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METHODS article

Front. Psychol., 24 April 2018
Sec. Quantitative Psychology and Measurement

Hypothesis-Testing Demands Trustworthy Data—A Simulation Approach to Inferential Statistics Advocating the Research Program Strategy

  • 1Geneva School of Economics and Management, University of Geneva, Geneva, Switzerland
  • 2Institute for Psychology, University of Hamburg, Hamburg, Germany
  • 3Department of Philosophy, Lund University, Lund, Sweden

In psychology as elsewhere, the main statistical inference strategy to establish empirical effects is null-hypothesis significance testing (NHST). The recent failure to replicate allegedly well-established NHST-results, however, implies that such results lack sufficient statistical power, and thus feature unacceptably high error-rates. Using data-simulation to estimate the error-rates of NHST-results, we advocate the research program strategy (RPS) as a superior methodology. RPS integrates Frequentist with Bayesian inference elements, and leads from a preliminary discovery against a (random) H0-hypothesis to a statistical H1-verification. Not only do RPS-results feature significantly lower error-rates than NHST-results, RPS also addresses key-deficits of a “pure” Frequentist and a standard Bayesian approach. In particular, RPS aggregates underpowered results safely. RPS therefore provides a tool to regain the trust the discipline had lost during the ongoing replicability-crisis.


Like all sciences, psychology seeks to establish stable empirical hypotheses, and only “methodologically well-hardened” data provide such stability (Lakatos, 1978). In analogy, data we cannot replicate are “soft.” Recent attempts to replicate allegedly well-established results of null-hypothesis significance testing (NHST), however, did broadly fail. As did the five preregistered replications, conducted between 2014 and 2016, reported in Perspectives of Psychological Science (Alogna et al., 2014; Cheung et al., 2016; Eerland et al., 2016; Hagger et al., 2016; Wagenmakers et al., 2016). This implies that the error-proportions of NHST-results generally are too large. For many more replication attempts should otherwise have succeeded.

We can partially explain the replication failure of NHST-results by citing questionable research practices that inflate the Type-I error probability (false positives), as signaled by a large α-error (Nelson et al., 2018). If researchers collect undersized samples, moreover, then this raises the Type-II error probability (false negatives), as signaled by a large β-error. (The latter implies a lack of sufficient test-power i.e., 1 – β-error). Ceteris paribus, as these errors increase, the replication-probability of a true hypothesis decreases, thus lowering the chance that a replication attempt obtains a similar data-pattern as the original study. Since NHST remains the statistical inference strategy in empirical psychology, many today (rightly) view the field as undergoing a replicability-crisis (Erdfelder and Ulrich, 2018).

It adds severity that this crisis extends beyond psychology—to medicine and health care (Ioannidis, 2014, 2016), genetics (Alfaro and Holder, 2006), sociology (Freese and Peterson, 2017), and political science (Clinton, 2012), among other fields (Fanelli, 2009)—and affects each field as a whole. A 50% replication-rate in cognitive psychology vs. a 25% replication-rate in social psychology (Open Science Collaboration, 2015), for instance, merely makes the first subarea appear more crisis-struck. Since all this keeps from having too much trust in our published empirical results, the term “confidence-crisis” is rather apt (Baker, 2015; Etz and Vandekerckhove, 2016).

The details of how researchers standardly employ NHST coming under doubt has sparked renewed interest in statistical inference. Indeed, many researchers today self-identify as either Frequentists or Bayesians, and align with a “school” (Fisher, Neyman-Pearson, Jeffreys, or Wald). However, statistical inference as a whole offers no more (nor less) than a probabilistic logic to estimate the support that a hypothesis, H, receives from data, D (Fisher, 1956; Hacking, 1965; Edwards, 1972; Stigler, 1986). This estimate is technically an inverse probability, known as the likelihood, L(H|D), and (rightly) remains central to Bayesians.

An important precondition for calculating L(H|D) is the probability of D given H, p(D,H). Unlike L(H|D), we cannot determine p(D,H) other than by induction over data. This (rightly) makes p(D,H) central to Frequentists. Testing H against D—in the sense of estimating L(H|D)—thus presupposes induction, but nevertheless remains distinct conceptually. Indeed, the term “test” in “NHST” misleads. For NHST tests only p(D,H), but not L(H|D). This may explain why publications regularly over-report an NHST-result as supporting a hypothesis. Indeed, many researchers appear to misinterpret NHST as the statistical hypothesis-testing method it emphatically is not.

To clarify why testing p(D,H) conceptually differs from testing L(H|D), this article compares NHST with the research program strategy (RPS), a hybrid-approach that integrates Frequentist with Bayesian statistical inference elements (Witte and Zenker, 2016a,b, 2017a,b). As “stand-ins” for real empirical data, we here simulate the distribution of a (dependent) variable in hypothetical treatment- and control-groups to simulate that variable's arithmetic mean in both groups. Our simulated data are sufficiently similar to data that actual studies would collect for purposes of assessing whether an independent, categorical variable (e.g., an experimental manipulation) significantly influences a dependent variable. Therefore, simulating the parameter-range over which hypothetical data are sufficiently replicable does estimate whether actual data are stable, and hence trustworthy.

We outline RPS [section The Research Program Strategy (RPS)], detail three statistical measures (section Three Measures), explain purpose, method, and the key-result of our simulations (section Simulations), offer a critical discussion (section Discussion), then compare RPS to a “pure” Frequentist and a standard Bayesian approach (section Frequentism Vs. Bayesianism Vs. RPS), and finally conclude (section Conclusion). As supplementary material, we include the R-code, a technical appendix, and an online-app to verify quickly that a dataset is sufficiently stable1.

The Research Program Strategy (RPS)

With the construction of empirical theories as its main aim, RPS distinguishes the discovery context from the justification context (Reichenbach, 1938). The discovery context readily lets us induce a data-subsuming hypothesis without requiring reference to a theoretical construct. Rather, discerning a non-random data-pattern, as per p(D,H0) < α ≤ 0.05, here sufficiently warrants accepting the H1-hypothesis that is a best fit to D as a data-abbreviation. Focusing on non-random effects alone, then, discovery context research is fully data-driven.

In the justification context, by contrast, data shall firmly test a theoretical H1-hypothesis, i.e., verify or falsify the H1 probabilistically. A hypothesis-test must therefore pitch a theoretical H1-hypothesis either against the (random) H0-hypothesis, or against some substantial hypothesis besides the H1 (i.e., H2, …, Hn−1, Hn). Were the H1-hypothesis we are testing indistinct from the data-abbreviating H1, however, then data once employed to induce the H1 now would confirm it, too. As this would level the distinction between theoretical and inductive hypotheses, it made “hypothesis-testing” an empty term. Hence, justification context research must postulate a theoretical H1.

Having described and applied RPS elsewhere (Witte and Zenker, 2016a,b, 2017a,b), we here merely list the six (individually necessary and jointly sufficient) RPS-steps to a probabilistic hypothesis-verification2.

Preliminary discovery

The first step discriminates a random fluctuation (H0) from a systematic empirical observation (H1), measured either by the p-value (Fisher) or the α-error (Neyman-Pearson). Under accepted errors, we achieve a preliminary H1-discovery if the empirical effect sufficiently deviates from a random event.

Substantial discovery

Neyman-Pearson test-theory (NPTT) states the probability that a preliminary discovery is replicable as the (1–β-error), aka test-power. If we replicate a preliminary discovery while α- and β-error (hereafter: α, β) remain sufficiently small, a preliminary H1-discovery turns into a substantial H1-discovery.

Preliminary falsification

A substantial H1-discovery may entail that we thereby preliminarily falsify the H0 (or another point-hypothesis). As the falsification criterion, we propose that the likelihood-ratio of the theoretical effect-size d > 0, postulated by the H1, and of a null-effect d = 0, postulated by the H0, i.e., L(d>0|D)L(d=0|D), must exceed Wald's criterion (1-β)α (Wald, 1943).

