CausalSmith · seminar slides
Variance After Random Group Formation
When groups compete for members of a finite population, standard cluster variance calculations can exceed the variance of the estimated treatment effect.
slides for Random Group Formation and the Equal-group CR2 Variance in Finite Populations
Motivation
- A population of n units supplies Gn disjoint groups, each of fixed size M≥2.
- Treatment is randomized across groups. Outcomes may depend on who joins each group.
- We want the average treatment effect across possible group compositions—and its variance over repeated grouping and assignment.
- The participating population has size Nn=MGn. Drawing one group changes the members available to every other group.
Fu et al. (2026), our closest comparison, establish CR2 ratio consistency under boundedness, their other assumptions, and the sparse condition Nn2/n→0.
What happens when competition for members remains relevant?
Standard Approach
Compare treated and control group means, then use a cluster-robust variance estimator with the CR2 small-sample adjustment.
Let G1n and G0n be the treated and control group counts. Let sz,n2 be the sample variance of observed group means in arm z, using denominator Gzn−1.
VCR2,n=G1ns1,n2+G0ns0,n2.
This adds the estimated variance of each arm mean.
Pustejovsky and Tipton (2018) develop the adjustment under an independent-cluster working covariance model. Disjoint random groups can covary because they cannot reuse members.
When does this calculation still recover the exact design variance?
Key Idea
Keep the covariance created by drawing groups without replacement.
Separate treatment-effect variation into additive member contributions and remaining composition effects. Only the additive part survives in the leading finite-population correction.
With fixed group size, growing group count, stable treatment shares, convergent participation, and bounded outcomes:
- CR2 estimates the independent-group variance scale.
- The exact variance subtracts participation density times additive treatment-effect heterogeneity.
With a positive scaled-variance floor, CR2 is asymptotically conservative; it is sharp exactly when that correction is relatively negligible.
Example
Eight units form four pairs; two pairs receive treatment. All units participate.
Four units have sign ai=+1, and four have sign ai=−1. For pair A={j,k}, both members have potential outcomes
Yi,n(0,A)=0,Yi,n(1,A)=2aj+ak.
The treated pair outcome is its average sign. Selecting a pair with positive signs removes those signs from the remaining pool.
The exact variance of the treated–control difference is σn2=1/7, but
E[VCR2,n]=72.
Expected CR2 is twice the exact variance. Which feature of the outcome table creates this gap?
Model
Draw the disjoint groups uniformly, then independently choose exactly G1n groups for treatment.
For arm z∈{0,1}, Yi,n(z,A) is unit i's fixed potential outcome in group A. The group table records its average:
hz,n(A)=M1i∈A∑Yi,n(z,A).
Our target averages the treatment contrast over every possible size-M group; En denotes that uniform average:
τn=En[h1,n−h0,n].
For realized group Ang, let Zng=1 indicate treatment. The estimator is
τn=G1n1g∑Zngh1,n(Ang)−G0n1g∑(1−Zng)h0,n(Ang).
It is unbiased for τn. Its exact variance, σn2, includes both grouping and treatment randomness.
Assumptions
Consider feasible experiments with fixed group size M≥2 and deterministic potential outcomes.
- Group growth: Gn→∞, providing many randomized groups.
- Stable treatment shares: pn=G1n/Gn→p∈(0,1), keeping both arms represented.
- Convergent participation: Nn/n→ρ∈[0,1], recording how much of the population participates.
- Bounded outcomes: supn,i,z,A∣Yi,n(z,A)∣≤B<∞, ruling out increasingly extreme outcomes.
- Variance floor: cσ≤liminfn→∞Gnσn2, with cσ>0, preventing the target variance from vanishing too quickly.
The pair-sign example has B=1 and full participation. It illustrates the finite mechanism; the asymptotic results require growing group counts.
Additive Heterogeneity
For a group table f, its additive component has the form Πn,1f(A)=∑i∈Abi, with centered member coefficients ∑i=1nbi=0.
Each bi measures a member's additive contribution to the centered group outcome.
The remaining centered table, f−Enf−Πn,1f, is orthogonal to every centered additive sum: their product averages to zero over possible groups. This distinguishes member contributions from residual composition effects.
For the treatment-contrast table, define
Eτ,1,n=∥Πn,1(h1,n−h0,n)∥n2.
The squared norm means average squared additive contrast over possible groups.
In the pair-sign example, bi=ai/2. The contrast is entirely additive, the residual is zero, and Eτ,1,n=V1,n=3/7, where V1,n is the treated-table variance.
