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The Synthetic Control Method

When no single untreated unit is a good comparison, build a weighted blend of several untreated units, a 'synthetic' version of the treated unit, that matches its pre-treatment history closely, and use its post-treatment path as the counterfactual.

Prerequisites: Parallel Trends and Pre-Trend Tests

A single exchange changes its tick-size rules and an analyst wants to know the effect on trading volume. There's no other exchange that's a close match on its own, one is too small, another trades a different mix of instruments, a third has different market hours. No individual comparison exchange is a fair control. The synthetic control method's insight: don't pick one imperfect comparison, build a custom blend of several imperfect comparisons, weighted so the blend's pre-change history tracks the treated exchange closely, and let that blend's post-change path stand in for what would have happened without the rule change.

An analogy: mixing a paint color you don't have

You need a specific shade of green paint but the store only sells blue, yellow, and a slightly-off green. Instead of using any one can as an imperfect substitute, you mix a custom blend, 40% blue, 35% yellow, 25% off-green, that matches your target shade as closely as possible when tested on a swatch you can already see (the "pre-treatment" period). Once you're confident the blend matches on the swatch you can check, you trust the same blend recipe to tell you what the color would look like on a wall you haven't painted yet (the "post-treatment" period), the mixing weights, not any single can, are what does the work.

The method, one symbol at a time

Let Y1tY_{1t} be the treated unit's outcome at time tt, and YjtY_{jt} the outcome for each of JJ untreated "donor" units. Choose non-negative weights wjw_j summing to 1 that minimize the gap between the treated unit and the weighted blend during the pre-treatment period t<T0t < T_0:

minw1,,wJ0,  wj=1t<T0(Y1tj=1JwjYjt)2\min_{w_1,\dots,w_J \ge 0,\; \sum w_j = 1} \sum_{t < T_0} \left( Y_{1t} - \sum_{j=1}^{J} w_j Y_{jt} \right)^2

In plain English: find the combination of donor units, using only nonnegative weights that add to one, so it's a genuine weighted average, never an extrapolation beyond the data, that best reproduces the treated unit's own history before the change. The estimated treatment effect at any later time tT0t \ge T_0 is simply:

τ^t=Y1tj=1JwjYjt\hat{\tau}_t = Y_{1t} - \sum_{j=1}^{J} w_j Y_{jt}

the treated unit's actual outcome minus what the synthetic blend (extended forward using the same weights) would predict.

Worked example 1: constructing the blend

Suppose three donor exchanges have pre-change monthly volumes (in $bn) over three months: Donor A: 10, 11, 12. Donor B: 6, 5, 7. Donor C: 20, 19, 21. The treated exchange: 12.8, 12.7, 13.9. Solving the weighting problem might yield wA=0.5w_A = 0.5, wB=0.3w_B = 0.3, wC=0.2w_C = 0.2 (illustrative, found by minimizing squared pre-period gaps): synthetic path =0.5(10,11,12)+0.3(6,5,7)+0.2(20,19,21)=(5+1.8+4,5.5+1.5+3.8,6+2.1+4.2)=(10.8,10.8,12.2)= 0.5(10,11,12) + 0.3(6,5,7) + 0.2(20,19,21) = (5+1.8+4, 5.5+1.5+3.8, 6+2.1+4.2) = (10.8, 10.8, 12.2), reasonably close to but not exactly matching (12.8, 12.7, 13.9); in practice you'd refine weights further, but this illustrates the mechanics: the blend tracks the shape of the treated unit's history using only real donor data.

Worked example 2: reading the post-treatment gap

Suppose after refinement the synthetic blend tracks the treated exchange near-exactly pre-change (gap under 0.1 every month), and the tick-size rule changes in month 4. Post-change: treated exchange volume is 11.5, while the synthetic blend (same weights, extended using donors' actual month-4 volumes) is 13.6. The estimated effect is τ^4=11.513.6=2.1\hat\tau_4 = 11.5 - 13.6 = -2.1, i.e., roughly a $2.1bn reduction in monthly volume attributable to the rule change. Because the pre-period fit was tight, this gap is much more credible than it would be if the synthetic blend had only loosely tracked the treated exchange beforehand, the tightness of the pre-period fit is itself the evidence for (or against) trusting the post-period gap.

rule change ─ treated exchange - - synthetic blend gap = effect
The synthetic blend (dashed) is constructed to track the treated unit (solid) tightly before the rule change; the widening gap after the change is the estimated treatment effect.
w=0.5 Donor A w=0.3 Donor B w=0.2 Donor C
The weights are chosen purely to match pre-treatment history as closely as possible, they are not judgment calls, and every weight is non-negative and the three sum to one.

What this means in practice

Synthetic control is the standard tool when you have exactly one (or very few) treated units and a panel of untreated candidates, none of which alone is a convincing match, a common situation for exchange-level or country-level policy changes where randomization was never possible and there's no natural single control group. It shares difference-in-differences' reliance on a parallel-trends-style assumption, but instead of assuming it holds for one chosen control, it constructs a control specifically engineered to satisfy it, and the tightness of the pre-period fit is a direct, visible diagnostic of how much to trust the result, unlike diff-in-diff, where a poor implicit match is easy to overlook.

Synthetic control builds a weighted blend of several untreated donor units, chosen to closely reproduce the treated unit's own pre-treatment history, and then uses the gap between the treated unit and that blend after treatment as the estimated causal effect.

A tight pre-treatment fit is necessary but can be achieved almost by construction if you allow too many donor units or too flexible a weighting scheme relative to how few pre-treatment periods you have, with enough donors and only a handful of pre-periods, you can nearly always find some weighted blend that fits well, whether or not the blend represents a meaningful counterfactual. Always check that the fit isn't simply overfit to a short pre-period, for example via placebo tests that apply the same method to untreated units and confirm they don't show similarly large "effects."

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Further reading

  • Abadie, Diamond & Hainmueller, JASA 2010
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