Substantial falsification

A preliminary H0-falsification turns into a substantial H0-falsification if the likelihood-ratio of all theoretical effect-sizes that exceed the minimum theoretical effect-size d > δ = dH1dH0, and of the H0(d=0), i.e., L(d>δ|D)L(d=0|D), exceeds the same criterion, i.e., (1-β)α.

Preliminary verification

We achieve a preliminary H1-verification if the likelihood ratio of the point-valued H1(d = δ) and the H0(d=0) exceeds, again, (1-β)α.

Substantial verification

Having preliminarily verified the H1(d=δ) against the H0(d=0), we now test how similar δ is to the empirical (“observed”) effect-size's maximum-likelihood-estimate, MLE(demp). As our verification criterion, we propose the ratio of both likelihood-values (i.e., the maximal ordinate of the normal distribution divided by its ordinate at the 95% interval-point), which is approximately 4 (see next section). If δ's likelihood falls within the 95%-interval centered on MLE(demp), then we achieve a substantial H1-verification. This means we now accept “H1(d=δ)” as shorthand for the effect-size our data corroborate statistically.

RPS thus starts in the discovery context by using p-values (Fisher), proceeds to an optimal3 test of a non-zero effect-size against either a random-model or an alternative model (Neyman-Pearson), and reaches—entering into the justification context—a statistical verification of a theoretically specified effect-size based on probably replicable data4 (see Figure 1). All along, of course, we must assume accepted α- and β-error.


Figure 1. The six steps of the research program strategy (RPS).

In what we call the data space, RPS-steps 1 and 2 thus evaluate probabilities; RPS-steps 3–5 evaluate likelihoods in the hypotheses space; and RPS-step 6 returns to the data space. For data alone determine if the point-hypothesis from RPS-step 5 is substantially verified at RPS-step 6, or not. As if in a circle, then, RPS balances threes steps in the data space (1, 2, 6) with three steps in the hypotheses space (3, 4, 5).

Importantly, individual research groups rarely command sufficient resources to collect a sufficiently large sample that achieves the desirably low error-rates a well-powered study requires (see note 3). To complete all RPS-steps, therefore, groups must coordinate joint efforts, which requires a method to aggregate underpowered studies safely (We return to this toward the end of our next section).

Since RPS integrates Frequentist with Bayesian statistical inference-elements, the untrained eye might discern an arbitrary “hodgepodge” of methods. Of course, the Frequentist and Bayesian schools both harbor advantages and disadvantages (Witte, 1994; Witte and Kaufman, 1997; Witte and Zenker, 2017b). For instance, Bayesian statistics allows us to infer hypotheses from data, but normally demands greater effort than using Frequentist methods. The simplicity and ubiquity of Frequentist methods, by contrast, facilitates the application and communication of research results. But it also risks to neglect assumptions that affect the research process, or to falsely interpret such statistical magnitudes as confidence intervals or p-values (Nelson et al., 2018). Decisively, however, narrowly sticking to any one school would simply avoid attempting to integrate each school's best statistical inference-elements into an all-things-considered best strategy. RPS does just this.

RPS motivates the selection of these elements by its main goal: to construct informative empirical theories featuring precise parameters and hypotheses. As RPS-step 1 exhausts the utility of α, or the p-value (preliminary discovery), for instance, β additionally serves at RPS-step 2 (substantial discovery). In general, RPS deploys inference elements at any subsequent step (e.g., the effect size at RPS-step 2–5; confidence intervals at RPS-step 6) to sequentially increase the information of a preceding step's focal result.

Unlike what RPS may suggest, of course, the actual research process is not linear. Researchers instead stipulate both the hypothesis-content and the theoretical effect-size freely. Nevertheless, a hypothesis-test deserving its name—one estimating L(H|D), that is—requires replicable rather than “soft” data, for such data alone can meaningfully induce a stable effect-size.

RPS therefore measures three qualities: induction quality of data, as well as falsification quality and verification quality of hypotheses, to which we now turn.

Three Measures

This section defines three measures and their critical values in RPS. The first measure estimates how well data sustain an induced parameter; the second and third measure estimate how well replicable data undermine and, respectively, support a hypothesis5.

Def. induction quality: Based on NPTT, we measure induction quality as α and β, given a fixed sample size, N, and two point-valued hypotheses, H0 and H1, yielding the effect-size difference dH1dH0 = δ.

The measure presupposes the effect-size difference dH1dH0 = δ, for otherwise we could not determine test-power (1–β).

Since induction quality pertains to the (experimental) conditions under which one collects data, the measure qualifies an empirical setting's sensitivity. Whether a setting is acceptable, or not, rests on convention, of course. RPS generally promotes α = β = 0.05, or even α = β = 0.01, as the right sensitivity (see section Frequentism Vs. Bayesianism Vs. RPS). By contrast, α = 0.05 and β = 0.20 are normal today. Since βα=0.200.05=4, this makes it four times more important to discover an effect than to replicate it—an imbalance that counts toward explaining the replicability-crisis.

A decisive reason to instead equate both errors (α = β) is that this avoids a bias pro detection (α) and contra replicability (1–β). Given acceptable induction quality, a substantial discovery thus arises if the probability of data passes the critical value (1-β)α. Under α = β = 0.05, for instance, we find that (1-β)α=0.950.05=19. Hence, for the H1 to be statistically significantly more probable than the H0, we have it that p(H1, D) = 19 × p(H0, D).

Thus, we evidently can fully determine induction quality prior to data-collection for hypothetical data. Therefore, the measure says nothing about the focal outcome of a hypothesis-test. As we evaluate L(H|D) in the justification context, by contrast, the same measure nevertheless quantifies the trust that actual data deserve or—as the case may be—require.

Def. falsification quality: Based on Wald's theory, we measure falsification quality as the likelihood-ratio of all hypotheses the effect-size of which exceeds either the H0 (preliminary falsification) or δ (substantial falsification), and the point-valued H0, i.e., L(d > 0|D)/L(d = 0|D). Our proposed falsification-threshold (1−β)/α thus depends on induction quality of data.

The falsification quality measure rests on both the H1 and a fixed amount of actual data. It comparatively tests the point-valued H0 against all point-alternative hypotheses that exceed d H1d H0 = δ. For instance, α = β = 0.05 obviously yields the threshold 19 (or log 19 = 2.94); α = β = 0.01 yields 99 (log 99 = 4.59), etc6. Since it is normally unrealistic to set α = β = 0, “falsification” here demands a statistical sense, rather than one grounding in an observation a deterministic law cannot subsume. Thus, a statistical falsification is fallible rather than final.

The same holds for verification:

Def. verification quality: Again based on Wald's theory, we measure verification quality as the likelihood-ratio of a point-valued H1 and a substantially falsified H0. The threshold for a preliminary verification is again (1-β)α (thus, too, depends on induction quality of data). As the threshold for a substantial verification, we propose the value 4.

To explain this value, RPS views a H1-verification as preliminary if the maximum-likelihood-estimate (MLE) of data falls below the ratio of the maximum corroboration, itself determined via a normal curve's maximal ordinate, viz., 0.3989, and the ordinate at the 95%-interval centered on the maximum, viz., 0.10. As our confirmation threshold, this yields ≈4. Hence, a ratio <4 sees the theoretical parameter lie inside the 95%-interval. RPS would thus achieve a substantial verification.

Following Popper (1959), many take hypothesis-verification to be impossible in a deterministic sense. Understood probabilistically, by contrast, even a substantial verification of one point-valued hypothesis against another such hypothesis is error-prone (Zenker, 2017). The non-zero proportion of false negative decisions thus keeps us from verifying even the best-supported hypothesis absolutely. We can therefore achieve at most relative verification.

Assume we have managed to verify a parameter preliminarily. If the MLE now deviates sufficiently from that parameter's original theoretical value, then we must either modify the parameter accordingly, or may otherwise (deservedly) be admonished for ignoring experience. The MLE thus acts as a stopping-rule, signaling when we may (temporarily) accept a theoretical parameter as substantially verified.

