Lucid dreaming, where a person becomes aware they are dreaming, is linked to REM sleep. To overcome previous research limitations, a new preprocessing pipeline was applied to pooled EEG data from multiple labs. Sensor-level differences between lucid and nonlucid REM sleep were minimal, but source-level analysis revealed reduced beta power (12-30 Hz) in right central and parietal areas, including the temporoparietal junction, during lucid dreaming. Alpha-band (8-12 Hz) connectivity increased compared to nonlucid REM sleep. During eye signaling of lucidity, gamma1 power (30-36 Hz) increased in right temporo-occipital regions, including the precuneus, and interhemispheric gamma1 connectivity rose. These patterns suggest shifts in network communication underlying changes in perception, self-awareness, and cognitive control.
Lucid dreaming, a state of conscious awareness during REM sleep, is associated with specific brain activity patterns. Compared to non-lucid REM sleep, EEG sensor-level differences were few. However, source-level analysis revealed increased gamma1 power (30-36 Hz) in left-hemispheric temporal areas during lucid dreaming, potentially reflecting verbal insight processes, and in right temporo-occipital regions including the precuneus around the onset of lucid eye signaling, linked to self-referential thinking. Beta power (12-30 Hz) decreased in right central and parietal areas including the temporo-parietal junction, possibly related to conscious reality assessment. Alpha-band (8-12 Hz) functional connectivity increased, contrasting with psychedelic states and highlighting enhanced self-awareness.