- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07740070
Cognitive Processing of Natural Sequences in Humans and Artificial Intelligence (AI) (SEQUOIA)
SEQUOIA : Cognitive Processing of Natural Sequences in Humans and Artificial Intelligence (AI)
The goal of this study is to identify electrical patterns in the cortex that enable the generation of predictions in natural auditory sequences such as speech and music.
Between 500 and 700 participants in total (250 to 350 normally hearing participants (including 60 to 120 participants from West Africa and 60 to 120 participants from Western Europe) and 250 to 350 participants with hearing loss (no restrictions on origin)).
Participants will listen to naturally recorded music and speech via headphones. They will be asked to rate these stimuli on a scale from 0 to 10 in terms of pleasure and comprehension, using a keyboard and mouse or voice input. Additionally, they will be required to sing or produce novel/improvised vocal responses using high-fidelity microphones. This entire procedure will be conducted under electroencephalography (EEG) to record neuronal responses throughout the process.
Studieöversikt
Status
Betingelser
Studietyp
Inskrivning (Beräknad)
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Testmetod
Studera befolkning
Hearing participants will be recruited from the general population in the Paris region.
We will also recruit participants with hearing impairment through ENT clinics, in hearing aid dispensing centers.
Finally, we will specifically recruit participants residing in Paris and of West African origin to examine differences related to cultural experience.
Beskrivning
Inclusion Criteria:
For hearing participants:
- Average pure-tone thresholds ≤ 20 dB HL
For participants with hearing loss:
- Average pure-tone thresholds > 20 dB HL
For participants of West African origin:
- Average pure-tone thresholds ≤ 20 dB HL
- Declare that both parents are of West African origin, either by their own birth or by the birth of both of their parents.
Exclusion Criteria:
- No known neurological or audiological disorders
- Participants under legal guardianship (tutelle, curatelle)
- Participants deprived of legal liberty by judicial or administrative decision
Studieplan
Hur är studien utformad?
Designdetaljer
Kohorter och interventioner
Grupp / Kohort |
|---|
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Normal hearing participants from West Africa
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Normal hearing participants from Western Europe
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Participants with hearing loss
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Correlation between neural recordings and IA models
Tidsram: Day 1
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To identify electrical patterns in cortex which generates predictions in natural auditory sequences (such as speak and music).
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Day 1
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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Compare predictions generated across different cultural contexts
Tidsram: Day 1
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specifically, comparing West African and Western European communities in Paris
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Day 1
|
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Compare predictions for identical stimuli across repeated sessions to establish a link between processing and successful memorization/retention.
Tidsram: From enrollement to visit 2 (10 days)
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From enrollement to visit 2 (10 days)
|
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Compare predictions generated between hearing individuals and those with hearing impairments.
Tidsram: Day 2
|
Day 2
|
|
|
Correlate predictive measures with responses to autism symptom questionnaires across the various experiments.
Tidsram: Day 1
|
Day 1
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Samarbetspartners och utredare
Sponsor
Samarbetspartners
Studieavstämningsdatum
Studera stora datum
Studiestart (Beräknad)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 2024-102 SEQUOIA
- 2025-A00021-48 (Annan identifierare: ID-RCB)
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
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