The six RPS steps thus obtain a parameter we can trust to the extent that we accept the error probabilities. Unless strong reasons motivate doubt that our data are faithful, indeed, the certainty we invest into this parameter ought to mirror (1–β), i.e., the replication-probability of data closely matching a true hypothesis (Miller and Ulrich, 2016; Erdfelder and Ulrich, 2018).

Before sufficient amounts of probably replicable data arise in praxis, however, we must normally integrate various studies that each fail the above thresholds. RPS's way of integration is to add the log-likelihood-ratios of two point-hypotheses, each of which is “loaded” with the same prior probability, p(H1) = p(H0) = 0.50. Also known as log-likelihood-addition, RPS thus aggregates data of insufficient induction quality by relying on the well-known equation:


We proceed to simulate select values from the full parameter-range of possible RPS-results. These values are diverse enough to extrapolate to implicit values safely. The subsequent sections offer a discussion and then compare RPS to alternative methodologies.



Using R-software, we simulate data for hypothetical treatment- and control-groups, calculate the group-means, and then compare these means with a t-test. While varying both induction quality of data and the effect-size, we simulate the resulting error rates. Since the simulated error-proportions of a t-test approximate the error-probability of data, this determines the parameter-range over which empirical results (such as those that RPS's six steps obtain) are stable, and hence trustworthy.

In particular, we estimate:

(i) the necessary sample size, NMIN, in order to register, under (1–β), the effect-size δ as a statistically significant deviation from random7;

(ii) the p-value, as the most commonly used indicator in NHST;

(iii) the likelihood that the empirical effect-size d(emp) exceeds the postulated effect-size δ, i.e., L(d > δ|D), as a measure of substantial falsification;

(iv) the likelihood of the H0, i.e., L(δ = 0|D), as a measure of type I and type II errors;

(v) the likelihood of the H1, i.e., the true effect-size L(δ|D), as a measure of preliminary verification;

(vi) the maximum-likelihood-estimate of data, MLE(x), when compared to the likelihood of the H1, as a measure of substantial verification.

We conduct five simulations. Simulations 1 and 2 estimate the probability of true positive and false negative results as a function of the effect-size and test-power. Our significance level is set to α = 0.05, respectively to α = 0.01. Simulation 3 estimates the probability of false positive results. The remaining two simulations address engaging with data in post-hoc fashion. Simulation 4 evaluates shedding 10% of data that least support the focal hypothesis. To address research groups' individual inability to collect the large samples that RPS demands, Simulation 5 mimics collaborative research by adding the log-likelihood-ratios of underpowered studies.

Simulation 1


Simulation 1 manipulates the test-power and the true effect-size to estimate the false negative error-rates (respectively the true positive rate) throughout RPS's six steps.


We manipulate 16 datasets that each contain 100 samples of identical size and variance. We represent a sample by the mean of a normally distributed variable in two independent groups (treatment and control), summarized with the test-statistic t. Between these 16 datasets, we vary the effect-size δ = [0.01, 0.2, 0.5, 0.8], and thus vary the difference between the group-means. We also vary test-power (1–β) = [0.4, 0.5, 0.8, 0.95], and thus let induction quality range from “very poor,” i.e., (1–β) = 0.4, to “medium,” i.e., (1–β) = 0.95. Under α = 0.05 (one-sided), we estimate NMIN to meet the respective test-power (Simulation 2 tightens the significance level to α = 0.01).

Results and Discussion

For both the experimental and the control group, Table 1 lists NMIN to register the effect-size δ as a statistically significant deviation from random (substantial discovery). Generally, given constant test-power (1–β), the smaller (respectively larger) δ is, the larger (smaller) is NMIN. This shows how NMIN depends on β.


Table 1. The estimated minimum sample size for a two sample t-test as a function of test-power (1–β) and effect size δ, given α = 0.05.

For the sample sizes in Table 1, moreover, Table 2 states the proportion of p-values that fall below α = 0.05, given a test-power value. This estimates the probability of a substantial discovery. As the standard deviation of the p-value here indicates, we retain a large variance across samples especially for data of low induction quality.


Table 2. The proportion P of substantial discoveries, indicated by p-values below the significance level α = 0.05, as a function of the effect-size δ and test-power (1–β).


Table 3. The proportion of substantial falsifications and preliminary verifications, as indicated by the respective likelihood ratio (LR) meeting or exceeding the threshold LR(1-β)α.

As with Table 1, Table 2 shows that the larger the test-power value is, the larger is the proportion of substantial discoveries, ceteris paribus. We obtain a similar result when estimating the probability of a substantial falsification or a preliminary verification, as per the likelihood-ratios L(d>0|D)L(d=0|D) and L(d=δ|D)L(d=0|D) meeting the threshold (1-β)α.

In case of a preliminary verification, however, we obtain a larger proportion of false negative results than in case of a substantial falsification. For in verification we narrowly test a point-valued H0 against a point-valued H1. Whereas in falsification we test a point-valued H0 against an interval H1. Therefore, the verification criterion is “less forgiving” than the falsification criterion.

Using bar plots to illustrate the distribution of likelihood-ratios (LRs) for a preliminary verification, Figure 2 shows that LRs often fall below the threshold (1-β)α. However, if data are only of medium induction quality (α = β = 0.05), we find a large proportion of LRs > 3. We should therefore not immediately reject the H1, if (1-β)α < LR > 3, because LR > 3 indicates some evidence for H1. Instead, we should supply additional data before evaluating the LR. If we increase the sample by 50% of its original size, N/2, for instance, but the LR still falls below the threshold, then we may add yet another N/2, and only then sum the log-LRs. If this too fails to yield a preliminary H1-verification (or a H0-verification), then we may still use this empirical result as a parameter-estimate which future studies might test.


Figure 2. Illustration of true positives. Bar plots indicate the frequencies of likelihood ratios (L(d>δ|D)L(d=0|D) set in light gray, and L(d=δ|D)L(d=0|D) in dark gray) that, respectively, fall above the criterion (1-β)α (two leftmost bars), between this criterion and three (two middle bars), and below three (two rightmost bars), as a function of induction quality of data, provided the H1 is true, under α = 0.05 [itself defined via d and (1–β), the latter here abbreviated as “pow”].

An important caveat is that the likelihood-ratio measures the distance between data and hypothesis only indirectly. Even though the likelihood steadily increases as the mean of data approaches the effect-size that the H1 postulates, we cannot infer this distance from the LR alone, but must study the distribution itself. For otherwise, even if LR(1-β)α, we would risk verifying the H1 although the observed mean of data does not originate with the H1-distribution, but with a distinct distribution featuring a different mean.

Moving beyond RPS-step 5, we can only address this caveat adequately by constraining the data-points that substantially verify the H1 to those lying in an acceptable area of variance around the H1. Table 4 reports the proportion of preliminarily H1-verifying samples that now fail the criterion for a substantial H1-verification, and thus amount to additional false negatives. We can reduce these errors by increasing the sample size, which generally reduces the error-probabilities.


Table 4. The proportion of preliminary verifications as per LR(1-β)α, given the empirical effect-size d lies outside the interval comprising 95% of expected values placed around the H1, where L(d|D)L(d=δ|D)>pdf(P50|d)pdf(P95|d)>4.

To account for the decrease in β after constraining the sample size in PRS-step 5, of course, the value of the threshold (1-β)α now is higher, too. Hence, meeting it becomes more demanding. RPS-step 6 nevertheless increases our certainty that the data-mean originates with the hypothesized H1-distribution, and so increases our certainty in the theoretical parameter.

Table 5 states the proportion of datasets that successfully complete RPS's six steps, i.e., preliminary and substantial discovery (steps 1, 2) as well as preliminary and substantial falsification and verification (steps 3–6). For data of low to medium induction quality, we retain a rather large proportion of false negatives.


Table 5. The proportion of substantial verifications, after substantial discoveries and subsequent preliminary verifications were obtained, given the H0 had been substantially falsified.

Simulation 2


To reduce the proportion of false negatives, as we saw, we must increase induction quality of data. Simulation 2 illustrates this by lowering the error-rates.


