RES 4353 Module 4 Interpretation of Statistical Results Example

Reviewed by Hollis Fairweather, PhD · American College of Education · Updated

This RES 4353 Module 4 example is a complete interpretation of statistical results, in APA 7, from Yin and colleagues' 2014 study of 287 parents and the units on their children's liquid medicine instructions. It was written for American College of Education RES 4353, Evidence-based Health Education and Literacy, the ACE course RES4353 in the B.S. in Healthcare Administration. The paper moves in order: error rates of 42.5% with teaspoons against 27.6% with milliliters, a number needed to treat near seven, p-values of .02 and .04, and adjusted odds ratios of 2.3 and 1.9 with their covariates. It then converts those odds ratios to relative risks of about 1.7 and 1.5 with Zhang and Yu's method, reads wide confidence intervals, and explains effect modification and kitchen-spoon mediation before setting the result beside Yin's 2017 experiment. Many sections assign the study.

CourseRES 4353 Evidence-based Health Education and Literacy
ModuleModule 4
Paper typeInterpretation of statistical results
Length1,180 words, about 4 pages plus title and reference pages
FormatAPA 7 student paper
SchoolAmerican College of Education
ProgramB.S. in Healthcare Administration
UpdatedSeptember 2026

Free sample paper for RES 4353 Module 4

1

Twice the Odds Is Not Twice the Risk: Interpreting the Statistics in a Study of Teaspoon Units and Parents' Dosing Errors

Student Name

American College of Education

RES4353: Evidence-based Health Education and Literacy

Module 4 Assignment

Instructor Name

October 26, 2026

What this page is doingThe title states the most common misreading the paper corrects, which tells the grader the interpretation goes beyond repeating the authors' numbers. The APA 7 title page carries the course line and the module assignment as listed.
2

The Study and Its Headline

Earlier modules in this course examined the evidence behind a community health center pharmacy's plan to print liquid medicine doses in milliliters only. One of the key studies, by Yin et al. (2014), studied 287 parents, English or Spanish speaking, who left one of two emergency departments with a liquid medicine for their child, and asked whether the unit written on the instructions, milliliters or teaspoons and tablespoons, was associated with dosing errors. An error was defined as a measured dose more than 20% away from the intended or prescribed dose. The headline, repeated in later citations, is that teaspoon and tablespoon instructions came with twice the odds of an error.

A pharmacy manager reading that headline might conclude that switching units would halve errors. This paper works through the study's statistics in order, from simple percentages to adjusted odds ratios, confidence intervals, subgroup differences and mediation, to show what the numbers do and do not support.

What this page is doingThe paper sets out the study, its outcome definition and the headline claim, and it frames the interpretation around a realistic misreading by a decision maker.
3

Starting With the Percentages

The simplest numbers are often the most useful. Overall, 39.4% of parents measured the intended dose incorrectly, and 41.1% made an error against the prescribed dose. Among parents using teaspoon or tablespoon units, 42.5% made an error with the intended dose, compared with 27.6% of parents using milliliters only. The comparable figures for the prescribed dose were 45.1% and 31.4%.

Two things stand out before any modeling. First, errors were common in both groups; even with milliliters only, more than a quarter of parents measured incorrectly, so no change of units alone would eliminate the problem. Second, the absolute difference for the intended dose was about 15 percentage points. Put in terms a manager can use, if the unit difference were fully causal, switching roughly seven parents from teaspoons to milliliters would prevent one error, since one divided by 0.149 is about 6.7.

What this page is doingRaw percentages are interpreted first, including the absolute difference and a number-needed-to-treat style calculation, which grounds the later ratios.
4

P-Values

The study reports P = .02 for the difference in intended-dose errors and P = .04 for prescribed-dose errors. The p-value speaks to one limited matter: if the two groups truly made errors at the same rate, how often would a gap this big or bigger turn up by chance alone? Values below the conventional .05 threshold are called statistically significant. They do not measure how large or important a difference is, and a value of .04 is only just below the line. The p-values say that chance alone is an unlikely explanation for the gaps; they say nothing about whether a gap of this size matters, which is the question the confidence interval and the percentages answer better.

