Results for “clinical-research”

Design prospective clinical studies by selecting and classifying endpoints, estimating sample size and power for two-arm designs, and scoring study plans for feasibility with phase-gate decisions.

Draft an internal legal research memo for the supervising attorney with verified authority and flagged open questions.

Generate comprehensive clinical reports including case reports (CARE guidelines), diagnostic reports, clinical trial reports (ICH-E3, SAE, CSR), and patient documentation (SOAP, H&P, discharge summaries) with templates, regulatory compliance, and validation tools.

Evidence-based health research using tiered trusted sources with GRADE-inspired evidence ratings. Integrates Apple Health data for personalized context. Use when user asks health, nutrition, exercise, sleep, or wellness questions.

NIH grant research skill for clinical researchers. Grill-me intake (research idea + career stage + preliminary data + environment + submission posture + known institute targets) locks down the funding strategy before any search runs. Runs a 5-face...

进行市场研究、竞争分析、投资者尽职调查和行业情报，附带来源归属和决策导向的摘要。适用于用户需要市场规模、竞争对手比较、基金研究、技术扫描或为商业决策提供信息的研究时。

Transparent, rigorous research with full methodology — not a black-box API wrapper. Conducts exhaustive investigation through mandated 2-cycle research per theme, APA 7th citations, evidence hierarchy, and 3 user checkpoints. Self-contained using native OpenClaw tools (web_search, web_fetch, sessions_spawn). Use for literature reviews, competitive intelligence, or any research requiring academic rigor and reproducibility.

Evidence-first current-state research workflow for ECC. Use when the user wants fresh facts, comparisons, enrichment, or a recommendation built from current public evidence and any supplied local context.

Research a customer question across docs, changelogs, and past tickets, then answer with source attribution, a confidence rating, and honest gaps.

Evaluate scientific claims and evidence quality by assessing experimental design, identifying biases and confounders, and applying evidence grading frameworks like GRADE and Cochrane Risk of Bias.

Generate novel research ideas through structured, conversational brainstorming that explores interdisciplinary connections, challenges assumptions, and identifies research gaps.

Generate structured research briefs from RSS feeds and web sources on any topic. Synthesizes multiple sources into actionable analysis with key findings, data points, expert perspectives, and content angles.

Runs evidence-first research workflows by combining search, synthesis, and recommendation skills for current facts, comparisons, or enrichment.

Discovers and uses scientific datasets, models, blog posts, and interactive demos from a curated catalog for AI/ML work in domains like biology, chemistry, physics, and genomics.

Query the ClinPGx API for pharmacogenomic gene-drug data, clinical annotations, CPIC guidelines, and FDA drug labels.

Queries the ClinPGx REST API for pharmacogenomic gene-drug data, clinical annotations, CPIC guidelines, and FDA drug labels, generating markdown reports with CSV tables.

Runs evidence-first research workflows, choosing the lightest useful path from search to deep synthesis, and labels facts, inference, and recommendations.

Produces decision-oriented market research, competitive analysis, investor due diligence, and industry intelligence with source attribution.

Runs evidence-first current-state research, comparing options and enriching people or companies, then reports with explicit evidence boundaries.

Research companies, industries, or competitor sets using web search and seven analytical lenses to produce structured intelligence for downstream product management tasks.

Plan and synthesize product/user research with method rigor: select the right method for the goal, compute defensible sample sizes with confidence labels, and cluster coded observations into insights while flagging single-source anecdotes.

Route research prompts to evidence, retrieval, scraping, data, market, or scientific research skills. Use when prompts mention deep research, current facts, citations, Exa, iterative retrieval, search-first, scraping, data pipelines, PubMed, USPTO, gget, literature review, or scholar evaluation.

以证据为先的ECC当前状态研究工作流程。当用户希望基于当前公开证据和提供的本地上下文获取最新事实、比较、丰富信息或建议时使用。

Research external tools/competitors for a topic and write findings to BRAINSTORM.md (project topics) or ~/.clade/research/ (personal topics). Use when user says "/research [topic]".

Deep research on a topic using web search, docs, and codebase analysis

Use to confirm clinical ethics and research-integrity requirements for an NEJM submission — IRB/ethics-committee approval and informed consent per the Declaration of Helsinki, ICMJE conflict-of-interest disclosures and authorship criteria, the role-of-the-funding-source statement, and the ICMJE data-sharing statement.

Conduct multi-pass web and academic research, cross-check claims, and produce a cited report saved to file and memory.

Researches VC funds and partners, providing thesis matching, portfolio analysis, and approach strategy for outreach.

Build detailed ideal customer profiles with pain points, objections, buying triggers, and messaging angles. Includes community research to find where ICPs gather online and extract their exact language. Use when researching audiences, creating buyer personas, or developing targeted messaging.

Conducts Privacy Impact Assessment for health data processing under GDPR Article 9, HIPAA, and sector-specific health privacy regulations. Covers special category data safeguards, clinical research data, patient portals, health wearables, genetic data, and cross-border health data transfers. Keywords: health data PIA, DPIA, Article 9, HIPAA, special category data, clinical research, patient privacy, genetic data.

Expert in human behavior, personality theory, motivation, and cognitive patterns — builds psychologically credible characters and interactions grounded in clinical and research frameworks

Guides DPIA for health and medical data processing covering Art. 9(2)(h)-(j) exemptions, HIPAA crosswalk for transatlantic operations, clinical trial data protection under EU CTR 536/2014, and genetic data specifics under Art. 9(1). Activate for healthcare systems, clinical research, health apps, or medical device data. Keywords: health data, DPIA, Art. 9, clinical trial, genetic data, HIPAA, medical records, special category.