## RCT vs. Quasi-Experimental Design **Key Point:** The defining feature of an RCT is **random allocation** of participants to intervention and control groups. This single feature is what elevates an RCT to the gold standard and distinguishes it from all other study designs. ### Comparison Table | Feature | RCT | Quasi-Experimental | Observational | |---------|-----|-------------------|---------------| | **Random allocation** | ✓ Yes | ✗ No | ✗ No | | Control group | ✓ Yes | ✓ Yes | ✗ Often no | | Baseline measurement | ✓ Yes | ✓ Yes | ✓ Yes | | Objective outcomes | ✓ Yes | ✓ Yes | ✓ Yes | | Establishes causation | ✓ Yes | ✗ Limited | ✗ No | **High-Yield:** Quasi-experimental designs (before-after, interrupted time series, non-randomized controlled trials) have all the trappings of an RCT *except* random allocation. This lack of randomization leaves them vulnerable to selection bias and confounding. ### Why Randomization is Critical 1. **Eliminates selection bias** — participants cannot self-select into groups 2. **Balances unknown confounders** — unlike matching or stratification, which only control known factors 3. **Enables causal inference** — the only systematic difference between groups is the intervention **Clinical Pearl:** A study with a control group, baseline and follow-up measurements, and objective outcomes but *no* randomization is still vulnerable to bias if sicker patients preferentially choose one treatment. **Mnemonic: RCT = R** — **R**andom allocation is the **C**ritical **T**rait.
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