Skip to main content
Clinical Trials/NCT03094624
NCT03094624CompletedNot Applicable

Auditory Perceptual and Memory Deficits in Congenital Amusia: Studies of Cerebral Correlates With MEG, Anatomical MRI and Functional MRI

Hospices Civils de Lyon2 sites in 1 country230 target enrollmentStarted: January 13, 2013Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
230
Locations
2
Primary Endpoint
Neurophysiological tests MRI

Study Overview

Brief Summary

The project studies auditory deficits in congenital amusia at the behavioral and neurophysiological levels.

The auditory processes investigated are pitch discrimination, short-term memory, sound-induced emotions. To characterize auditory deficits in the amusic population, neuropsychological assessments are combined with neurophysiological markers (Electro-encephalography: EEG, Magneto-encephalography: MEG, Magnetic Resonance Imaging: MRI).

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Aged from 18 to 70 years' old
  • •Compatibility IRM / MEG (no metal in the body)
  • •Motivation to participate effectively in the project
  • •No neurological or psychiatric history
  • •No severe hearing loss
  • •Informed consent to participate in the study
  • •For Amusic participants: participant diagnosed amusic by the MBEA (Montreal Battery of Evaluation of Amusia)
  • •For Control participants: matched in age, sex, education, music education, laterality, non-amusic (controlled with the MBEA)

Exclusion Criteria

  • •Age below 18 or above 70
  • •Non-Francophone volunteers.
  • •MRI scanning not possible: artificial cardiac pacemaker, insulin pump, metallic prosthesis, intra-cerebral clip, claustrophobia
  • •MEG acquisition not possible: large heads, neurostimulator, metal in the head or the body.
  • •Pregnant or breast-feeding women

Arms & Interventions

Amusia

Experimental

Since 2006, recruitment of amusia participants has been organized in the Lyon region, and some 20 participants (and their matched controls in terms of age, sex, laterality, musical practice, number of years of study) have already taken part various studies conducted at the CRNL. The recruitment of amusia participants and controls is continued in order to maintain a sufficient number of participants and compensate for the withdrawals within the cohort already constituted (lack of availability, geographical distance, etc.).

Intervention: Neuropsychological and neurophysiological tests (Other)

Amusia

Experimental

Since 2006, recruitment of amusia participants has been organized in the Lyon region, and some 20 participants (and their matched controls in terms of age, sex, laterality, musical practice, number of years of study) have already taken part various studies conducted at the CRNL. The recruitment of amusia participants and controls is continued in order to maintain a sufficient number of participants and compensate for the withdrawals within the cohort already constituted (lack of availability, geographical distance, etc.).

Intervention: Experiment 1 (Other)

Amusia

Experimental

Since 2006, recruitment of amusia participants has been organized in the Lyon region, and some 20 participants (and their matched controls in terms of age, sex, laterality, musical practice, number of years of study) have already taken part various studies conducted at the CRNL. The recruitment of amusia participants and controls is continued in order to maintain a sufficient number of participants and compensate for the withdrawals within the cohort already constituted (lack of availability, geographical distance, etc.).

Intervention: Experiment 2 (Other)

Amusia

Experimental

Since 2006, recruitment of amusia participants has been organized in the Lyon region, and some 20 participants (and their matched controls in terms of age, sex, laterality, musical practice, number of years of study) have already taken part various studies conducted at the CRNL. The recruitment of amusia participants and controls is continued in order to maintain a sufficient number of participants and compensate for the withdrawals within the cohort already constituted (lack of availability, geographical distance, etc.).

Intervention: Experiment 3 (Other)

Amusia

Experimental

Since 2006, recruitment of amusia participants has been organized in the Lyon region, and some 20 participants (and their matched controls in terms of age, sex, laterality, musical practice, number of years of study) have already taken part various studies conducted at the CRNL. The recruitment of amusia participants and controls is continued in order to maintain a sufficient number of participants and compensate for the withdrawals within the cohort already constituted (lack of availability, geographical distance, etc.).

Intervention: Experiment 4 (Other)

Matched controls

Sham Comparator

Matched controls of age, sex, laterality, musical practice, number of years of studies.

Intervention: Neuropsychological and neurophysiological tests (Other)

Matched controls

Sham Comparator

Matched controls of age, sex, laterality, musical practice, number of years of studies.

Intervention: Experiment 1 (Other)

Matched controls

Sham Comparator

Matched controls of age, sex, laterality, musical practice, number of years of studies.

Intervention: Experiment 2 (Other)

Matched controls

Sham Comparator

Matched controls of age, sex, laterality, musical practice, number of years of studies.

Intervention: Experiment 3 (Other)

Matched controls

Sham Comparator

Matched controls of age, sex, laterality, musical practice, number of years of studies.

Intervention: Experiment 4 (Other)

Outcomes

Primary Outcomes

Neurophysiological tests MRI

Time Frame: Day 1

MRI images

Neurophysiological tests EEG

Time Frame: Day 1

Event-Related Potentials (EEG)

Correct answers to the neuropsychological tests

Time Frame: Day 1

Percentages of correct responses

Neuropsychological tests reaction times

Time Frame: Day 1

Neuropsychological tests reaction times

Neurophysiological tests MEG

Time Frame: Day 1

Event-Related Fields (MEG)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

Loading locations...

Similar Trials