"A value-added analysis constitutes a series of personal, high-stakes experiments conducted under extremely uncontrolled conditions".
If drug experiments were conduted like VAM we might all have 3 legs or worse
Another scientific school of thought, especially prevalent in medical research, holds that the most reliable method for arriving at defensible causal conclusions involves conducting randomized controlled trials, or RCTs, in which (a) individuals are premeasured on an outcome, (b) randomly assigned to receive different treatments, and (c) measured again to ascertain if changes in the outcome differed based upon the treatments received.
The purpose of this brief essay is not to argue the pros and cons of the two approaches, but to frame value-added teacher evaluation from the latter, experimental perspective. For conceptually, what else is an evaluation of perhaps 500 4th grade teachers in a moderate-size urban school district but 500 high-stakes individual experiments? Are not students premeasured, assigned to receive a particular intervention (the teacher), and measured again to see which teachers were the more (or less) efficacious?
Granted, a number of structural differences exist between a medical randomized controlled trial and a districtwide value-added teacher evaluation. Medical trials normally employ only one intervention instead of 500, but the basic logic is the same. Each medical RCT is also privy to its own comparison group, while individual teachers share a common one (consisting of the entire district's average 4th grade results).
From a methodological perspective, however, both medical and teacher-evaluation trials are designed to generate causal conclusions: namely, that the intervention was statistically superior to the comparison group, statistically inferior, or just the same. But a degree in statistics shouldn't be required to recognize that an individual medical experiment is designed to produce a more defensible causal conclusion than the collected assortment of 500 teacher-evaluation experiments.
How? Let us count the ways:
- Random assignment is considered the gold standard in medical research because it helps to ensure that the participants in different experimental groups are initially equivalent and therefore have the same propensity to change relative to a specified variable. In controlled clinical trials, the process involves a rigidly prescribed computerized procedure whereby every participant is afforded an equal chance of receiving any given treatment. Public school students cannot be randomly assigned to teachers between schools for logistical reasons and are seldom if ever truly randomly assigned within schools because of (a) individual parent requests for a given teacher; (b) professional judgments regarding which teachers might benefit certain types of students; (c) grouping of classrooms by ability level; and (d) other, often unknown, possibly idiosyncratic reasons. Suffice it to say that no medical trial would ever be published in any reputable journal (or reputable newspaper) which assigned its patients in the haphazard manner in which students are assigned to teachers at the beginning of a school year.
- Medical experiments are designed to purposefully minimize the occurrence of extraneous events that might potentially influence changes on the outcome variable. (In drug trials, for example, it is customary to ensure that only the experimental drug is received by the intervention group, only the placebo is received by the comparison group, and no auxiliary treatments are received by either.) However, no comparable procedural control is attempted in a value-added teacher-evaluation experiment (either for the current year or for prior student performance) so any student assigned to any teacher can receive auxiliary tutoring, be helped at home, team-taught, or subjected to any number of naturally occurring positive or disruptive learning experiences.
- When medical trials are reported in the scientific literature, their statistical analysis involves only the patients assigned to an intervention and its comparison group (which could quite conceivably constitute a comparison between two groups of 30 individuals). This means that statistical significance is computed to facilitate a single causal conclusion based upon a total of 60 observations. The statistical analyses reported for a teacher evaluation, on the other hand, would be reported in terms of all 500 combined experiments, which in this example would constitute a total of 15,000 observations (or 30 students times 500 teachers). The 500 causal conclusions published in the newspaper (or on a school district website), on the other hand, are based upon separate contrasts of 500 "treatment groups" (each composed of changes in outcomes for a single teacher's 30 students) versus essentially the same "comparison group."
- Explicit guidelines exist for the reporting of medical experiments, such as the (a) specification of how many observations were lost between the beginning and the end of the experiment (which is seldom done in value-added experiments, but would entail reporting student transfers, dropouts, missing test data, scoring errors, improperly marked test sheets, clerical errors resulting in incorrect class lists, and so forth for each teacher); and (b) whether statistical significance was obtained—which is impractical for each teacher in a value-added experiment since the reporting of so many individual results would violate multiple statistical principles.
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