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Language and Brain Rhythms

Language and Brain Rhythms

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04457622
Acronym
LaBRhythms
Enrollment
264
Registered
2020-07-07
Start date
2021-02-18
Completion date
2026-03-16
Last updated
2026-08-20

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

Conditions

Healthy Volunteers

Keywords

Auditory Perception, Speech, Neuroimaging

Brief summary

For humans and other animals, predicting the timing of sensory events is essential for their daily behavior. Importantly, natural sensory stimulation (such as movements, music, or speech) can present temporal regularities allowing for temporal prediction of incoming sensory information. For instance, individuals can easily predict in time the next step of a walker, or the next beat of a song based on the rhythm. The phenomenon of temporal prediction has for now only been investigated experimentally in deterministic scenarios, i.e. when the duration between two sensory events is fixed, or when stimuli present a regular beat. The objective of this project is to understand how we process more natural, hence more complex forms of temporal regularities, and how individuals make inferences on the timing of sensory events based on past temporal statistics of sensory information. This is particularly important for speech processing, considering that speech is an acoustic signal that is known to possess some form of temporal regularity, and yet is not purely rhythmic nor does have a deterministic temporal structure. Temporal regularities are specific to each spoken language, and both native and non-native language listeners are known to use temporal acoustic cues during speech listening. This affects speech comprehension and has a strong impact during language learning. Hence, understanding the processing of temporal regularities in speech can help improve language abilities in first and second language learners. The project is composed of four experiments. The first behavioral experiment will investigate how auditory perception is affected by the temporal statistics of past sensory information using artificial stimuli. The second axis will investigate the neural mechanisms underlying auditory timing processing with electroencephalography (EEG). The last Magnetoencephalography (MEG, experiment 3) and EG (rxperiement 4) experiment will test the role of temporal statistics in an ecological setting, namely speech listening. The project will thus provide strong theoretical advances as it will give new insights on brain mechanisms for the processing of complex temporal information in audition and speech, and their role in language comprehension. It will also provide methodological advances. Specifically, the project will contribute to the development and validation of cutting-edge methods in MEG. Namely, it will aim at creating new tools to investigate the neural correlates of auditory and speech processing with an unprecedented temporal and spatial resolution.

Interventions

OTHERAuditory perception tasks in healthy participants

The participants complete auditory perception tasks while EEG, and MEG record brain signals (primary outcome measure). The tasks acquire behavioral responses with button presses (secondary outcome measure). All analyses are intra-subject (no analyses are between-subject).

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

For all experiments: * 18- 40 years old * Registration with the French healthcare system * Informed consent * Normal hearing Additionally, for experiments 2,3 and 4 : \- Right handed Additionally, for experiment 3 and 4: \- French as native language

Exclusion criteria

For All Experiments: * Neurological or psychiatric illnesses or a history of such problems that could impact quality/variability of data or cooperation and retention of the subject in the study * Regular use of medications that impact the central nervous system * Regular use of medications, such as opioids and antidepressants, including SSRIs and tricyclic antidepressants * Severe hearing loss * A history of stroke or recent trauma to the head * Persons unable to adhere to abstinence from the use of drugs or alcohol the day or evening before experimental sessions * Women who are pregnant, breastfeeding, or have given birth in the last 6 months Additionally, for experiment 2,3 and 4 : * A pacemaker, insulin or other pump, neurostimulator, cochlear implants or other hearing aid, metal stents, prosthesis, or implants, intracerebral clips, implantable defibrillator, cerebral shunt or ventricular catheter, other foreign metal objects in the upper part of the body * any dental apparatus containing metal including or root canals * any foreign metallic object anywhere in the body * bolts, screws * orthopedic devices or implants Additionally, for experiment 3 and 4: * claustrophobia * glasses (given the participant cannot use contact lenses) * a head size incompatible with the use of a personalized 3D headcast or a magnetoencephalography * Persons having had any surgery prior to the study which puts them at risk for metal objects left in the body

Design outcomes

Primary

MeasureTime frame
Stimulus-Brain (EEG) Coherence in the delta-theta range (1 Hz - 8 Hz)at max 90 days
Amplitude of EEG evoked responses to the target stimuliat max 90 days
Stimulus-Brain (MEG) Coherence in the delta-theta range (1 Hz - 8 Hz)at max 90 days
Amplitude of MEG evoked responses to the target stimuliat max 90 days

Secondary

MeasureTime frameDescription
Percentage of correct responsesat max 90 daysThe secondary outcome measures will be recorded in all experiments
Response Timesat max 90 daysThe secondary outcome measures will be recorded in all experiments

Countries

France

Contacts

PRINCIPAL_INVESTIGATORAnne KOSEM, PhD

Centre de recherche de Neurosciences de Lyon (CRNL)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 21, 2026