Repeating the procedure of Simulation 1, but having tightened the error-rates from α = β = 0.05 to α = β = 0.01, we consequently obtain test-power (1–β) = 0.99. This also tightens the threshold from LR > 19 to LR > 99. We drop the smallest effect-size of Simulation 1 (δ = 0.01), for (1–β) = 0.99, after all, makes NMIN = 432,952 unrealistically large (see note 3). Simulation 2 therefore comprises three datasets (each with 100 samples) and manipulates the effect-size as δ = [0.2, 0.5, 0.8].

Results and Discussion

For these three effect sizes, Table 6 states NMIN under α = β = 0.01. Again, the larger (smaller) the effect is, the smaller (larger) is NMIN. Simulated p-values continue to reflect the test-power value almost perfectly (see Table 7). Further, the proportion of preliminary verifications and substantial falsifications (see Table 8) approaches the proportion of substantial discoveries (see Table 7).


Table 6. Sample size for a t-test as a function of δ, given α = β = 0.01.


Table 7. The proportion of substantial discoveries (indicated by the p-value) as a function of δ, given α = β = 0.01.


Table 8. The proportion of substantial falsifications and preliminary verifications, indicated by the respective LR, as a function of δ under α = β = 0.01.

Under high induction quality of data, also the proportion of false negative verifications now is acceptable. When applying the corroboration criterion for a substantial verification, we thus retain only a very small number of additional false negative verifications (see Table 9).


Table 9. The proportion of preliminary verifications as per LR(1-β)α, where the empirical effect size d, however, lies outside the area spanned by the 95%-interval of expected values centered on the H1, and where L(d|D)L(d=δ|D)>pdf(P50|d)pdf(P95|d)>4.

Table 10 reports the proportion of simulated datasets that successfully complete RPS-steps 3–6 in the justification context (preliminary H0-falsification to substantial H1-verification). As before, increasing induction quality of data decreases the proportion of false negative results.


Table 10. The proportion of substantial verifications (subsequent to achieving substantial discoveries and preliminary verifications), given that the H0 was substantially falsified under α = β = 0.01.

Simulation 3


We have so far estimated the probability of true positive and false negative results as per the LR and the p-value. To estimate also the probability of false positive results, Simulation 3 assumes hypothetical effect-sizes and sufficiently large samples to accord with simulated test-power values.


Simulating four datasets (100 samples each), Simulation 3 matches the sample-size to the test-power values (1–β) = [0.4, 0.5, 0.8, 0.95] for a hypothetical effect-size δ = 0.2. In all datasets, the simulated true effect-size is δ = 0.

Results and Discussion

Table 11 shows that simulated p-values reflect our predefined significance level α = 0.05. At this level, a substantial falsification leads to a similar proportion of false positive results as a substantial discovery. By contrast, a preliminary verification decreases the proportion of false positive results to almost zero (see Table 12). Applying the substantial verification-criterion even further decreases the probability of false positive results (see Figure 3).


Table 11. The proportion of false positives, where the sample size, N, is obtained by a priori power analysis, given δ = 0.2 and where (1–β) = [0.4, 0.5, 0.8, 0.95].


Table 12. The proportion of false substantial falsifications and false preliminary verifications using LR(1-β)α.


Figure 3. Illustration of false positives. Bar plots indicate the frequency of likelihood ratios (L(d>δ|D)L(d=0|D) in light gray and L(d=δ|D)L(d=0|D) in dark gray) repeatedly falling above the criterion (1-β)α, between the criterion and three, and below three, as a function of the sample size, provided the H0 is true.

The preceding simulations suggest that, given the threshold LR(1-β)α, the proportion of false negative results remains too large. One might therefore lower the threshold to 3<LR<(1-β)α, which still indicates some evidence for the H1 (see Figure 2). Whether this new threshold reduces the proportion of false negative results unproblematically directly depends on the proportion of false positives. Compared to the case of falsification, however, we now retain a larger proportion of false positives (see Table 13 and Figure 3).


Table 13. The proportion of false preliminary verifications using LR = 3.

As we combine the threshold LR(1-β)α with the substantial verification-criterion, the previous simulations retained a rather large proportion of false negative results. However, this increase occurs only if data are of low to medium induction quality. If induction quality approaches α = β = 0.01, by contrast, then the proportion of both false positive and false negative results decreases to an acceptable minimum. Hence, we may falsify the H0 and simultaneously verify the H1.

Simulation 4


Simulations 1–3 confirmed a simple relation: increasing induction quality of data decreases the proportion of false positive results. Where an actual experimental manipulation fails to produce its expected result, this relation may now tempt researchers to post-hoc manipulate induction quality of data, by shedding some of the “failing” data-points. Simulation 4 investigates the consequences of this move.


Using the samples from Simulation 4, we remove from each sample the 10% of data that score lowest on the dependent variable, thus least support the H1, and then re-assess the proportion of false positive findings.

Results and Discussion

Rather than increase induction quality of data, this post-hoc manipulation produces the opposite result: it raises the proportion of false positive results. On all of our criteria, indeed, shedding the 10% of data that least support the focal hypothesis increases the error-rates profoundly (see Table 14).


Table 14. The proportion of false substantial falsifications and false preliminary verifications, given one had obtained a preliminary discovery (as per the p-value and LR), after 10% of least hypothesis supporting data were removed.

Published data, of course, do not reveal whether someone shed parts of them. Where this manipulation occurs but one cannot trace it reliably, this risks that others draw invalid inferences. For this reason alone, sound inferences should rely on the aggregate results of independent studies (This assumes that data shedding is not ubiquitous). As RPS's favored aggregation method, we therefore simulate a log-likelihood-addition of such results.

Simulation 5


We generally advocate high induction quality of data. Collecting the sizable NMIN (that particularly laboratory studies require) to meet test-power = 0.99 (or merely 0.95), however, can quickly exhaust an individual research group's resources (see Lakens et al., 2018)8. In fact, we often have no other choice but to aggregate comparatively “soft” (underpowered) data from multiple studies. Aggregate data, of course, must reflect the trust each dataset deserves individually. We therefore simulate the addition of logarithmic LRs (log-LRs) for data of low to medium test-power.


We add the log-LRs as per the low-powered samples of Simulation 1, then assess the proportions of samples that meet the criteria of each RPS-step. Notice that this is the only way to conduct a global hypothesis-test that combines individual studies safely (It is nevertheless distinct from a viable meta-analytic approach; see Birnbaum, 1954).

Results and Discussion

Table 15 shows that the log-LRs of three low-powered studies under (1–β) = [0.4, 0.5, 0.8] aggregate to one medium-powered study under (1–β) = 0.95 (see Table 3), because the three samples sum to NMIN for a substantial discovery under (1–β) = 0.95. The probability of correctly rejecting the H0 thus approaches 1, whereas the proportion of preliminary verifications is not much larger than for each individual study (see Table 3; last row). This means individual research groups can collect fewer data points than NMIN. Thus, log-LR addition indeed optimizes a substantial H0-falsification.


Table 15. The proportions of LR(1-β)α when adding the log(LR) of individually underpowered studies featuring (1–β) = [0.4, 0.5, 0.8].

Simulations 1–5 recommend RPS primarily for its desirably low error-rates, which to achieve made induction quality of data and likelihood-ratios central. Particularly Simulation 5 shows why log-likelihood-ratio addition of individually under-powered studies can meet the rigorous test-power demands of the justification context, viz. (1–β) = 0.95, or better yet (1–β) = 0.99.


As an alternative to testing the H1 against H0 = 0, we may pitch it against H0 = random. Following a reviewer's suggestion, we therefore also simulated testing the mean-difference between the treatment- and the control-group against the randomly varying mean-difference between the control-group and zero. Compared to pitching the H1 against H0 = 0, this yields a reduced proportion of false negatives, but also generates a higher proportion of false positives.

Since our sampling procedure lets the mean-difference between control group and zero vary randomly around zero, the increase in false positives (negatives) arises from the control group's mean-difference falling below (above) zero in roughly 50% of all samples. This must increase the LR in favor of the H1 (H0). With respect to comparing group-means, however, testing the H1 against H0 = random does not prove superior to testing it against H0 = 0, as in RPS.