Main Result
Let Vz,n be the variance of arm z's outcome table over all possible groups. The independent-group variance scale is
Rn=pnV1,n+1−pnV0,n.
Under group growth, stable treatment shares, convergent participation, and bounded outcomes,
Gnσn2−(Rn−ρEτ,1,n)→0,
The exact variance, scaled by group count, subtracts the participation-weighted additive contrast variation.
With the variance floor as well,
GnVCR2,n−Rnp0
CR2 tracks Rn, rather than the corrected scale. Neither scale needs to converge to a constant.
Why does dependence change the exact variance while leaving CR2's target intact?
Exact Variance
Let Cab,n be the covariance between arm-a and arm-b outcomes for a uniformly drawn disjoint pair of groups.
Their treatment-contrast covariance is Cττ,n=C11,n+C00,n−2C10,n.
For a feasible design with at least two groups per arm,
σn2=GnRn+Cττ,n−G1nC11,n−G0nC00,n,
The within-arm sample variances incorporate the final two terms. Their expected CR2 calculation misses exactly the contrast covariance:
E[VCR2,n]−σn2=−Cττ,n.
In the pair-sign example, Cττ,n=C11,n=−1/7. Its negative covariance explains the entire expectation gap of 1/7.
Removing Members
For a group table f, Knf averages its value over groups disjoint from an already chosen group A:
(Knf)(A)=(Mn−M)−1C:C∩A=∅∑f(C).
The Johnson decomposition separates the centered table into mutually orthogonal components Πn,kf: degree one is additive; higher degrees contain composition variation left after lower degrees are removed. We use the decomposition of Filmus (2016).
Disjointness multiplies each component separately:
Kn(Πn,kf)(A)=λn,kΠn,kf(A),λn,k=(−1)k(n−M)k(M)k,
Here k is the degree and (x)k is a falling factorial.
For degree one, λn,1=−M/(n−M): an above-average additive group leaves a below-average pool.
Accumulating Dependence
Orthogonality turns the treatment-contrast covariance into a sum of separate degree contributions:
Cττ,n=k=1∑Mλn,kΠn,k(h1,n−h0,n)n2.
Each component contributes its mean square times its disjointness multiplier.
- Degree one: multiplying −M/(n−M) by Gn leaves the participation correction.
- Higher degrees: their multipliers decay faster. Bounded outcomes control total component variation; their combined contribution after scaling by Gn has absolute value at most C/n, for a constant C.
Thus
GnCττ,n+ρEτ,1,n→0,
The scaled contrast covariance approaches minus the participation-weighted additive energy. The within-arm covariance terms in the scaled exact variance also vanish.
This gives the corrected variance scale. Does it also explain concentration of the observed sample variances?
Concentration Despite Dependence
Yes: apply the same disjointness covariance control to both the outcome table hz,n and its square hz,n2.
With fixed M, every nonconstant disjointness multiplier tends to zero. Bounded outcomes keep the total component variation bounded—for the outcome table and for its square. Their disjoint-pair covariances therefore vanish.
For each arm:
- The variance of an empirical moment has a single-group contribution divided by the growing arm count, plus a disjoint-pair covariance contribution. Both vanish.
- Consequently, empirical first and second moments concentrate around Enhz,n and En[hz,n2].
- Sample variance is second moment minus squared first moment, with a denominator adjustment tending to one. Hence sz,n2−Vz,np0.
Stable treatment shares then yield
GnVCR2,n−Rnp0
Dependence vanishes for moment estimation, but accumulates in the estimator's variance after scaling by Gn.
Conservativeness and Sharpness
Under all five assumptions, the correction is nonnegative and the variance floor permits comparison in relative terms. For every fixed tolerance ε>0,
Pr{VCR2,n/σn2<1−ε}⟶0,
The probability of understating exact variance by a fixed proportion vanishes.
informal · Theorem T-4 With fixed M≥2, group growth, stable treatment shares, convergent participation, bounded outcomes, and a positive scaled-variance floor, CR2 is ratio consistent exactly when the correction is relatively negligible.
Precisely, the ratio converges in probability to one if and only if
Rn−ρEτ,1,nρEτ,1,n⟶0.
The numerator is the correction; the denominator is the corrected variance scale.
At ρ=0, ratio consistency follows. This includes Nn=M⌊Mn3/4⌋, where Nn/n→0 although Nn2/n→∞, beyond Fu et al. (2026)'s sparsity condition.
