# Crossover study

A **crossover study**, also referred to as a **crossover trial**, is a longitudinal study in which subjects receive a sequence of different treatments (or exposures). While crossover studies can be observational studies, many important crossover studies are controlled experiments, which are discussed in this article. Crossover designs are common for experiments in many scientific disciplines, for example psychology, education, pharmaceutical science, and medicine.

Randomized, controlled crossover experiments are especially important in health care. In a randomized clinical trial, the subjects are randomly assigned to different arms of the study which receive different treatments. When the randomized clinical trial is a repeated measures design, the same measures are collected multiple times for each subject. A crossover clinical trial is a repeated measures design in which each patient is randomly assigned to a sequence of treatments, including at least two treatments (of which one "treatment" may be a standard treatment or a placebo).

Nearly all crossover designs have "balance", which means that all subjects should receive the same number of treatments and that all subjects participate for the same number of periods. In most crossover trials, in fact, each subject receives all treatments.

Statisticians suggest that designs have four periods, a design which allows studies to be truncated to three periods while still enjoying greater efficiency than the two-period design.^{[1]}^{[2]} However, the two-period design is often taught in non-statistical textbooks, partly because of its simplicity.

## Contents

## Clinical trial protocol specifies the statistical analysis

The data are analyzed using the statistical method that was specified in the clinical trial protocol, which needs to have been approved by the appropriate institutional review boards and regulatory agencies **before** the trial could begin. Again, the clinical trial protocols specify the method of statistical analysis. Most clinical trials are analyzed using repeated-measurements anova (analysis of variance) or mixed models that include random effects.

In most longitudinal studies of human subjects, patients may withdraw from the trial or become "lost to follow-up" (due e.g. to moving abroad or to dying from another disease). There are statistical methods for dealing with such missing-data and "censoring" problems. An important method analyzes the data according to the principle of the intention to treat.

## Advantages

A crossover study has two advantages over both a parallel study and a non-crossover longitudinal study. First, the influence of confounding covariates is reduced because each crossover patient serves as his or her own control^{[citation needed]}. In a non-crossover study, even randomized, it is often the case that different treatment-groups are found to be unbalanced on some covariates. In a controlled, randomized crossover designs, such imbalances are implausible (unless covariates were to change systematically during the study).

Second, optimal crossover designs are statistically efficient and so require fewer subjects than do non-crossover designs (even other repeated measures designs).

Optimal crossover designs are discussed in the graduate textbook by Jones and Kenward and in the review article by Stufken. Crossover designs are discussed along with more general repeated-measurements designs in the graduate textbook by Vonesh and Chinchilli.

## Limitations and disadvantages

These studies are often done to improve the symptoms of patients with chronic conditions. For curative treatments or rapidly changing conditions, cross-over trials may be infeasible or unethical.

Crossover studies often have two problems:

First is the issue of "order" effects, because it is possible that the order in which treatments are administered may affect the outcome. An example might be a drug with many adverse effects given first, making patients taking a second, less harmful medicine, more sensitive to any adverse effect.

Second is the issue of "carry-over" between treatments, which confounds the estimates of the treatment effects. In practice, "carry-over" effects can be avoided with a sufficiently long "wash-out" period between treatments. However, planning for sufficiently long wash-out periods requires expert knowledge of the dynamics of the treatment, which is often unknown.

Also, there might be a "learning" effect. This is important where you have controls who are naive to the intended therapy. In such a case e.g. you cannot make a group (typically the group which learned the skill first) unlearn a skill such as yoga and then act as a control in the second phase of the study.

## See also

This article includes a list of references, related reading or external links, but its sources remain unclear because it lacks inline citations. (April 2013) |

## Notes

## References

- M. Bose and A. Dey (2009).
*Optimal Crossover Designs*. World Scientific. ISBN 978-9812818423 - D. E. Johnson (2010). Crossover experiments.
*WIREs Comp Stat*, 2: 620-625. [1] - Jones, Byron; Kenward, Michael G. (2003).
*Design and Analysis of Cross-Over Trials*(Second ed.). London: Chapman and Hall. ISBN 0412606402. - Najafi Mehdi, (2004).
*Statistical Questions in Evidence Based Medicine*. New York: Oxford University Press. ISBN 0-19-262992-1 - D. Raghavarao and L. Padgett (2014).
*Repeated Measurements and Cross-Over Designs.*Wiley. ISBN 978-1-118-70925-2 - D. A. Ratkowsky, M. A. Evans, and J. R. Alldredge (1992).
*Cross-Over Experiments: Design, Analysis, and Application.*Marcel Dekker. ISBN 978-0824788926 - Senn, S. (2002).
*Cross-Over Trials in Clinical Research,*Second edition. Wiley. ISBN 978-0-471-49653-3 - Stufken, J. (1996). "Optimal Crossover Designs". In Ghosh, S. and Rao, C. R.
*Design and Analysis of Experiments*. Handbook of Statistics.**13**. North-Holland. pp. 63–90. ISBN 0-444-82061-2. - Vonesh, Edward F.; Chinchilli, Vernon G. (1997). "Crossover Experiments".
*Linear and Nonlinear Models for the Analysis of Repeated Measurements*. London: Chapman and Hall. pp. 111–202. ISBN 0824782488.