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Sleep and Rehearsal-Driven Memory in Epilepsy

Rehearsal-Induced Memory Consolidation and Its Modulation by Sleep in People With Epilepsy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06967935
Acronym
CORESOM-EPI
Enrollment
20
Registered
2025-05-13
Start date
2025-06-30
Completion date
2026-07-31
Last updated
2025-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epilepsy, Memory Consolidation

Keywords

Epilepsy, Memory consolidation, Sleep, Reharsal, Reactivation

Brief summary

Memory consolidation transforms unstable memory traces into lasting representations, a process enhanced by both sleep and rehearsal during learning. Rehearsal is thought to accelerate consolidation by inducing memory reactivations that resemble those occurring during sleep. However, the respective mechanisms of sleep- and rehearsal-induced consolidation-and their potential interactions-remain poorly understood, especially in patients with temporal lobe epilepsy, where rehearsal might help compensate for memory deficits linked to hippocampal dysfunction, and where sleep may exacerbate epileptic activity. The CORESOM-EPI study aims to compare the effects of rehearsal and sleep on memory consolidation in patients undergoing video-EEG monitoring. Participants will learn object-place associations under two conditions (single versus repeated encoding), with memory tested immediately and again after a 12-hour delay. This delay will either include a full day awake or a night of sleep, allowing direct comparison of sleep- and rehearsal-related consolidation effects. Each participant will perform the task twice, with wake and sleep condition, in a balanced order. As a preliminary phase of the CRIMES study (ANR-DFG 2024), CORESOM-EPI will help assess how sleep and rehearsal influence memory consolidation in epilepsy. It will also serve to adapt the behavioral task for clinical use, paving the way for a future intracranial EEG investigations that will explore the neural networks involved and their modulation by epileptic activity.

Interventions

OTHERCognitive memory task on a computer

Encoding: (1) Participants will learn 60 associations between pairs of items (cue and target) that are presented sequentially at unique locations on a screen, in a given context. 30 pairs are presented once, and 30 pairs are presented repeatedly (4 times). (2) After learning, the first recall phase begins after a short delay of 30 minutes: 50% of the pairs are tested in a similar way, this time with an assessment of contextual memory. (3) The remaining 50% of pairs are tested after a 12-hour delay, involving either a day awake (condition 1) or a night asleep (condition 2).

Eye-tracking will be carried out during the task to ensure that participants are focused on the task (quantification of the number and duration of eye fixations in the area of interest corresponding to the target presentation)

OTHERQuestionnaires on task-related fatigue

Questionnaire on task-related fatigue (Likert-scale) will be completed by participants between blocks of items during the task

OTHERQuestionnaire on task difficulty

Questionnaires on task difficulty (Likert-scale) will be completed by participants at the end of the task

OTHERKarolinska scale

Participants' state of sleepiness will be assessed at the beginning of each stage (encoding, immediate recall, delayed recall) using the Karolinska sleepiness scale

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patient with epilepsy (any type of epilepsy) * Hospitalized for video-EEG recording lasting at least 4 days * Aged 18-65 years

Exclusion criteria

* Major cognitive impairment other than memory deficit * Refusal to participate * Pregnant women, women in labor or nursing mothers * Persons deprived of their liberty by judicial or administrative decision * Persons under psychiatric care * Persons admitted to a health or social institution for purposes other than research * Adults under legal protection (guardianship, curatorship)

Design outcomes

Primary

MeasureTime frameDescription
Change in the percentage of object categories recalled (vs. not recalled) between immediate (30 min after learning) and delayed (12h after learning) recall for rehearsed versus non-rehearsed items.Day 2The impact of rehearsal on object category recognition in an object-place learning paradigm is assessed. For the primary outcome, data from the 2 conditions (wake and sleep during the 12h period between immediate and delayed recall) will be pooled. Each participant will take part in the wake and sleep condition over 4 days (2 conditions separated by at least 24h), in a balanced order between participants.

Countries

France

Contacts

Primary ContactLaure PETER-DEREX, Professor
laure.peter-derex@chu-lyon.fr+334 72 07 17 69
Backup ContactSylvain Rheims, Professor
sylvain.rheims@chu-lyon.fr+334 72 45 79 00

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026