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The Behavioral Foundations of Default Effects: Brot-Goldberg, Layton, Vabson & Wang (2023)

Distilled · extracted by claude-sonnet-4-6 Jun 25, 2026, verified by claude-sonnet-4-6 Jun 24, 2026, extracted by gpt-6-luna Oct 4, 2026, verified by gpt-6-luna Oct 4, 2026

JEL (IAR-assigned): D91, I13, I18, I38, L65 · assigned from the abstract, not the journal

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paper-summaryhealth-insurancebehavioral-economicsdefault-effectsmedicaredifference-in-differencespanel-regressionpeer-reviewedunreplicateddata:cms-medicare

What this is. The paper’s core results, the theoretical framework distinguishing frictional from mental gap models of default-following, and the three natural-experiment designs used to test them: enough to know what was found and how, without reading all 41 pages. To replicate or extend, read the full source at the original.

Default rules in the Low-Income Subsidy (LIS) segment of Medicare Part D determine what plan a beneficiary is enrolled in, and most beneficiaries never change their default assignment. Using random assignment of new enrollees to benchmark plans and two regression discontinuity and difference-in-differences designs that exploit premium-subsidy threshold crossings, the authors show that: (i) default changes shift virtually all beneficiaries through passive reassignment, not active choice; (ii) these reassignments reduce annual drug spending by 6.4 percent on average, with losses up to 30 percent for those assigned to poorly fitting plans; and (iii) beneficiaries whose randomly assigned defaults are worst-fitting are only marginally more likely to make an active choice, even as the consumption losses grow dramatically. A variance decomposition reveals that two-thirds of variation in latent attention comes from random transitory shocks within a beneficiary over time, not from permanent friction heterogeneity. This evidence favors “mental gap” models (Handel and Schwartzstein (2018)), where attention is driven by factors unrelated to the stakes, over the “frictional” class of models used in most prior work (Handel (2013); Abaluck and Gruber (2011)). The welfare implication: optimal default policy should paternalistically match beneficiaries to their best plans, not try to incentivize active choice.

Magnitudes and significance are as reported. Locators refer to pages in the source PDF.

#ResultLocatorMagnitude
R1Only 16% of new LIS beneficiaries opt out before initial auto-enrollment; 84% passively follow their randomly assigned default. Even after 5 years, only 45% have ever made an active choiceFigure 1, p. 2727Active choice remains below 50% in every plan-fit quintile after 5 years; its relationship with plan fit is not monotonic
R2A change in default from remaining to reassignment raises plan switching by 96 percentage points, driven almost entirely by passive reassignment (93.6 pp), not active choice (2.4 pp)Table 2, p. 2734RD estimate beta = 0.960 (SE 0.001); average switching rate for controls at cutoff = 0.006
R3Reassignment default reduces annual drug spending by 6.4 percent (approximately $213 off a $3,329 control base), a non-trivial consumption lossTable 3 Panel A, p. 2738DiD coefficient: -0.064 (SE 0.004) on log drug spending; effect persists at least 24 months; robust to drug-level and class-level price normalizations
R4Worst-fitting default plans reduce drug spending by 12.6 percent, nearly 3x the 4.3 percent loss for better-fitting defaults; high-fit-variance subsamples face losses up to nearly 30 percentTable 3 Panel B, p. 2738; Table 6, p. 2747Worst-quintile interaction: -0.083 (SE 0.007); top 50% / 25% / 10% variance subsamples face total losses of -24.9% / -27.6% / -29.8%
R5Active choice propensity barely responds to the value of the default: beneficiaries assigned to worst-fitting plans are only about 1.5 pp more likely to make an active choice than those assigned to better plansTable 5 Panel B, p. 2747; Figure 7, p. 2749Worst-quintile differential: 0.015 (SE 0.002); slope of active choice vs drug consumption loss is nearly flat across the full range; ∂a/∂v^d ≈ 0
R626.5 percent of beneficiaries are “sometimes choosers” whose plan exits, far exceeding the ~4.2 percent predicted by a constant-friction frictional modelp. 2752Prior passive auto-assignees make an active choice 7.7% of the time following plan exit; prior active choosers make an active choice only 25.6% of the time - far below the ~100% predicted by a constant-friction model
R7Two-thirds of variation in latent attention is driven by within-beneficiary transitory shocks, not permanent friction differences: transitory share = 66.6%, permanent heterogeneity = 33.4%Table 7, p. 2754Observable characteristics (age, gender, race, Elixhauser index) explain only 3.2% of total attention variance; unobservable permanent heterogeneity = 30.6%; transitory shocks = 66.2%
R8Drug-spending effects persist under price normalizationTable 3 Panel A, p. 2738Drug-level price normalization: -0.050 (SE 0.004); class-level price normalization: -0.021 (SE 0.004)
R9Default reassignment reduces spending across drug categories, especially chronic drugsTable 4 Panel A, p. 2740High-value drugs: -0.062 (SE 0.005); chronic drugs: -0.078 (SE 0.005); nonchronic drugs: -0.028 (SE 0.006)
R10Prior-year covariates are balanced around the RD cutoffFigure 3, p. 2732; text p. 2731Prior-year drug spending is smooth at the discontinuity; age, female share, nondrug medical spending, and Elixhauser index show similar balance in the appendix checks
R11Active choice remains uncommon after reassignment, with estimates near five percentage pointsTable 5, p. 2747Active choice by December: 0.050 (SE 0.001) in Panel A and 0.047 (SE 0.001) in Panel B; control mean in Panel B: 0.010
R12Active-choice response stays modest in groups facing greater variation in plan fitTable 6, p. 2747Top 50% / 25% / 10% fit-variance samples: reassignment effects 0.054 (SE 0.001) / 0.049 (SE 0.002) / 0.041 (SE 0.003); worst-fit interactions 0.034 (SE 0.003) / 0.034 (SE 0.004) / 0.037 (SE 0.006)

