The N-of-1 trials can be designed in many ways. For example, Single-Patient Open Trials (SPOTs) are located somewhere in between the formal (explanatory) N-of-1 trials and the trial and error approach used in clinical practice and are characterized by at least one crossover period with washout in between. One of the most common procedures is the ABA withdrawal experimental design, where the patient problem is measured before a treatment is introduced (baseline) and then measured again during the treatment and finally when the treatment has terminated. If the problem vanished during the treatment it can be established that the treatment was effective. But the N=1 study can also be executed in an AB
quasi experimental way; such type-2 N-of-1 studies can be effective for testing treatments for severe, rare diseases when the expected effect of the intervention exceeds the effect size of confounders. Another variation is non-concurrent experimental design where different points in time are compared with one another. The standard approach to therapy choice, the
trial and error method, may also be included in the N-of-1 design. This experimental design also has a problem with causality, whereby statistical significance under a
frequentist paradigm may be un-interpretable but other methods, such as clinical significance or
Bayesian methods should be considered. Many consider this framework to be a proof of concept or hypothesis generating process to inform subsequent, larger clinical trials. ==List of variation in N-of-1 trial==