In view of RPS, if induction quality of data remains low (α = β > 0.05), then we cannot hope to either verify or falsify a hypothesis. This restricts us to two discovery context-activities: making a preliminary or a substantial discovery (RPS-step 1, 2). After all, since both discovery-variants arise from estimating p(D,H), this rules out hypothesis-testing research, which instead estimates L(H|D).

By contrast, achieving medium induction quality (α = β ≤ 0.05) meets a crucial precondition for justification context-research. RPS can now test hypotheses against “hard” data by estimating L(H|D). Specifically, RPS tests a preliminary, respectively a substantial H0-falsification (RPS-steps 3, 4), by testing if L(d>0|D)L(d=0|D), respectively L(d=δ|D)L(d=0|D), exceeds (1-β)α. If the latter holds true, then we can test a preliminary verification of the theoretical effect-size H1-hypothesis (RPS-step 5) as to whether L(d=δ|D)L(d=0|D) exceeds (1-β)α. If so, then we finally test a substantial H1-verification (RPS-step 6)—here using the ratio of the MLE of data and the likelihood of the H1(d=δ)—as to whether δ falls within the 95%-interval centered on the MLE [If not, we may adapt H1(d=δ) accordingly, provided both theoretical and empirical considerations support this].

As we saw, RPS almost eliminates the probability of a false positive H1-verification. If data are of medium induction quality, moreover, then the probability of falsely rejecting the H1 lies in an acceptable range, too (This range is even slightly smaller than that for false positive verifications). However, lowering the threshold (1-β)α to decrease the probability of false negatives will increase the probability of false positives. In balancing false positive with false negative H1-verifications, then, we face an inevitable trade-off.

To increase the probability of false positives is generally more detrimental to a study's global outcome than to decrease the probability of false negatives. After all, since editors and reviewers typically prefer significant results (p < α = 0.05), non-significant results more often fail the review process, or are not written-up (Franco et al., 2014). This risks that the community attends to more potentially false positive than potentially false negative results9. That researchers should reduce this risk thus speaks decisively against lowering the threshold. To control the risk, moreover, it suffices to increase induction quality of data by adding additional samples until N = NMIN.

In psychology as elsewhere today, the standard mode of empirical research clearly differs from what RPS recommends; particularly induction quality (test-power) appears underappreciated. Yet, what besides a substantial H1-verification can provide a statistical warrant to accept a H1 that aptly pre- or retrodicts a phenomenon? Likewise, only a substantial H0-falsification can warrant us in rejecting the H0 (For reasons given earlier, p-values alone will not do).

The discovery context as RPS's origin and the justification context as its end, RPS employs empirical knowledge to gain theoretical knowledge. A theory is generally more informative the more possible states-of-affairs it rules out. The most informative kind of theory, therefore, lets us deduce hypotheses predicting precise (point-specified) empirical effects—effects we can falsify statistically10. Obvious candidates for such point-values are those effects that “hard” data support sufficiently. RPS's use of statistical inference toward constructing improved theories thus reflects that, rather than one's statistical school determining the most appropriate inference-element, this primarily depends on the prior state of empirical knowledge we seek to develop.

Such prior knowledge we typically gain via meta-analyses that aggregate the samples and effect-sizes of topically related object-level studies. These studies either estimate a parameter or test a hypothesis against aggregated data, but typically are individually underpowered. A meta-analysis now tends to join an estimated combined effect-size of several studies, one on hand, with the estimated sum of their confidence intervals deviating from the H0, on the other. This aggregate estimate, however, thus rests on data of variable induction quality. A similar aggregation method, therefore, can facilitate only a parameter-estimation, but it will not estimate L(H|D) safely.

A typical meta-analysis indeed ignores the replication-probability of object-level studies, instead considering only the probability of data, p(D,H)11. This makes it an instance of discovery context-research. By contrast, log-likelihood-addition is per definition based on trustworthy data (of high induction quality), does estimate L(H|D) safely, and hence is an instance of justification context-research (see sections Three Measures and Discussion).

RPS furthermore aligns with the registered replication reports-initiative (RRR), which aims at more realistic empirical effect-size estimates by counteracting p-hacking and publication bias (Bowmeester et al., 2017). Indeed, RPS complements RRR. Witte and Zenker's (2017a) re-analysis of Hagger et al.'s (2016) RRR of the ego-depletion effect, for instance, strengthens the authors' own conclusions, showing that their data lend some 500 times more support to the H0(d=0.00) than to the H1(d=0.20).

Both RRR and RPS obviously advocate effortful research. Though we could coordinate such efforts across several research groups, current efforts are broadly individualistic and tend to go into making preliminary discoveries. This may yield a more complex view upon a phenomenon. Explaining, predicting, and intervening, however, all require theories with substantially verified H1-hypotheses as their deductive consequences. Again, constructing a more precise version of such a theory is RPS's main aim. Indeed, we need something like RPS anyways. For we can statistically test hypotheses by induction [see section The Research Program Strategy (RPS)], but we cannot outsource theory-construction to induction.

Frequentism vs. Bayesianism vs. RPS

A decisive evaluative criterion is whether an inference strategy leads to a rigorously validated, informative theory. Researchers can obviously support this end only if their individual actions relate to what the research community does as a whole. At the same time, each researcher must balance her own interests with those of others. Hence, we exercise “thrift” when collecting small samples, but also publish the underpowered results this generates to further our careers.

Reflecting the research community's need for informative theories, most journals require that a submitted manuscript report at least one statistically significant effect—that is, a preliminary discovery à la NHST (For an exception, see Trafimow, 2014). Given this constraint, the favored strategy to warrant our publication activities seemingly entails conducting “one-shot”-experiments, leading to many papers without integrating their results theoretically.

That strategy's probably best defense offers three supporting reasons: (i) the strategy suffices to discover non-random effects; (ii) non-random effects matter in constructing informative theories; (iii) the more such discoveries the merrier. However, (i) is a necessary (rather than a sufficient) reason that the strategy is apt; (ii) is an insufficient supporting reason, for non-randomness matters but test-power counts (Witte and Zenker, 2018); and (iii) obviously falls with (ii). Therefore, this defense cannot sufficiently support that the strategy balances the interests of all concerned parties. Indeed, the status quo strongly favors the individual's career aspirations over the community's need for informative theories.

The arguably best statistical method to make a discovery remains a Fisher-test (For other methods, see, e.g., Woodward, 1989; Haig, 2005). It estimates the probability of an empirical effect given uncontrollable, but non-negligible influences. This probability meeting a significance-threshold such as p(H,D) < α = 0.05, as we saw, is a necessary and sufficient condition for a preliminary discovery (RPS-step 1). Though this directs our attention to an empirical object, it also exhausts what NHST by itself can deliver. Subsequent RPS-steps therefore employ additional induction quality measures, namely the effect-size (steps 2–5) and offer a new way of using confidence intervals (step 6).

Recent critiques of NHST give particular prominence to Bayesian statistics. As an alternative to a classical t-test, for instance, many promote a Bayesian t-test. This states the probability-ratio of data given a hypotheses-pair, p(D|H1)/p(D|H0), a ratio that is known as the “Bayes factor” (Rouder et al., 2009; Wetzels et al., 2011). If the prior probabilities are identical, p(H1) = p(H0) = 0.50, then the Bayes factor is the likelihood-ratio of two point-hypotheses, L(H1|D)/L(H0|D). Indeed, RPS largely is coextensive with a Bayesian approach as concerns the hypothesis space.

But Bayesians must also operate in the data space, particularly when selecting data-distributions as priors for an unspecified H1. Such substantial assumptions obviously demand a warrant. For the systematic connection between the Bayes-factor and the p-value of a classical t-test is that “default Bayes factors and p-values largely covary with each other” (Wetzels et al., 2011, 295). The main difference is their calibration: “p-values accord more evidence against the null [hypothesis] than do Bayes factors” (ibid).