Overall (paper’s conclusion). Beneficiaries are overwhelmingly passive in their Medicare Part D plan choices, even when that passivity generates large and immediate drug consumption losses. Because active choice is insensitive to the value of the default, the evidence fits mental gap rather than frictional models of default-following. This means that policymakers cannot incentivize their way out of passivity: optimal default design should match beneficiaries to their best outcomes, not shock them into making active choices.

Section V (pp. 2740-2743) formalizes two classes of default-following models and derives the welfare implications that distinguish them, following the taxonomy of Handel and Schwartzstein (2018).

Active choice decision. Beneficiary ii makes an active choice if and only if A(v∗,vd,c,…)≥0A(v^*, v^d, c, \ldots) \geq 0, where v∗v^* is the payoff from the best active choice, vdv^d is the payoff of the default option, and cc represents the psychic, search, or attention cost of making an active choice (p. 2741). Active choosers receive v∗−cv^* - c; passive followers receive vdv^d.

Welfare. Expected welfare is (p. 2742):

W=Pr⁡ ⁣(A(v∗,vd,c,…)≥0)⋅E[v∗−c∣A(v∗,vd,c,…)≥0]+Pr⁡ ⁣(A(v∗,vd,c,…)<0)⋅E[vd∣A(v∗,vd,c,…)<0]W = \Pr\!\bigl(A(v^*, v^d, c, \ldots) \geq 0\bigr) \cdot E\bigl[v^* - c \mid A(v^*, v^d, c, \ldots) \geq 0\bigr] + \Pr\!\bigl(A(v^*, v^d, c, \ldots) < 0\bigr) \cdot E\bigl[v^d \mid A(v^*, v^d, c, \ldots) < 0\bigr]

Differentiating with respect to the default value vdv^d yields the welfare derivative (equation 2, p. 2742):

∂W∂vd=1−a(v∗,vd,c,…)⏟benefit toinframarginalpassive agents+∂a(v∗,vd,c,…)∂vd⏟attentionelasticity×E ⁣[v∗−c−vd∣A(v∗,vd,c,…)=0]⏟value of choice formarginal agents(2)\frac{\partial W}{\partial v^d} = \underbrace{1 - a(v^*, v^d, c, \ldots)}_{\substack{\text{benefit to}\\\text{inframarginal}\\\text{passive agents}}} + \underbrace{\frac{\partial a(v^*, v^d, c, \ldots)}{\partial v^d}}_{\substack{\text{attention}\\\text{elasticity}}} \times \underbrace{E\!\bigl[v^* - c - v^d \mid A(v^*, v^d, c, \ldots) = 0\bigr]}_{\substack{\text{value of choice for}\\\text{marginal agents}}} \tag{2}

where a=Pr⁡(A≥0)a = \Pr(A \geq 0) is the aggregate share making an active choice.