Invisible Counterfactual Alignment
Can one realization reveal the correction? Compare two ways to draw bounded potential-outcome schedules:
- Same signs: each unit receives a fair sign, +1 or −1, shared by both arms.
- Independent signs: each unit receives independent fair signs for its two arms.
Outcomes depend only on a unit's assigned-arm sign. Each observed unit reveals one sign, so the two observed-data mixtures are identical.
Yet the scaled exact variances approach different limits:
dsame=Mp(1−p)1,dind=Mp(1−p)1−M2ρ,
These symbols name the same-sign and independent-sign variance limits.
Under same signs, the contrast energy approaches zero; under independent signs, it approaches 2/M. At ρ>0, unobserved cross-arm alignment therefore changes variance by 2ρ/M without changing the observed-data mixture.
One-realization Lower Bound
Let Cdense contain feasible sequences satisfying our five assumptions with fixed parameters M,p,ρ,B,cσ.
Require ρ>0, B≥1, and 0<cσ<dind.
informal · Theorem T-9 Under these conditions, every variance statistic based on one realization has a limiting worst-case relative-error probability of at least 1/2 at some fixed positive tolerance.
Let On contain realized groups, assignments, and observed unit outcomes. Every variance statistic Sn(On) satisfies, for some ε>0,
21≤n→∞liminfY∈CdensesupYPr(σn2Sn(On)−1>ε).
Here PrY is randomization probability for fixed potential outcomes Y.
The sign constructions concentrate on schedules in this class. Their variance targets stay separated while their observed laws remain asymptotically indistinguishable. A statistic cannot reliably hit both targets.
Open Questions
- Gaussian approximation, studentized testing, and Wald coverage.
- Finite-sample CR2 conservativeness.
- Extensions to variable group sizes.
Takeaways
- Groups compete for finite-population members. Additive member contributions create the dependence that survives at the leading variance scale.
- CR2's sample variances concentrate around population table variances. The exact design variance subtracts participation density times additive treatment-effect variation.
- Under our assumptions, CR2 is asymptotically conservative and sharp exactly when that correction is relatively negligible. At positive density, one realization cannot uniformly recover exact variance over the bounded schedule class.
Appendix: Exact Variance
This statement gives unbiasedness, the exact design variance, and the exact expectation gap for equal-group CR2.
Let n,M,Gn,G1n be natural numbers and let G0n=Gn−G1n. Suppose that:
- (Feasible partition.) The two-stage random partition design in Definition P-1 is feasible: MGn≤n.
- (Group sizes.) 2≤M, 2≤G1n, and 2≤G0n.
- (Potential outcomes.) Yi,n(z,A) is a deterministic potential-outcome schedule, defined for every A∈Ωn,M, every i∈A, and every z∈Z.
Set Vz,n=VarA∼Unif(Ωn,M){hz,n(A)},Cab,n=EAEC∣C∩A=∅[ha,n∘(A)hb,n∘(C)], and Cττ,n=C11,n+C00,n−2C10,n,Rn=G1n/GnV1,n+1−G1n/GnV0,n. For the difference-in-means estimator τn, the finite-population PAME τn, the exact design variance σn2=Var(τn), and the scalar equal-group CR2 statistic VCR2,n in Definition P-7, E[τn]=τn, σn2=GnRn+Cττ,n−G1nC11,n−G0nC00,n, E[VCR2,n]=G1nV1,n−C11,n+G0nV0,n−C00,n, and E[VCR2,n]−σn2=−Cττ,n.
Appendix: Dense Projection Limit
This statement identifies the degree-one finite-population correction and bounds the aggregate higher-degree contribution.
Fix a common group size M≥2 and real numbers p, ρ, and B. There is a constant C>0 such that, for every feasible triangular schedule array with common group size M and every rowwise choice of Johnson projections Πn,k on L2(Ωn,M), the following conditions imply the displayed limits below:
- (Group growth.) The array satisfies Assumption A-1.
- (Treatment fractions.) The array satisfies Assumption A-2 with limiting treated-group fraction p.
- (Sampling fractions.) The array satisfies Assumption A-3 with limiting grouped-unit fraction ρ.
- (Bounded outcomes.) The array satisfies Assumption A-4 with uniform outcome envelope B.
- (Johnson decomposition.) In every row with 2M≤n, the projections give the centered orthogonal Johnson decomposition k=1∑MΠn,kf(A)=f(A)−Enf for every f and every A∈Ωn,M, and distinct Johnson degrees are orthogonal under ⟨⋅,⋅⟩n.
