScore

Specificity

Lists multiple concrete actions — simplification of consent documents, readability assessment at a target grade level, risk/benefit clarification in table format, and FDA/ICH-GCP/HIPAA compliance validation — giving comprehensive coverage of capabilities.

5 / 5

Completeness

Clearly states what the skill does but provides no 'Use when…' clause or equivalent trigger guidance, which caps completeness at 3 per the rubric guidelines.

3 / 5

Trigger Term Quality

Contains some natural terms ('informed consent documents', 'patient-friendly language') but is heavy on regulatory jargon (FDA 21CFR50/ICH-GCP/HIPAA) and omits common variations users would say such as 'simplify consent' or 'plain language consent'.

3 / 5

Distinctiveness Conflict Risk

Targets a narrow niche (consent simplification with regulatory compliance) that is mostly distinct, though it could overlap with general medical plain-language skills and lacks explicit distinct trigger phrases.

4 / 5

Total

15

/

20

Passed

Validation

87%

Checks the skill against the spec for correct structure and formatting. All validation checks must pass before discovery and implementation can be scored.

Validation14 / 16 Passed

Validation for skill structure

CriteriaDescriptionResult

frontmatter_unknown_keys

Unknown frontmatter key(s) found; consider removing or moving to metadata

Warning

referenced_paths_exist

Referenced path issues: 2 missing

Warning

Total

14

/

16

Passed

Repository
aipoch/medical-research-skills
Reviewed

Table of Contents

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