What this page is doingThe p-value is defined correctly and its limits are explained, including what it does not measure, which is a common source of error in interpretation.
5

Adjusted Odds Ratios

The headline figures are adjusted odds ratios from multiple logistic regression: 2.3 for the intended dose and 1.9 for the prescribed dose. Odds are the probability of an event divided by the probability of it not happening, so an error rate of 42.5% corresponds to odds of about 0.74. An odds ratio compares the odds in two groups. Adjustment means the model estimated the association while holding constant parent age, language, country of origin, race and ethnicity, socioeconomic status, education, health literacy, child age, chronic disease and study site. That matters because parents who use teaspoons might differ in other ways, such as education or language, that also affect errors.

The point most readers miss is that odds ratios exaggerate relative risk when the outcome is common. Zhang and Yu (1998) described a method for converting an odds ratio into an approximate relative risk using the outcome rate in the comparison group. Applying it with the 27.6% error rate among milliliter users, an adjusted odds ratio of 2.3 corresponds to a relative risk of about 1.7. For the prescribed dose, 1.9 becomes about 1.5. Twice the odds, in a study where errors are this common, means roughly 50% to 70% more errors, not twice as many.

What this page is doingOdds and odds ratios are defined, the adjustment variables are listed with their purpose, and the ratios are converted to approximate relative risks with a cited method.
6

Confidence Intervals

Each adjusted odds ratio comes with a 95% confidence interval: 1.2 to 4.4 for the intended dose and 1.03 to 3.5 for the prescribed dose. The interval gives the range of values compatible with the data, and because both exclude 1.0, the value meaning no association, both results are statistically significant, consistent with the p-values. But the intervals are wide. The true intended-dose odds ratio could be as small as 1.2, a modest association, or as large as 4.4. The prescribed-dose interval nearly touches 1.0. With 287 parents split across unit groups, the study was large enough to detect an association but not to pin down its size precisely. A practical way to use such an interval is to plan around its lower end. If the pharmacy's case for milliliter-only labels still holds when the association is as weak as an odds ratio of 1.2, the decision does not depend on the study's imprecision; if the case would collapse at that value, the manager should look for stronger evidence before investing. Here the change costs little, since the pharmacy only needs to alter a label template, so even the modest end of the interval is enough to justify it.

What this page is doingConfidence intervals are interpreted for both significance and precision, and the width is connected to sample size, which is the key skill in reading them.
7

Subgroups and Mediation

The authors report that the associations were greater for parents with low health literacy and for those who did not speak English. When the effect of one factor differs across levels of another, it is called effect modification or interaction. For the pharmacy, it means the families most at risk are likely to benefit most from milliliter-only labels, which strengthens the case for the change in a clinic where many families speak Spanish.

The study also found that use of nonstandard instruments, such as kitchen spoons, partly mediated the association. Mediation means that part of the effect of teaspoon units on errors travels through a pathway: teaspoon units lead some parents to reach for a kitchen spoon, and kitchen spoons lead to errors. Because the mediation was partial, some of the association remains even among parents using proper tools. The practical lesson is that milliliter labels and a proper dosing tool work on the same pathway, and providing both is sensible.

What this page is doingEffect modification and mediation are defined in plain language and each is translated into a practical implication for the pharmacy's decision.
8

Observational Estimates Versus Experimental Ones

Because the 2014 study was cross-sectional, its odds ratios describe association, not effect, even after adjustment, since unmeasured differences between prescribers or families could remain. A later randomized experiment by the same group offers a check. When parents were randomly assigned labels and tools, those given milliliter-and-teaspoon labels made more errors than those given milliliter-only labels, with an adjusted odds ratio of 1.3 and a confidence interval of 1.05 to 1.6 (Yin et al., 2017). The experimental estimate is smaller than the observational one, which is a common pattern when confounding inflates associations, and it concerns a measuring task rather than home dosing. Read together, the two studies suggest a real but moderate benefit from milliliter-only labeling, larger for the families with the fewest advantages, and best delivered alongside syringes and clear instructions. That is the conclusion the final evidence brief should carry to the pharmacy.