The keyword here is “default.” For the default prior probabilities one assumes matter when testing hypotheses. In fact, not only do Bayesians tend to assign different default priors to the focal H0 and the H1; they also tend to distribute (rather than point-specify) these priors. As Rouder et al. (2009, 229) submit, for instance, “[…] we assumed that the alternative [hypothesis] was at a single point”—an assumption, however, which allegedly is “too restrictive to be practical” (ibid). Rather, it be “more realistic to consider an alternative [hypothesis] that is a distribution across a range of outcomes” (ibid), although “arbitrarily diffuse priors are not appropriate for hypothesis testing” (p. 230) either. This can easily suggest that modeling a focal parameter's prior probability distributively would be the innocent choice it is not.

After all, computing a Bayesian t-test necessarily incurs not only a specific prior data-distribution, but also a point-specified scaling factor. This factor is given by the prior distributions of the focal hypotheses, i.e., as the ratio p(H1)/p(H0) [see our formula (1), section Three Measures]. Prior to collecting empirical data, therefore, p(H1)/p(H0) < 1 reflects a (subjective) bias pro the H0–which lets data raise the ratio's denominator—while p(H1)/p(H0) > 1 reflects a preference contra the H0.

If the priors on the H0 and the H1 are unbiased, by contrast, then the scaling factor “drops out.” It thus qualifies as a hidden parameter. Alas, unbiased priors are the exception in Bayesian statistics. A default Bayesian t-test, for instance, normally assumes both a Cauchy distribution and a scaling factor of 0.707. Both assumptions are of the same strength as the assumptions that RPS incurs to point-specify the H1. The crucial difference, however, is that the two Bayesian assumptions concern the data space, whereas RPS's assumptions pertain to the hypotheses space.

Unlike RPS's assumptions, the two Bayesian assumptions thus substantially influence the shape of possible data. For the scaling factor's value grounds in the type of the chosen prior-distribution, which hence lets the Bayes factor vary noticeably. Different default priors can thus lead to profound differences as to whether data corroborate the H0- or the H1-hypothesis

Moreover, a Bayesian t-test's result continues to depend on the sample size, and lacks information on the replication-probability of data given a true hypothesis.

The most decisive reason against considering a standard Bayesian approach an all-things-considered best inference strategy, finally, is that it remains unclear how to sufficiently justify this or that scaling factor, or distribution, not only “prior to analysis[, but also] without influence from [sic] data” (Rouder et al., 2009, 233; italics added). Indeed, the need to fix a Bayesian t-test's prior-distribution alone already fully shifts the decision—as to the elements an inference strategy should (not) specify—from the hypotheses space to the data space. This injects into the debate a form of subjectivity that point-specifying the H1 would instead make superfluous.

One should therefore treat a Bayesian t-test with utmost caution. For rather than render hypothesis testing simple and transparent, a Bayesian t-test demands additional efforts to bring its hidden parameters and default priors back into view. We would hence do well to separate our data exploration-strategy clearly from our hypothesis-testing machinery. The Bayesian approach, however, either would continue not to mark a clear boundary or soon look similar to RPS's hybrid-approach12.

To summarize the advantages RPS offers over both a pure Frequentist and a standard Bayesian approach:

(i) RPS uses NPTT to determine the minimum sample size, NMIN, that suffices to conduct research under at least medium induction quality of data (α = β < 0.05);

(ii) the RPS hypothesis corroboration-threshold is sensitive to both errors (α, β);

(iii) to facilitate an aggregate hypothesis-evaluation (balancing resource restrictions with career aspirations), RPS uses log-likelihood-addition to integrate individually underpowered studies.

RPS thus makes explicit why a statistical result depends on the sample-size, N. Using a point-alternative hypothesis particularly shows that the Bayes-factor varies with N, which otherwise remains “hidden” information. Throughout RPS's six steps, the desirably transparent parameter to guide the acceptance or rejection of a hypothesis (as per Wald's criterion) is induction quality of data (test-power).

Finally, notice that the “new statistics” of Cumming (2013) only pertains to the data space. As does Benjamin et al.'s (2018) proposal to lower α drastically. For it narrowly concerns a preliminary discovery (RPS-step 1), but leaves hypothesis-testing unaddressed (also see Lakens et al., 2018). To our knowledge, no equally appropriate and comprehensive strategy currently matches the inferential capabilities that RPS offers (Wasserstein and Lazar, 2016).


RPS is a hybrid-statistical approach using tools from several statistical schools. Its six hierarchical steps lead from a preliminary H1-discovery to a substantial H1-verification. Each step not only makes a prior empirical result from an earlier step more precise, our simulations also show that completing RPS's six steps nearly eliminates the probability of false positive H1-verifications. If data are of medium induction quality, moreover, then also the probability of falsely rejecting the H1 lies in an acceptable range.

Having simulated a broad range of focal parameters (α, β, d, N), we may extrapolate to implicit ranges safely. This lets us infer the probable error-rates of studies that were conducted independently RPS and thus allows estimating how trustworthy a given such result is. The online-tool we supply indeed makes this easy.

We advocate RPS primarily for the very low error-rates of its empirical results (Those feeling uncertain about such RPS-results may further increase the sample, to obtain yet lower error-rates). Moreover, an integration of individually underpowered studies via log-likelihood-addition not only is meaningful, it can also meet the test-power demands of the justification context. Therefore, research groups may cooperate such that each group collects fewer that the minimum number of data points.

Null-hypothesis significance testing by itself can at most deliver a preliminary discovery (RPS-step 1). This may motivate new research questions, which for RPS is merely an intermediate goal; the aim is to facilitate theory development and testing. Since most current research in psychology as elsewhere stops at RPS-step 1, however, this cannot suffice to construct well-supported and informative theories. Indeed, that an accumulation of preliminary discoveries could lead to a well-supported theory ever remains a deeply flawed idea.

Author Contributions

The idea for RPS originates with EW. FZ and EW jointly developed its presentation. AK-S programed and ran the simulations. EW wrote the first draft of the manuscript; all authors edited it and approved the final version.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.


We thank Paul T. Barrett and Aristides Moustakas for constructive comments that helped improve an earlier version of this manuscript. We also thank Holmes Finch for overseeing the review process. AK-S acknowledges a research grant from the Swiss National Science Foundation, and open access funding from the University of Geneva. FZ acknowledges funding from the Ragnar Söderberg Foundation, the Volkswagen Foundation, the HANBAN institute, and a European Union MSC-COFUND fellowship, as well as open access funding from Lund University.


1. ^See for the R-code; find the online-tool at

2. ^Our focus here is on the quantitative evaluation of hypotheses by empirical data. The current presentation of RPS therefore both excludes qualitative research processes preceding data-collection like conjecturing phenomena or constructing experimental designs (see Flick, 2014) as well as subsequent processes like embedding data into an informative theory. Both process kinds employ observation and interpretation, but also rely on scholarly argument referencing more than statistical data alone. Nonetheless, insofar as empirical data are independent of a researcher's prior belief, such data are necessary to run a research program.

3. ^The smallest sample, NMIN, sufficing in NPTT to identify a point-specified effect as a statistically significant deviation from random, is a function of α, β, and d. Under conventional errors (e.g., α = β ≤ 0.05), therefore, given any sample, N, a significance-test is optimal if N = NMIN. With both hypothesis-verification and -falsification alike, however, if N > NMIN, then the utility of additional data decreases. Under α = 0.05 (one-tailed), for instance, already N = 500 let the very small effect d = 0.10 become statistically significant, even though it “explains” but 0.002% of data-variance. Once N > 60.000, this utility vanishes. Almost any way of partitioning a very large sample now makes virtually the smallest effect statistically significant (Bakan, 1966).

This may seem paradoxical because the law of great numbers states that, ceteris paribus, enlarging N increases the validity of a parameter-estimate. At N > 60,000, however, measuring virtually any variable “reveals” that it significantly deviates from some predicted value. In a statistical sense, all unknown influences can now sufficiently manifest themselves, which lets any parameter-value become equally admissible. But if every parameter could become statistically significant, then none would be particularly important. Ad absurdum, then, as concerns hypothesis-testing the claim “more data is always better” is false in the hypotheses space. It nevertheless holds that increasing the sample yields an ever more precise parameter-estimate in the data space.

