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In multi-site cluster-randomized trails (MS-CRTs), participants do not always stay in the same randomly assigned condition nor site. Methodologists have recommended ways to handle condition-switching when estimating a treatment’s effect using, for example, intent-to-treat, per-protocol or as-treated analyses. However, despite methodological research emphasizing the importance of not ignoring cluster-switching through use of the multiple-membership random effects model (MMREM), the inevitable cluster-switching that occurs when participants condition-switch is consistently ignored. The current study details how and why to enhance suggested methods for estimating treatments’ effects when participants change conditions and/or clusters in MS-CRTs by incorporating the MMREM rather than a conventional HLM. Analyses are conducted (pairing each method with each model) using two real datasets. Results are compared and discussed.