The frictional vs mental gap distinction. In “frictional” models, ∂a/∂vd<0\partial a / \partial v^d < 0: agents respond to a worse default by making active choices more often (the second term in equation (2) is non-zero), so optimal policy can improve welfare by setting the default so badly that all agents switch - the “shocking default” logic of Carroll et al. (2009) and Bernheim, Fradkin, and Popov (2015). In “mental gap” models, ∂a/∂vd=0\partial a / \partial v^d = 0: active choice is driven by random attention or contextual salience, not by material stakes. The second term in equation (2) drops out, leaving ∂W/∂vd=1−a>0\partial W / \partial v^d = 1 - a > 0: welfare rises with the default value, so the optimal default maximizes vdv^d (a “smart” default matching beneficiaries to their best plan, as in Thaler and Sunstein (2008)). The paper presents this as a conditional implication of the model; it does not rule out all frictional mechanisms.

Structural model of latent attention (Section VII, p. 2752). To decompose the variation in active choice, the paper models latent attention for beneficiary ii in year tt as:

Ait=ci+kitA_{it} = c_i + k_{it}

where ci∼N(μXi,σ2)c_i \sim \mathcal{N}(\mu X_i, \sigma^2) captures permanent, beneficiary-specific drivers of attention (with observable characteristics XiX_i) and kit∼N(0,1)k_{it} \sim \mathcal{N}(0, 1) are i.i.d. transitory shocks across periods. A beneficiary makes an active choice when Ait≥0A_{it} \geq 0. Estimated by maximum likelihood on sequences of active/passive choices observed for the same beneficiary over multiple plan-exit events (Online Appendix E). The key testable implication is the share of total variance explained by kitk_{it} (transitory) versus cic_i (permanent): fixed-friction models predict a larger permanent component. The two-thirds transitory share is evidence against that prediction under the fixed-friction assumption, but does not rule out time-varying frictions or all frictional models.

The paper uses three sources of quasi-random variation within the LIS segment of Medicare Part D: initial random assignment to benchmark plans, premium-subsidy threshold crossings that change continuing beneficiaries’ defaults, and plan exits that force all enrollees to face reassignment. The stacked difference-in-differences analyses reuse the benchmark-status threshold design to measure drug-consumption and active-choice responses.

Experiment 1 - New enrollee random assignment (Section II, pp. 2726-2729). When a beneficiary first qualifies for Medicare at age 65, she is randomly assigned to a benchmark plan in her service region (stratified randomization to avoid insurer gaming). The paper plots cumulative active-choice rates over 60 months post-enrollment in the 20 percent CMS claims sample, including rates by cohort and, in the linked New York and Texas sample, by plan-fit quintile. These are descriptive rates following randomized assignment, not a difference-in-differences estimate.

Experiment 2 - Regression discontinuity in plan benchmark status (Section III, pp. 2729-2735). For continuing LIS beneficiaries enrolled by auto-assignment, the default switches from “remain in your plan” to “be randomly reassigned to a new benchmark plan” if the incumbent plan sets a year-tt premium bid just above the regional subsidy level (losing benchmark status). This provides quasi-random variation in default rules around the subsidy cutoff. The regression-discontinuity-design estimating equation is (p. 2733):

Pr⁡(Switch Plans)it=β⋅1 ⁣{Bidj(i)t−Benchmarkr(i)t>0}+γ−(Bidj(i)t−Benchmarkr(i)t)⋅1 ⁣{Bidj(i)t−Benchmarkr(i)t≤0}+γ+(Bidj(i)t−Benchmarkr(i)t)⋅1 ⁣{Bidj(i)t−Benchmarkr(i)t>0}+δXit+ϵit\Pr(\text{Switch Plans})_{it} = \beta \cdot \mathbf{1}\!\bigl\{Bid_{j(i)t} - Benchmark_{r(i)t} > 0\bigr\} + \gamma^{-} (Bid_{j(i)t} - Benchmark_{r(i)t}) \cdot \mathbf{1}\!\bigl\{Bid_{j(i)t} - Benchmark_{r(i)t} \leq 0\bigr\} + \gamma^{+} (Bid_{j(i)t} - Benchmark_{r(i)t}) \cdot \mathbf{1}\!\bigl\{Bid_{j(i)t} - Benchmark_{r(i)t} > 0\bigr\} + \delta X_{it} + \epsilon_{it}

