- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05252312
Perception of Nonverbal Acoustic Signals and Resulting Physiological Responses (SINOVE-PER) (SINOVE-PER)
Perception of Nonverbal Acoustic Signals and Resulting Physiological Responses SINOVE-PER
Like many other animals, humans produce nonverbal signals including screams, grunts, roars, cries and laughter across a variety of contexts.Due to their acoustic structure, nonverbal vocalizations and valanced speech (e.g., yelling) are also likely to elicit predictable physiological, perceptual or behavioural responses in the receiver of the signal (the listener). This is critical if researchers are to gain a comprehensive understanding of the broad range of mechanisms and the evolved functions of acoustic communication.
Therefore, in this research, investigators will examine specifically how exposure to vocal stimuli affects both the cognitive and biological responses of the listener.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Like many other animals, humans produce nonverbal signals including screams, grunts, roars, cries and laughter across a variety of contexts. Many of these signals (such as cries) are already produced at birth and are likely to serve a number of important biological and social functions. In addition, human speech is characterized by nonlinguistic acoustic parameters (such as pitch, formant frequencies, and nonlinear phenomena) that are known to correlate with biologically important traits of the vocalizer.
Due to their acoustic structure, nonverbal vocalizations and valanced speech (e.g., yelling) are also likely to elicit predictable physiological, perceptual or behavioural responses in the receiver of the signal (the listener).
However, while a number of playback studies have examined behavioural responses (e.g., ratings) of listeners when exposed to various voice stimuli, very few studies have examined whether such behavioural responses are accompanied by an underlying physiological response. This is critical if researchers are to gain a comprehensive understanding of the broad range of mechanisms and the evolved functions of acoustic communication.
Therefore, in this research, investigators will examine specifically how exposure to vocal stimuli affects both the cognitive and biological responses of the listener.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: ROLAND PEYRON, MDPhD
- Phone Number: +33 (0)477127805
- Email: roland.peyron@chu-st-etienne.fr
Study Contact Backup
- Name: Nicolas MATHEVON, PhD
- Phone Number: +33 04 77 48 50 22
- Email: nicolas.mathevon@univ-st-etienne.fr
Study Locations
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-
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Saint-Etienne, France, 42055
- Recruiting
- CHU Saint-Etienne
-
Sub-Investigator:
- David REBY, MD PHD
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Sub-Investigator:
- Nicolas MATHEVON, MD PHD
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Principal Investigator:
- Roland PEYRON, MD PHD
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Participant should be affiliated or entitled to a social security scheme
Exclusion Criteria:
- Pregnancy
- Hearing impairment, speech production disorders or major health problems.
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy adult population aged 18 to 80 years
After listening to acoustic stimuli, participants will be asked to judge these stimuli on relevant evaluation criteria (e.g., "how distressed does this person sound?").
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Listeners' cognitive and biological responses to vocal stimuli will be tested using psycho-acoustic tests. After listening to acoustic stimuli, participants will be asked to judge these stimuli on relevant evaluation criteria (e.g., "how distressed does this person sound?"). These stimuli might be human voices, animal voices or synthetic voices Physiological measures will be simultaneously taken using an array of complimentary, non-invasive techniques such as the Nociception Level (NOL) Index or video pupillometry |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Proportion of correct responses in a forced-choice task after vocal stimuli
Time Frame: Immediately after the vocal stimuli
|
Participants will be asked to judge vocal stimuli Example : "Of the two baby cries you listened to, which one do you think shows the most distress"
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Immediately after the vocal stimuli
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Numerical values of judgements along a scale
Time Frame: Immediately after the vocal stimuli
|
Participants will be asked to judge vocal stimuli Example : participants may be asked to judge, along a gradient (from 0 to 100), "how consistent the distress of the baby you heard is to you".
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Immediately after the vocal stimuli
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Response time (second)
Time Frame: Immediately after the vocal stimuli
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Participants will be asked to judge vocal stimuli In this case, the participant is instructed to respond as soon as possible.
The response time for each stimulus is then systematically measured
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Immediately after the vocal stimuli
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heart rate (bpm)
Time Frame: During the vocal stimuli
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During the vocal stimuli
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Skin conductance (Siemens)
Time Frame: During the vocal stimuli
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During the vocal stimuli
|
|
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Skin temperature (°C)
Time Frame: During the vocal stimuli
|
During the vocal stimuli
|
|
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Nociception Level Index (NOL)
Time Frame: During the vocal stimuli
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A non-invasive finger probe, containing four sensors, will be placed on the on the index finger of the participants.
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During the vocal stimuli
|
|
Pupillary diameter (millimeter)
Time Frame: During the vocal stimuli
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Using a high resolution binocular for automated pupil diameter measurement with an infrared camera
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During the vocal stimuli
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: ROLAND PEYRON, MDPHD, CHU de Saint-Etienne
- Study Chair: Nicolas MATHEVON, PhD, University of Saint-Etienne, France
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 20CH151
- 2020-A02993-36 (Other Identifier: ANSM)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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