- (Kneser spectrum.) In every row with 2M≤n, every f∈Hn,k is an eigenfunction of the unnormalized Kneser adjacency operator with eigenvalue (−1)k(M−kn−M−k).
Then Gnσn2−(Rn−ρEτ,1,n)→0, GnCττ,n+ρEτ,1,n→0, and pnC11,n+1−pnC00,n→0. Moreover, for every row n, the pooled contribution of Johnson degrees k≥2, Gnk=2∑Mλn,kΠn,k(h1,n−h0,n)n2, has absolute value at most C/n.
Appendix: CR2 Phase Frontier
This statement gives CR2's probability limit, its one-sided conservativeness, and the necessary and sufficient condition for ratio consistency.
Let M≥2, and let A be a triangular array of feasible random-group experiment rows with population sizes n, group counts Gn>0, treated-group counts 0<G1n<Gn, grouped-unit counts Nn=MGn≤n, and deterministic potential-outcome schedules. Fix constants p,ρ,B,cσ∈R. Suppose that:
- (Dense array.) The array A belongs to the dense bounded schedule class Cdense in Definition P-8, with parameters p,ρ,B,cσ.
- (Johnson projections.) For every row n, the spaces L2(Ωn,M) are equipped with linear projections Πn,k, 0≤k≤M, whose ranges are the degree-k Johnson harmonic subspaces Hn,k, which fix functions in their ranges and have residuals orthogonal to Hn,k under ⟨⋅,⋅⟩n.
- (Orthogonal decomposition.) For every row with 2M≤n, every f∈L2(Ωn,M), and every A∈Ωn,M, k=1∑MΠn,kf(A)=f(A)−Enf, and distinct Johnson components are orthogonal: ⟨Πn,kf,Πn,ℓg⟩n=0whenever k=ℓ.
- (Kneser spectrum.) For every row with 2M≤n, every 0≤k≤M, and every f∈Hn,k, the unnormalized Kneser adjacency operator satisfies C∩A=∅∑f(C)=(−1)k(M−kn−M−k)f(A).
Then, as n→∞, GnVCR2,n−Rnp0 and Gn(VCR2,n−σn2)−ρEτ,1,np0. Moreover, for every ε>0, Pr{VCR2,n/σn2<1−ε}⟶0, and the ratio VCR2,n/σn2 converges in probability to 1 if and only if Rn−ρEτ,1,nρEτ,1,n⟶0.
Appendix: One-realization Lower Bound
This statement proves a nonvanishing worst-case relative-error probability for every one-realization variance statistic at positive density.
Fix a common group size M with 2≤M, and let A be a triangular schedule array with population sizes n, group counts Gn>0, treated-group counts 0<G1n<Gn, MGn≤n, and deterministic potential-outcome rows. Let p,ρ,B,cσ∈R. Suppose:
- (Envelope and fractions.) 0<ρ, 1≤B, and the array satisfies Assumption A-1, Assumption A-2, Assumption A-3 with limiting treated-group fraction p and limiting grouped-unit fraction ρ.
- (Johnson decomposition input.) For every row n, there are orthogonal projections Πn,k onto the degree-k Johnson harmonic spaces Hn,k, k=0,…,M, whose positive-degree components give the centered orthogonal decomposition of every f∈L2(Ωn,M): k=1∑MΠn,kf=f−Enf,⟨Πn,kf,Πn,ℓg⟩n=0for k=ℓ.
- (Kneser spectrum input.) For every row n with 2M≤n, the Kneser adjacency operator acts on f∈Hn,k by the eigenvalue (−1)k(M−kn−M−k),k=0,…,M.
- (Variance lower bound.) With dsame=Mp(1−p)1,dind=Mp(1−p)1−M2ρ, the constant cσ satisfies 0<cσ<dind.
Then there exist support sets Γnsame for the common-arm Rademacher prior Hnsame and Γnind for the independent-arm Rademacher prior Hnind such that both prior probabilities tend to one, every diagonal selection from either support induces an array in Cdense with parameters (p,ρ,B,cσ), the conditioned one-realization laws satisfy TV(Hnsame(On∈⋅∣Γnsame),Hnind(On∈⋅∣Γnind))→0, and the scaled exact variances converge uniformly on the respective supports: u∈ΓnsamesupGnσn2(u)−dsame→0,u∈ΓnindsupGnσn2(u)−dind→0. Moreover, there is an ε>0 such that every measurable one-realization variance statistic Sn(On) satisfies 21≤n→∞liminfY∈CdensesupYPr(σn2Sn(On)−1>ε).