4. ^Fixing the H0-parameter as d = 0, as a random-model has it, is merely a convention, of course. In fact RPS can alternatively base the H0-parameter on a control-group (as is typical), or on a simpler model (that eliminates elements of a more complex model), or on a rivaling theoretical model. In any case, not to remain ignorant of α, β, N, d, we must specify the H0.

5. ^Witte and Zenker (2017b) presented the second and third measure as if they were one.

6. ^Using “log” to abbreviate the logarithmus naturalis (ln), as per the command in R, in previous work we used “log” to abbreviate the logarithmus decimalis (Witte and Zenker, 2017b). Results are independent of nomenclature, of course, except that the critical values then came to 1.28 and 2.00.

7. ^The term “random” is shorthand for a normalized mean, irrespective of whether we assume random influences, work with a control group or a simpler model (featuring fewer parameters), or with a theoretical alternative model.

8. ^Governing the praxis of enlarging the sample until we reach sufficient test-power is the assumption that the focal theoretical parameter is the mean at the group level, whereas participant behavior at the individual level fluctuates randomly. If we instead focus on the potential non-random variation at the individual level, of course, then it is not the size of the sample (number of participants) that counts, but the number of repeated measurements we perform on a single participant. With a “small-N design,” indeed, the population is the single participant (see Smith and Little, 2018). Provided our indicators are valid and reliable, repeated measurements on a single participant may in fact detect idiosyncratic influences that averaging at the group level could distort. But rather than offer an alternative to large sample research, a small-N design serves a distinct purpose, and so complements large sample research.

9. ^Things might look different if, next to a truth-criterion (based on error probabilities), we employ external utilities, too (Miller and Ulrich, 2016). Even where we can motivate such utilities unproblematically, we must ever compare the empirical proportions of simulated false positive results vs. false negative substantial verifications. Under medium induction quality (α = β = 0.05), the odds-ratio roughly is 1:5, under high induction quality (α = β = 0.01) it is 1:10. To compare with the proportion of substantial discoveries and substantial falsifications, under medium induction quality the odds-ratio decreases to about 1:2; under high induction quality nearly to 1:1. As we saw in the previous section, the asymmetry itself arises from comparing a point-parameter in case of false negatives, with a distributed-parameter (an interval) in case of false positives.

10. ^If we are uncertain which point-hypothesis best specifies a theoretical parameter, then we may generalize the parameter from a point- to an interval-hypothesis. The interval's end-points thus state distinct (hypothetical) effect-sizes; the middle point qualifies as a theoretical assumption. To achieve constant induction quality, of course, we must confront each end-point with its appropriate sample size. To this end, log-likelihood-addition lets us increase the sample associated to the larger effect-size until we reach the appropriate sample-size for the smaller effect-size.

11. ^Here, we can neither discuss meta-analysis as a method, nor adequately address the replication of empirical studies. We show elsewhere how to statistically establish hypotheses by integrated efforts, particularly addressing Bem's psi-hypothesis (Witte and Zenker, 2017b) and the ego-depletion effect (Witte and Zenker, 2017a).

12. ^Schönbrodt and Wagenmakers's (2018) recent Bayes factor design analysis (BFDA), for instance, clearly recognizes the need to first plan an empirical setting, to only then evaluate the degree to which actual data falsify or verify a hypothesis statistically. This same need lets RPS characterize the setting via induction quality of data. While the planning stage is independent of the analysis stage, RPS's Wald-criterion not only provides a bridge between them, it also functions as a threshold with known consequences. Unlike BFDA and similar Bayesian approaches, however, RPS avoids setting subjective priors and relies solely on the likelihood-function.


Alfaro, M. E., and Holder, M. T. (2006). The posterior and the prior in Bayesian phylogenetics. Annu. Rev. Ecol. Evol. Syst. 37, 19–42. doi: 10.1146/annurev.ecolsys.37.091305.110021

CrossRef Full Text | Google Scholar

Alogna, V. K., Attaya, M. K., Aucoin, P., Bahnik, S., Birch, S., Birt, A. R., et al. (2014). Registered replication report: Schooler & Engstler-Schooler. (1990). Perspect. Psychol. Sci. 9, 556–578. doi: 10.1177/1745691614545653

PubMed Abstract | CrossRef Full Text | Google Scholar

Bakan, D. (1966). The test of significance in psychological research. Psychol. Bull. 66, 423–437. doi: 10.1037/h0020412

PubMed Abstract | CrossRef Full Text | Google Scholar

Baker, M. (2015). First results from psychology's largest reproducibility test. Nature. doi: 10.1038/nature.2015.17433

CrossRef Full Text

Benjamin, D. J., Berger, J., Johannesson, M., Nosek, B. A., Wagenmakers, E.-J., Berk, R., et al. (2018). Redefine statistical significance. Nat. Human Behav. 2, 6–10. doi: 10.1038/s41562-017-0189-z

CrossRef Full Text | Google Scholar

Birnbaum, A. (1954). Combining independent tests of significance. J. Am. Statist. Assoc. 49, 559–574.

Google Scholar

Bowmeester, S., Verkoeijen, P. P. J. L., Aczel, B., Barbosa, F., Bègue, L., Brañas-Garza, P., et al. (2017). Registered replication report: Rand, Greene, and Nowak (2012). Perspect. Psychol. Sci. 12, 527–542. doi: 10.1177/1745691617693624

CrossRef Full Text | Google Scholar

Cheung, I., Campbell, L., LeBel, E., and Yong, J. C. (2016). Registered replication report: study 1 from Finkel, Rusbult, Kumashiro, & Hannon (2002). Perspect. Psychol. Sci. 11, 750–764. doi: 10.1177/1745691616664694

PubMed Abstract | CrossRef Full Text | Google Scholar

Clinton, J. D. (2012). Using roll call estimates to test models of politics. Ann. Rev. Pol. Sci. 15, 79–99. doi: 10.1146/annurev-polisci-043010-095836

CrossRef Full Text | Google Scholar

Cumming, G. (2013). The new statistics: why and how. Psychol. Sci. 20, 1–23. doi: 10.1177/0956797613504966

CrossRef Full Text | Google Scholar

Edwards, A. W. F. (1972). Likelihood. Cambridge: Cambridge University Press (expanded edition, 1992, Baltimore: Johns Hopkins University Press).

Google Scholar

Eerland, A., Sherrill, A. M., Magliano, J. P., Zwaan, R. A., Arnal, J. D., Aucoin, P., et al. (2016). Registered replication report: Hart & Albarracín (2011). Perspect. Psychol. Sci. 11, 158–171. doi: 10.1177/1745691615605826

PubMed Abstract | CrossRef Full Text | Google Scholar

Erdfelder, E., and Ulrich, R. (2018). Zur Methodologie von Replikationsstudien [On a methodology of replication studies]. Psychol. Rundsch. 69, 3–21. doi: 10.1026/0033-3042/a000387

CrossRef Full Text | Google Scholar

Etz, A., and Vandekerckhove, J. (2016). A Bayesian perspective on the reproducibility project: psychology. PLoS ONE 11:e0149794. doi: 10.1371/journal.pone.0149794

PubMed Abstract | CrossRef Full Text | Google Scholar

Fanelli, D. (2009). How many scientists fabricate and falsify research? A systematic review and meta-analysis of survey data. PloS ONE 4:e5738. doi: 10.1371/journal.pone.0005738

PubMed Abstract | CrossRef Full Text | Google Scholar

Fisher, R. A. (1956). Statistical Methods and Scientific Inference. New York, NY: Hafner.

Google Scholar

Flick, U. (ed.). (2014). The SAGE Handbook of Qualitative Data Analysis. London: Sage.