where Bidj(i)tBid_{j(i)t} is the year-tt monthly premium bid for beneficiary ii‘s incumbent plan and Benchmarkr(i)tBenchmark_{r(i)t} is the regional benchmark premium in year tt; XitX_{it} includes individual controls. Standard errors are clustered at incumbent-plan-by-year level; bandwidth is restricted to within $6 of the cutoff; region-year fixed effects are included. The design is validated by density tests (Figure 2, p. 2731) and covariate balance checks (Figure 3, p. 2732; Table A1).

Stacked difference-in-differences for drug consumption (Section IV, pp. 2736-2740). To estimate drug consumption effects, the paper stacks all market-year pairs where some plans lose benchmark status, creating a series of experiment-specific difference-in-differences comparisons. The pooled estimating equation (equation 1, p. 2736) is:

yitd=β (BenchmarkLossid×Posttd)+γid+ηtd+ϵitd(1)y_{itd} = \beta\,(\text{BenchmarkLoss}_{id} \times \text{Post}_{td}) + \gamma_{id} + \eta_{td} + \epsilon_{itd} \tag{1}

where yitdy_{itd} is log total allowed prescription drug spending for beneficiary ii in quarter tt in experiment-cohort dd, γid\gamma_{id} are individual-by-experiment fixed effects, and ηtd\eta_{td} are event-time-by-experiment fixed effects. Standard errors clustered at the beneficiary level. Final stacked DiD sample: 5,574,684 person-by-experiment-quarter observations.

Plan-exit experiment (Section VII, pp. 2752-2754). When a plan exits, all enrolled beneficiaries face default reassignment, including prior active choosers. The paper uses the sequence of initial enrollment and post-exit enrollment choices to compare prior passive and active choosers and estimate the share of “sometimes choosers”; it then fits the latent-attention model described below.

RD enrollment effects (R1-R2). Linear probability model on 460,729 beneficiary-year observations from the RD analysis sample. Dependent variable = switched plans (December of year t−1t-1 to January of year tt). Running variable: incumbent plan bid minus regional subsidy. Bandwidth: within $6 of year-tt benchmark; “de minimis” plans (bid above cutoff but below cutoff plus $2) excluded. Results decomposed by outcome type: overall switching, active-choice switching, benchmark-plan active switching, and passive-reassignment switching (columns 1-4 of Table 2, p. 2734).

DiD drug consumption (R3-R4). Stacked DiD per equation (1), outcome = log drug spending. Panel A of Table 3 (pooled across all reassigned beneficiaries): β^=−0.064\hat{\beta} = -0.064 (SE 0.004). Panel B of Table 3 (interacted with worst-quintile fit indicator): main effect β^=−0.043\hat{\beta} = -0.043 (SE 0.004), worst-quintile interaction δ^=−0.083\hat{\delta} = -0.083 (SE 0.007), implying total loss of -12.6% for worst-fitting plans vs -4.3% for others. Effects robust to drug-level price normalization (-5.0%, column 2) and class-level normalization (-2.1%, column 3). Drug-type heterogeneity: high-value drugs -6.2%, chronic drugs -7.8%, non-chronic -2.8% (Table 4, p. 2740). Online Appendix C shows effects persist 24 months.