What this page is doingThe observational estimate is compared with an experimental one, the difference in size is explained, and the paper ends with a calibrated conclusion for the decision maker.
9

References

Yin, H. S., Dreyer, B. P., Ugboaja, D. C., Sanchez, D. C., Paul, I. M., Moreira, H. A., Rodriguez, L., & Mendelsohn, A. L. (2014). Unit of measurement used and parent medication dosing errors. Pediatrics, 134(2), e354-e361. https://doi.org/10.1542/peds.2014-0395

Yin, H. S., Parker, R. M., Sanders, L. M., Mendelsohn, A., Dreyer, B. P., Bailey, S. C., Patel, D. A., Jimenez, J. J., Kim, K.-Y. A., Jacobson, K., Smith, M. C. J., Hedlund, L., Meyers, N., McFadden, T., & Wolf, M. S. (2017). Pictograms, units and dosing tools, and parent medication errors: A randomized study. Pediatrics, 140(1), Article e20163237. https://doi.org/10.1542/peds.2016-3237

Zhang, J., & Yu, K. F. (1998). What's the relative risk? A method of correcting the odds ratio in cohort studies of common outcomes. JAMA, 280(19), 1690-1691. https://doi.org/10.1001/jama.280.19.1690

The RES 4353 Module 4 assignment instructions

In many sections, the RES 4353 Module 4 prompt has you explain the statistics in a published health study as if to a practitioner who must act on them. Prompts typically ask you to identify the statistical tests used, report and interpret key results such as means, percentages, p-values, odds or risk ratios and confidence intervals, distinguish statistical from practical significance, and discuss what the results mean for practice. Some versions ask you to calculate a simple measure, such as an absolute difference or number needed to treat. Others ask about limitations of the analysis. Choose a study whose results section you can follow, often one from your earlier search, and check Canvas for whether you should include a table of the results you interpret.

How the RES 4353 Module 4 example is put together

The worked interpretation opens with the study, its outcome definition and the headline a manager is likely to misread. It starts with raw percentages and turns the absolute difference into a number needed to treat. P-values are defined and their limits explained. The adjusted odds ratios come next, with a definition of odds, the list of adjustment variables and a conversion to approximate relative risk using a published method. Confidence intervals are read for precision as well as significance. Subgroup differences and mediation are each defined and applied to the pharmacy's families. A final section compares the observational estimate with an experimental one and ends with the calibrated conclusion the evidence brief will carry.

RES 4353 Module 4 rubric: what full marks look like

Statistics interpretation rubrics usually reward accurate definitions, correct interpretation of each result and translation into practical meaning. The accuracy criterion checks that p-values, odds ratios and confidence intervals are described correctly; misdefining a p-value is among the most common deductions. Interpretation earns full credit when the paper distinguishes statistical from practical significance and comments on precision. Graders reward calculations such as absolute differences or number needed to treat when they are done correctly. A criterion on limitations often asks about study design and confounding. Clear explanation for a nonspecialist reader is valued throughout. Correct citation in APA 7 finishes the rubric.

RES 4353 Module 4 help: mistakes that cost points

Interpretation papers lose the most points by saying a p-value is the probability the result is due to chance, or that a significant result is an important one. Another frequent error is reading an odds ratio of 2 as twice the risk when the outcome is common. Students also ignore confidence intervals or mention them without explaining what their width means. Start with the raw numbers before the model results. Say what adjustment does and does not accomplish. Translate every statistic into a sentence a manager could act on. Should your study report means, hazard ratios or correlations instead, share it with your prompt, and we can write a Module 4 interpretation of those results.

Write yours, or have the desk draft it

This paper is an original model document written by our desk, not a submitted student paper and not an official American College of Education document. Read it for the moves, then write your own to the instructions in your classroom. If you want one built to your exact prompt and rubric, the first custom sample is free and arrives in 24 to 48 hours.

More RES 4353 and B.S. in Healthcare Administration sample papers

RES 4353 Module 4 questions, answered

What does RES4353 Module 4 usually ask for?

In many sections, the fourth RES4353 module asks you to interpret the statistical results of a health study, such as percentages, p-values, odds ratios and confidence intervals, and to explain what they mean for practice. Your classroom's instructions decide the study.

Is an odds ratio the same as a relative risk?

No. When an outcome is rare they are similar, but when it is common, as with many health behaviors, the odds ratio overstates the relative risk. It can be converted to an approximate relative risk using the baseline rate.

What does a 95% confidence interval tell you?

The range of values compatible with the data. If it excludes the no-effect value, the result is statistically significant; its width shows how precisely the effect is estimated.

Where can I find a free RES 4353 Module 4 sample paper?

It is posted in full on this page: the Module 4 interpretation of a study on teaspoon units and dosing errors, covering percentages, p-values, adjusted odds ratios converted to relative risk, confidence intervals, subgroups and mediation.

What is the difference between effect modification and mediation?

Effect modification means an association differs across groups, such as by health literacy. Mediation means part of an effect works through an intermediate step, such as teaspoon units leading to kitchen spoon use.