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Related Subjects: |Basic Statistics |Sampling in Medical Statistics |Reading a Medical paper |Different Forms of Medical Trials and Studies |Hierarchy of Evidence-Based Trials |Bayes' Theorem |Comparing Groups
Sampling is a fundamental aspect of medical statistics, enabling researchers to draw conclusions about a population based on a subset of that population. Effective sampling methods are crucial for ensuring that the sample accurately represents the population, allowing for valid and reliable inferences.
📊 Sampling is the process of selecting a subset (sample) from a larger population to make inferences about the whole group. In medical research, robust sampling ensures generalisability, reduces bias, and supports evidence-based decisions in clinical trials, epidemiology, and public health. Probability sampling remains the gold standard for unbiased inference; non-probability is useful for exploratory, hard-to-reach, or resource-limited studies.
| Type | Subtype | Description | Strengths | Limitations | Medical Example |
|---|---|---|---|---|---|
| Probability Sampling (each unit has known, non-zero chance of selection; preferred for inference) | Simple Random | Random selection from full population list (e.g., random number generator). | Unbiased, easy to analyse statistically. | Requires complete sampling frame; may miss subgroups. | Randomly select patients from hospital database for drug trial. |
| Stratified | Divide population into strata (e.g., age, sex), then random sample proportionally or equally from each. | Ensures subgroup representation; ↑ precision. | Needs accurate strata data. | RCT stratified by disease severity and centre. | |
| Cluster | Randomly select clusters (e.g., clinics), then sample all or randomly within clusters. | Cost-effective for geographically dispersed populations. | Intra-cluster correlation reduces effective sample size. | Vaccine trial in randomly selected villages (all residents sampled). | |
| Systematic | Select every nth unit after random start (e.g., every 10th patient). | Simple, even spread. | Risk of periodicity bias if list ordered. | Survey every 5th patient in waiting room. | |
| Multistage | Combine methods (e.g., cluster → stratified → random). | Practical for large/national studies. | Complex design effect. | NHANES: counties → segments → households → individuals. | |
| Non-Probability Sampling (no known selection probability; useful exploratory, qualitative, rare diseases) | Convenience | Sample easily accessible subjects. | Fast, cheap. | High selection bias; poor generalisability. | Recruit volunteers at clinic for pilot study. |
| Purposive / Judgmental | Researcher selects based on expertise (e.g., typical cases, experts). | Targeted, informative for specific questions. | Subjective; bias risk. | Select severe cases for rare disease phenotyping. | |
| Snowball | Initial subjects recruit peers (chain referral). | Accesses hidden/hard-to-reach populations. | Homophily bias; not representative. | Recruit PWID for hepatitis C study via networks. | |
| Quota | Set quotas for subgroups (e.g., age/gender) then non-random fill. | Ensures diversity; quick. | Non-random within quotas → bias. | Survey equal men/women in different age bands for health attitudes. |
| Bias Type | Description | Mitigation in Medical Research |
|---|---|---|
| Selection Bias | Sample not representative (e.g., hospital-only) | Use probability sampling; randomisation in trials; oversample underrepresented groups. |
| Non-response Bias | Non-responders differ systematically | High response rates, follow-up reminders, imputation, sensitivity analyses. |
| Volunteer Bias | Volunteers healthier/more motivated | Recruit consecutively; use registries; compare responders/non-responders. |
| Survivor Bias | Only survivors included | Intention-to-treat analysis; capture all eligible; adjust for loss to follow-up. |
| Channeling Bias | Treatment allocation based on prognosis | Randomisation + blinding; propensity score matching in observational studies. |
Teaching Point 🩺 Probability sampling (random, stratified, cluster) → unbiased, generalisable results (gold standard for inference). Non-probability (convenience, purposive, snowball) → quick, targeted, but limited generalisability. Sample size: Balance precision (margin of error), power (80–90%), effect size, and feasibility. Bias mitigation: Randomisation, stratification, high response rates, sensitivity analyses. Report sampling method transparently (STROBE/CONSORT); consider design effect in clusters.