Actively Recruiting

Phase Not Applicable
Age: 5Years - 90Years
All Genders
Healthy Volunteers
ID03707691

Pitch Perception and Memory: Deficits and Training

Led by Hospices Civils de Lyon · Updated on 2025-03-03

960

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Pitch perception and memory play key roles in how people understand sounds, including recognizing where sounds come from, speech patterns, and music. This research evaluates these abilities in people with hearing impairments who use cochlear implants and those with congenital amusia, comparing them to control participants without these conditions. Researchers aim to better understand pitch processing difficulties and test a new pitch training program. Participants engage in two training protocols that include auditory and visual exercises using a tablet. These protocols involve 30 sessions of about 20 minutes each, performed at home over 15 weeks. The study groups include cochlear implant users, participants with congenital amusia, and control participants. Both pitch and visuo-spatial training protocols are applied to all groups. During the study, various measures are collected such as listening test accuracy and reaction times, as well as brain activity recordings using EEG, MEG, and MRI. These assessments occur both during the training period and at the study's start. The researchers monitor how well participants respond to training and track changes in brain responses related to pitch perception. The study welcomes healthy volunteers aged 5 to 90 years, with participation lasting through the training sessions and associated evaluations.

CONDITIONS

Brief Title

Pitch Perception and Memory: Deficits and Training

Who Can Participate

Age: 5Years - 90Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged between 18 and 90 years
  • No neurological or psychiatric disorders
  • No major cognitive deficits and able to understand and follow study instructions
  • Motivated to participate effectively in the study
  • Provide written informed consent
  • Affiliated with social security
  • Control participants and those with congenital amusia must be compatible with MRI/MEG for Experiment 5
  • Children aged 5 years and older
  • Parental or guardian informed consent for children
  • No neurological or psychiatric history in children
  • Children without major cognitive impairment and able to understand instructions
  • Children affiliated with social security
  • Motivated to participate effectively in the study
Not Eligible

You will not qualify if you...

  • Adults younger than 18 or older than 90 years
  • Pregnant or breastfeeding women
  • Pregnant or nursing minors

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 15 weeks

Participants perform two training protocols consisting of auditory and visual perceptual tasks using a tablet at home.

30 sessions of approximately 20 minutes each performed at home

Outpatient Treatment

Duration - 15 weeks

Participants perform a visuo-spatial training protocol involving repetitive perceptual tasks using a tablet at home.

30 sessions of approximately 20 minutes each performed at home

Outpatient Treatment

Duration - During the treatment period

Participants undergo EEG/MEG/MRI recordings and listening tests as part of the study assessments.

Visit schedule depends on sessions; specifics not provided

Trial Site Locations

Total: 1 location

1

Lyon Neuroscience Research Center

Bron, France, 69500

Actively Recruiting

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Research Team

A

Anne CACLIN

B

Barbara Tillmann

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

3

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