Perception of Nonverbal Acoustic Signals and Resulting Physiological Responses (SINOVE-PER)
SINOVE-PER
2 other identifiers
observational
2,000
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Nov 2022
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 2, 2022
CompletedFirst Posted
Study publicly available on registry
February 23, 2022
CompletedStudy Start
First participant enrolled
November 29, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
April 1, 2027
May 6, 2026
May 1, 2026
4.3 years
February 2, 2022
May 5, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Proportion of correct responses in a forced-choice task after 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
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)
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 Outcomes (5)
Heart rate (bpm)
During the vocal stimuli
Skin conductance (Siemens)
During the vocal stimuli
Skin temperature (°C)
During the vocal stimuli
Nociception Level Index (NOL)
During the vocal stimuli
Pupillary diameter (millimeter)
During the vocal stimuli
Study Arms (1)
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?").
Interventions
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
Eligibility Criteria
Healthy adult population aged 18 to 80 years
You may qualify if:
- \- Participant should be affiliated or entitled to a social security scheme
You may not qualify if:
- Pregnancy
- Hearing impairment, speech production disorders or major health problems.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU Saint-Etienne
Saint-Etienne, 42055, France
Study Officials
- PRINCIPAL INVESTIGATOR
ROLAND PEYRON, MDPHD
CHU DE SAINT-ETIENNE
- STUDY CHAIR
Nicolas MATHEVON, PhD
University of Saint-Etienne, France
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 2, 2022
First Posted
February 23, 2022
Study Start
November 29, 2022
Primary Completion (Estimated)
April 1, 2027
Study Completion (Estimated)
April 1, 2027
Last Updated
May 6, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share