Google Scholar

Franco, A., Malhotra, N., and Simonovits, G. (2014). Publication bias in the social sciences: unlocking the file drawer. Science 345, 1502–1505. doi: 10.1126/science.1255484

PubMed Abstract | CrossRef Full Text | Google Scholar

Freese, J., and Peterson, D. (2017). Replication in social science. Annu. Rev. Sociol. 43, 147–165. doi: 10.1146/annurev-soc-060116-053450

CrossRef Full Text | Google Scholar

Hacking, I. (1965). Logic of Statistical Inference. Cambridge: Cambridge University Press.

Google Scholar

Hagger, M. S., Chatzisarantis, N. L. D., Alberts, H., Anggono, C. O., Batailler, C., Birt, A. R., et al. (2016). A multilab preregistered replication of the ego-depletion effect. Perspect. Psychol. Sci. 11, 546–573. doi: 10.1177/1745691616652873

PubMed Abstract | CrossRef Full Text | Google Scholar

Haig, B. (2005). An abductive theory of scientific method. Psychol. Methods 10, 371–388. doi: 10.1037/1082-989X.10.4.371

PubMed Abstract | CrossRef Full Text | Google Scholar

Ioannidis, J. P. A. (2014). How to make more published research true. PLoS Med. 11:e1001747. doi: 10.1371/journal.pmed.1001747

PubMed Abstract | CrossRef Full Text | Google Scholar

Ioannidis, J. P. A. (2016). The mass production of redundant, misleading, and conflicted systematic reviews and meta-analyses. Milbank Q. 94, 485–514. doi: 10.1111/1468-0009.12210

PubMed Abstract | CrossRef Full Text | Google Scholar

Lakatos, I. (1978). The Methodology of Scientific Research Programmes, Vol. I, eds J. Worrall and G. Currie. Cambridge, UK: Cambridge University Press.

Lakens, D., Adolfi, F. G., Albers, C., Anvari, F., Apps, M. A. J., Argamon, S. E., et al. (2018). Justify your alpha. Nat. Hum. Behav. 2, 168–171. doi: 10.1038/s41562-018-0311-x

CrossRef Full Text | Google Scholar

Miller, J., and Ulrich, R. (2016). Optimizing research payoff. Perspect. Psychol. Sci. 11, 661–691. doi: 10.1177/1745691616649170

PubMed Abstract | CrossRef Full Text | Google Scholar

Nelson, L. D., Simmons, J., and Simonsohn, U. (2018). Psychology's Renaissance. Annu. Rev. Psychol. 69, 511–534. doi: 10.1146/annurev-psych-122216-011836

PubMed Abstract | CrossRef Full Text | Google Scholar

Open Science Collaboration (2015). Estimating the reproducibility of psychological science. Science 349:acc4716. doi: 10.1126/science.aac4716

CrossRef Full Text

Popper, K. R. (1959). Logic of Scientific Discovery. London: Basic Books.

Google Scholar

Reichenbach, H. (1938). Experience and Prediction. Chicago, IL: University of Chicago Press.

Google Scholar

Rouder, J. N., Speckman, P. L., Sun, D., Morey, R. D., and Iverson, G. (2009). Baysian t-tests for accepting and rejecting the null hypothesis. Psychon. Bull. Rev. 16, 225–237. doi: 10.3758/PBR.16.2.225

CrossRef Full Text | Google Scholar

Schönbrodt, F., and Wagenmakers, E.-J. (2018). Bayes factor design analysis: planning for compelling evidence. Psychon. Bull. Rev. 25, 128–142. doi: 10.3758/s13423-017-1230-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Smith, P. L., and Little, D. R. (2018). Small is beautiful: In defense of the small-N design. Psychon. Bull. Rev. doi: 10.3758/s13423-018-1451-8. [Epub ahead of print].

PubMed Abstract | CrossRef Full Text | Google Scholar

Stigler, S. (1986). The History of Statistics: The Measurement of Uncertainty before 1900. Cambridge, MA: Harvard University Press.

Google Scholar

Trafimow, D. (2014). Editorial. Basic Appl. Soc. Psychol. 36, 1–2. doi: 10.1080/01973533.2014.865505

CrossRef Full Text

Wagenmakers, E.-J., Beek, T., Dijkhoff, L., Gronau, Q. F., Acosta, A., Adams, R. B., et al. (2016). Registered replication report: Strack, Martin, and Stepper. (1988). Perspect. Psychol. Sci. 11, 917–928. doi: 10.1177/1745691616674458

PubMed Abstract | CrossRef Full Text | Google Scholar

Wald, A. (1943). Tests of statistical hypotheses concerning several parameters when the number of observations is large. Trans. Am. Math. Soc. 54, 426–482. doi: 10.1090/S0002-9947-1943-0012401-3

CrossRef Full Text | Google Scholar

Wasserstein, R. L., and Lazar, N. A. (2016). The ASA's statement on p-values: context, process, and purpose. Am. Stat. 70, 129–133. doi: 10.1080/00031305.2016.1154108

CrossRef Full Text | Google Scholar

Wetzels, R., Matzke, D., Lee, M. D., Rouder, J. N., Iverson, G. J., and Wagenmakers, E.-J. (2011). Statistical evidence in experimental psychology: an empirical comparison using 855 t-tests. Perspect. Psychol. Sci. 6, 291–298. doi: 10.1177/1745691611406923

PubMed Abstract | CrossRef Full Text | Google Scholar

Witte, E. H. (1994). A Statistical Inference Strategy (FOSTIS): A Non-Confounded Hybrid Theory. HAFOS, 9. Available online at: (Accessed August 8, 2016).

Witte, E. H., and Kaufman, J. (1997). The Stepwise Hybrid Statistical Inference Strategy: FOSTIS. HAFOS, 18. Available online at: (Accessed April 6, 2018).

Witte, E. H., and Zenker, F. (2016a). Reconstructing recent work on macro-social stress as a research program. Basic Appl. Soc. Psychol. 38, 301–307. doi: 10.1080/01973533.2016.1207077

CrossRef Full Text | Google Scholar

Witte, E. H., and Zenker, F. (2016b). Beyond schools—reply to Marsman, Ly & Wagenmakers. Basic Appl. Soc. Psychol. 38, 313–317. doi: 10.1080/01973533.2016.1227710

CrossRef Full Text | Google Scholar

Witte, E. H., and Zenker, F. (2017a). Extending a multilab preregistered replication of the ego-depletion effect to a research program. Basic Appl. Soc. Psychol. 39, 74–80. doi: 10.1080/01973533.2016.1269286

CrossRef Full Text | Google Scholar

Witte, E. H., and Zenker, F. (2017b). From discovery to justification. Outline of an ideal research program in empirical psychology. Front. Psychol. 8, 1847. doi: 10.3389/fpsyg.2017.01847

PubMed Abstract | CrossRef Full Text | Google Scholar

Witte, E. H., and Zenker, F. (2018). Data replication matters, replicated hypothesis-corroboration counts. (Commentary on “Making Replication Mainstream” by Rolf A. Zwaan, Alexander Etz, Richard E., Lucas, and M. Brent Donnellan). Behav. Brain Sci. (forthcoming).

Woodward, J. (1989). Data and phenomena. Synthese 79, 393–472. doi: 10.1007/BF00869282

CrossRef Full Text | Google Scholar

Zenker, F. (2017). “Falsification,” in The Wiley Encyclopedia of Social Theory, ed B. Turner (Chichester: Wiley Blackwell), 1–3.

Google Scholar

Keywords: Bayes' theorem, inferential statistics, likelihood, replication, research program strategy, t-test, Wald criterion

Citation: Krefeld-Schwalb A, Witte EH and Zenker F (2018) Hypothesis-Testing Demands Trustworthy Data—A Simulation Approach to Inferential Statistics Advocating the Research Program Strategy. Front. Psychol. 9:460. doi: 10.3389/fpsyg.2018.00460

Received: 18 October 2017; Accepted: 19 March 2018;
Published: 24 April 2018.

Edited by:

Holmes Finch, Ball State University, United States

Reviewed by:

Paul T. Barrett, Advanced Projects R&D Ltd., Australia
Aristides (Aris) Moustakas, Universiti Brunei Darussalam, Brunei

Copyright © 2018 Krefeld-Schwalb, Witte and Zenker. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Frank Zenker,

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