Skip to content

Pitch Perception and Memory: Deficits and Training

Pitch Perception and Memory: Deficits and Training

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03707691
Acronym
Pitch_Train
Enrollment
960
Registered
2018-10-16
Start date
2019-11-26
Completion date
2027-10-26
Last updated
2025-03-03

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

Conditions

Cochlear Implants

Keywords

Hearing, Cochlear Implants, Congenital Amusia, Pitch, Audio-visual interactions

Brief summary

Pitch perception and memory are central in auditory cognition, in particular for sound source segregation and recognition, speech prosody and music processing. Here the investigator assess pitch perception and memory in hearing-impaired listeners wearing cochlear implant(s) and listeners with congenital amusia, both compared with control listeners. Behavioral, EEG, and MEG measures are collected in audio and audio-visual contexts to characterize pitch processing deficits, and test a pitch training program.

Interventions

BEHAVIORALListening tests. Pitch training protocol

The two training protocols consists of perceptual tasks (auditory or visual exercises) performed repetitively using a tablet. Each protocol consists in 30 sessions of \ 20 minutes performed at home over a period of 15 weeks.

BEHAVIORALvisuo-spatial training protocol

The two training protocols consists of perceptual tasks (auditory or visual exercises) performed repetitively using a tablet. Each protocol consists in 30 sessions of \ 20 minutes performed at home over a period of 15 weeks.

BEHAVIORALEEG/MEG/MRI recordings.

Listening tests. EEG/MEG/MRI recordings

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

For adult participants: * Aged between 18 and 90 * Absence of neurological and psychiatric disorders * No major cognitive deficit, ability to understand and apply study instructions * Motivation to participate efficiently in the study * Written informed consent to participant in the study * Affiliated to social security * Control participants and participants with congenital amusia for Experiment 5: MRI/MEG compatibility For underage participants: * Subject aged 5 years and over * Informed consent of parents or guardians for the participation of the child being studied * No neurological or psychiatric history * Without major cognitive impairment and ability to understand and apply setpoint. * Subject affiliated to a social security scheme * Motivation to participate effectively in the project

Exclusion criteria

For adult participants: * Age below 18 or above 90 * Pregnant or breast-feeding woman For underage participants: \- Pregnant or nursing minors

Design outcomes

Primary

MeasureTime frameDescription
Oscillationsduring procedureMEG measurements
percentages of correct responses in listening testsduring procedure
reaction times in listening testsduring procedure
Event-Related Fieldsduring procedureMEG measurements

Secondary

MeasureTime frameDescription
reaction timesDay 0Performance in listening tests in audio contexts
Event-Related FieldsDay 0EEG measurements
OscillationsDay 0EEG measurements
percentages of correct responsesDay 0Performance in listening tests in audio contexts

Countries

France

Contacts

Primary ContactAnne CACLIN
anne.caclin@inserm.fr4 72 13 89 04
Backup ContactBarbara Tillmann
barbara.tillmann@cnrs.fr4 37 28 74 89

Outcome results

None listed

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