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OTIS Evaluation Guide (PDF) - California Department of Public Health

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provided to Group A, with no intervention in Group B. After a certain time period, the same intervention<br />

activities are delivered to Group B, with no intervention in Group A. Thus, the original “intervention group” and<br />

“control group” actually switch their roles. Measurements are made at the beginning <strong>of</strong> the program, before the<br />

switching, and after the switching at the end <strong>of</strong> the program.<br />

• Non-experimental designs have the least capability to reflect or demonstrate the success <strong>of</strong> a program.<br />

This type <strong>of</strong> design does not use control groups or random assignment; therefore, at best, it can provide only<br />

a weak indication <strong>of</strong> a possible connection between intervention and outcome. However, it is useful in many<br />

situations when a stronger design is not applicable or the budget is not sufficient.<br />

Let’s look at an example that is not clear-cut in order to illustrate the rationale for determining the appropriate<br />

study design. One <strong>of</strong> the most commonly used designs is a pre- and post-test only with one intervention group.<br />

Difference or change can be detected by comparing the pre- and post-test results. Is this a quasi-experimental<br />

or a non-experimental design? This question is still under debate.<br />

80<br />

• In our opinion, if only one set <strong>of</strong> pre- and post-tests is conducted, the design should be classified as<br />

non-experimental. This is because any number <strong>of</strong> unanticipated events other than the intervention activities<br />

may also produce the desired change, but the design is not capable <strong>of</strong> detecting their influence.<br />

Therefore, extraneous factors cannot be controlled for in the analysis.<br />

• However, if there is more than one pre-test and more than one post-test, the design should be called<br />

quasi-experimental because it uses multiple measurements before, during and after the intervention. In<br />

this situation you virtually treat the only group as both intervention and control group. Any anecdotal<br />

event (other than the intervention activities) that results in a change may be detected during the multiple<br />

measurements. You can determine when the anecdotal event and change occurred, and control for it in<br />

the analysis to determine if the intervention has contributed to this change.<br />

Groups<br />

If you answered “experimental or quasi-experimental” in Figure 19, <strong>OTIS</strong> requests information about the number<br />

<strong>of</strong> intervention and/or control groups, and whether your design contains an intact group (Figure 19):<br />

Number <strong>of</strong> Intervention Groups and Number <strong>of</strong> Control Groups:<br />

To answer this question, consider this scenario: 40 bars in three cities will receive the intervention and 40 bars<br />

in another three cities will receive no intervention. What do you enter for the number <strong>of</strong> intervention groups<br />

and the number <strong>of</strong> control groups? 40? 3?<br />

The answer is “1” intervention group and “1” control group. Multiple intervention groups only exist when<br />

multiple, different intervention strategies are given to different communities. If each <strong>of</strong> these communities has<br />

its own control community, then we have multiple control groups as well.<br />

Intact group:<br />

This strategy is rooted in the same rationale for using intervention groups and control groups, that is, to<br />

increase comparability among different groups. An intact group is the same group <strong>of</strong> people who are<br />

measured with both a pre-test and a post-test. An advantage to using intact groups for experimental or quasi-<br />

<strong>OTIS</strong> <strong>Evaluation</strong> <strong>Guide</strong> • March 2007

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