Skip to main content

experiment-design

Design scientific experiments including sample size calculation, randomization, control groups, blinding, and study protocols. Covers RCTs, quasi-experiments, factorial designs, A/B tests, survey design, and observational studies. Use when user asks to design an experiment, calculate sample size, plan a study, set up controls, or create a research protocol. Triggers on "design experiment", "sample size", "power analysis", "study design", "control group", "randomization", "A/B test", "factorial design", "survey design".

インストールへ移動

ソース情報

リポジトリ
beita6969/ScienceClaw
ソースの最終更新活動
2026年3月12日 04:53
検出された SKILL.md の言語
英語
スター
907
フォーク
104

インストール方法

デフォルトでは、最初にソースを確認する Prompt が選択されています。直接コマンドに切り替えるか、ローカルコピーをダウンロードすることもできます。

ソースファイルを確認

インストールを決める前に、SKILL.md と SkillsMP に表示されている付属ファイルをお読みください。

SKILL.md を表示中

SKILL.md
ソースの指示 · 読み取り専用プレビュー
name
experiment-design
description
Design scientific experiments including sample size calculation, randomization, control groups, blinding, and study protocols. Covers RCTs, quasi-experiments, factorial designs, A/B tests, survey design, and observational studies. Use when user asks to design an experiment, calculate sample size, plan a study, set up controls, or create a research protocol. Triggers on "design experiment", "sample size", "power analysis", "study design", "control group", "randomization", "A/B test", "factorial design", "survey design".
# Experiment Design Scientific experiment planning, power analysis, and protocol development. ## Design Selection Guide | Research Question | Recommended Design | |---|---| | Does X cause Y? | RCT (gold standard) | | Does X cause Y? (can't randomize) | Quasi-experiment, natural experiment | | How do factors interact? | Factorial design | | Which version performs better? | A/B test | | What is the prevalence/association? | Cross-sectional survey | | How does outcome change over time? | Longitudinal / cohort study | | What is the lived experience? | Qualitative (interviews, ethnography) | | Does intervention work in practice? | Pragmatic trial | ## Power Analysis & Sample Size ```python source /Users/zhangmingda/clawd/.venv/bin/activate python3 << 'EOF' from scipy import stats import numpy as np # --- Two-sample t-test --- def sample_size_ttest(effect_size, alpha=0.05, power=0.80): """Cohen's d effect sizes: small=0.2, medium=0.5, large=0.8""" from scipy.stats import norm z_alpha = norm.ppf(1 - alpha/2) z_beta = norm.ppf(power) n = 2 * ((z_alpha + z_beta) / effect_size) ** 2 return int(np.ceil(n)) # --- Chi-square test --- def sample_size_chi2(effect_size, alpha=0.05, power=0.80, df=1): """Cohen's w effect sizes: small=0.1, medium=0.3, large=0.5""" from scipy.stats import norm, chi2 z_beta = norm.ppf(power) z_alpha = norm.ppf(1 - alpha) n = ((z_alpha + z_beta) / effect_size) ** 2 return int(np.ceil(n)) # --- Correlation --- def sample_size_correlation(r, alpha=0.05, power=0.80): from scipy.stats import norm z_alpha = norm.ppf(1 - alpha/2) z_beta = norm.ppf(power) z_r = 0.5 * np.log((1+r)/(1-r)) # Fisher's z n = ((z_alpha + z_beta) / z_r) ** 2 + 3 return int(np.ceil(n)) # Examples print(f"t-test (d=0.5): n={sample_size_ttest(0.5)} per group") print(f"t-test (d=0.3): n={sample_size_ttest(0.3)} per group") print(f"Chi-square (w=0.3): n={sample_size_chi2(0.3)}") print(f"Correlation (r=0.3): n={sample_size_correlation(0.3)}") EOF ``` ## Key Design Principles ### Controls - **Positive control**: Known to produce effect (validates method works) - **Negative control**: Known to produce no effect (validates baseline) - **Placebo control**: Inert treatment (controls for expectation effects) - **Active control**: Existing standard treatment (for superiority/non-inferiority) ### Randomization - **Simple**: Coin flip / random number - **Block**: Ensures equal groups per block - **Stratified**: Randomize within strata (age, sex, severity) - **Cluster**: Randomize groups, not individuals ### Blinding - **Single-blind**: Participants don't know assignment - **Double-blind**: Participants and researchers don't know - **Triple-blind**: Participants, researchers, and analysts don't know ### Bias Mitigation | Bias | Mitigation | |------|-----------| | Selection bias | Random sampling, clear inclusion criteria | | Allocation bias | Random assignment, concealed allocation | | Performance bias | Blinding, standardized protocols | | Detection bias | Blinded outcome assessment | | Attrition bias | ITT analysis, minimize dropout | | Reporting bias | Pre-registration, analysis plan | ## Study Protocol Template ```markdown # Study Protocol: [Title] ## 1. Background & Rationale ## 2. Objectives & Hypotheses - Primary: - Secondary: ## 3. Study Design - Type: [RCT / quasi-experiment / observational / ...] - Duration: ## 4. Participants - Population: - Inclusion criteria: - Exclusion criteria: - Sample size: N = [calculated], power = 0.80, α = 0.05 ## 5. Intervention / Exposure ## 6. Outcome Measures - Primary: - Secondary: ## 7. Randomization & Blinding ## 8. Data Collection Procedures ## 9. Statistical Analysis Plan - Primary analysis: - Secondary analyses: - Handling of missing data: ## 10. Ethical Considerations - IRB/Ethics approval: - Informed consent: - Data privacy: ## 11. Timeline ## 12. Budget ``` ## Pre-registration Recommend pre-registration for confirmatory studies: - **OSF**: osf.io (general) - **ClinicalTrials.gov**: clinical trials - **PROSPERO**: systematic reviews - **AsPredicted**: aspredicted.org (quick) ## Tips - Always justify sample size with power analysis - Pre-register hypotheses and analysis plan - Plan for 10-20% attrition in sample size calculation - Document all deviations from protocol - Consider pilot study for novel methods
GitHubで見る