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

Recruiting

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

Observational

Enrollment (Estimated)

2000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Saint-Etienne, France, 42055
        • Recruiting
        • CHU Saint-Etienne
        • Sub-Investigator:
          • David REBY, MD PHD
        • Sub-Investigator:
          • Nicolas MATHEVON, MD PHD
        • Principal Investigator:
          • Roland PEYRON, MD PHD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Healthy adult population aged 18 to 80 years

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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?").

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
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"
Immediately after the vocal stimuli
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".
Immediately after the vocal stimuli
Response time (second)
Time Frame: Immediately after the vocal stimuli
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
Immediately after the vocal stimuli

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Heart rate (bpm)
Time Frame: During the vocal stimuli
During the vocal stimuli
Skin conductance (Siemens)
Time Frame: During the vocal stimuli
During the vocal stimuli
Skin temperature (°C)
Time Frame: During the vocal stimuli
During the vocal stimuli
Nociception Level Index (NOL)
Time Frame: During the vocal stimuli
A non-invasive finger probe, containing four sensors, will be placed on the on the index finger of the participants.
During the vocal stimuli
Pupillary diameter (millimeter)
Time Frame: During the vocal stimuli
Using a high resolution binocular for automated pupil diameter measurement with an infrared camera
During the vocal stimuli

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: ROLAND PEYRON, MDPHD, CHU de Saint-Etienne
  • Study Chair: Nicolas MATHEVON, PhD, University of Saint-Etienne, France

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 29, 2022

Primary Completion (Estimated)

April 1, 2027

Study Completion (Estimated)

April 1, 2027

Study Registration Dates

First Submitted

February 2, 2022

First Submitted That Met QC Criteria

February 11, 2022

First Posted (Actual)

February 23, 2022

Study Record Updates

Last Update Posted (Actual)

May 6, 2026

Last Update Submitted That Met QC Criteria

May 5, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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