Active choice elasticity (R5). Same stacked DiD as equation (1) augmented per equation (3) (p. 2745) to identify ∂a/∂vd\partial a / \partial v^d:

yitd=δt(LowestFitid×BenchmarkLossid)+βt BenchmarkLossid+γid+ηtd+ϵitd(3)y_{itd} = \delta_t(\text{LowestFit}_{id} \times \text{BenchmarkLoss}_{id}) + \beta_t\,\text{BenchmarkLoss}_{id} + \gamma_{id} + \eta_{td} + \epsilon_{itd} \tag{3}

where LowestFitid\text{LowestFit}_{id} indicates that the beneficiary’s randomly assigned default plan falls in the bottom quintile of formulary fit for her drug consumption. Identification comes from random assignment of plans to beneficiaries. Outcome = binary active-choice indicator by December. Main effect: β^=0.047\hat{\beta} = 0.047 (SE 0.001). Worst-quintile differential: δ^=0.015\hat{\delta} = 0.015 (SE 0.002) - a 1.5 pp increase in active choice despite a -8.3 pp additional consumption loss. Slope of active choice vs consumption loss is nearly flat across the full range (Figure 7, p. 2749).

Structural attention decomposition (R7). Maximum likelihood estimation of the bivariate normal model Ait=ci+kitA_{it} = c_i + k_{it} on the exiting-plans subsample (32,852 beneficiaries from 84 exiting plans, 28.3% of whom had previously made an active enrollment choice). Variance shares bootstrap-estimated with 1,000 draws. Without covariates: permanent heterogeneity 33.4% [31.4%, 35.4%]; transitory 66.6% [64.6%, 68.6%]. With age/gender/race/health covariates: observable permanent variation = 3.2% [2.9%, 3.8%]; unobservable permanent = 30.6%; transitory = 66.2%. These shares rule out frictional models with constant, stable individual frictions, as they predict the permanent component should dominate.

DatasetRole in paperWiki page
CMS Medicare Beneficiary Summary File (2007-2015)Beneficiary demographics, plan enrollment by month, LIS and Medicare Advantage eligibilityno page yet
CMS Medicaid Personal Summary File (NY and TX, 2004-2010)Demographics and Medicaid eligibility pre-Medicare enrollment for the NY/TX Medicaid-Medicare linked subsampleno page yet
CMS Part D Event Files (2007-2015), 20% samplePrescription drug claims: NDC code, quantity, days supply, date, cost charged to beneficiary and Medicareno page yet
CMS MAX RX Files (NY and TX, 2004-2010), 20% sampleMedicaid prescription claims pre-Medicare enrollment, used to measure prior drug use and plan fitno page yet
CMS Plan Election Type File (2007-2015)Tracks whether each enrollment spell began through active choice or default auto-assignment; also records the assigned default plan even when the beneficiary opted outno page yet
CMS Plan Characteristics Data (publicly available)Plan-level monthly premiums, benchmark status, and formulary coverage by year and service regionno page yet

Sample overview: CMS administrative data for dual-eligible LIS beneficiaries over 65 enrolled in Medicare Parts A, B, and D. Broad LIS sample: 4,628,704 beneficiary-year observations. National MCR initial enrollment sample: 216,772. NY/TX Medicaid-Medicare linked sample: 14,218. RD analysis sample: 1,989,603 (from Table 1, p. 2726); 460,729 beneficiary-year observations restricted to within $6 of the subsidy cutoff. Stacked DiD: 5,574,684 person-by-experiment-quarter observations.

Read the original if you are: (i) evaluating the welfare economics of default design in health insurance and need the full derivation of the optimal default conditions in Online Appendix D; (ii) replicating the RD or stacked DiD designs for other Part D populations or subgroups; (iii) extending the structural attention decomposition to new settings; (iv) studying the institutional details of LIS premium-benchmark rules to design a natural experiment; or (v) modeling attention as a mixture of permanent frictions and transitory shocks in other contexts. The full paper includes Online Appendix E (MLE procedure), Online Appendix C (24-month persistence), and additional robustness tests for the DiD price normalizations and alternative fit measures not covered by this distillation.

Source: peer-reviewed, American Economic Review 113(10), October 2023, pages 2718-2758. DOI: 10.1257/aer.20210013. Replication data and code: ICPSR E184423V1. This distillation was extracted by an LLM on 2026-06-25 and is not human-verified or independently reproduced. The article is paywalled; redistribution is extract-only.

Brot-Goldberg, Zarek, Timothy Layton, Boris Vabson, and Adelina Yanyue Wang. “The Behavioral Foundations of Default Effects: Theory and Evidence from Medicare Part D.” American Economic Review 113, no. 10 (October 2023): 2718-2758. DOI: 10.1257/aer.20210013.

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