NCT05238285

Brief Summary

Like many other animals, humans produce nonverbal vocal signals including screams, grunts, roars, cries and laughter across a variety of contexts. However, despite their importance in the human vocal repertoire, the mechanisms and functions of non-verbal signals remain little studied and poorly understood in humans.Our studies aim to improve our understanding of the nature and function of non-verbal signals.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,000

participants targeted

Target at P75+ for all trials

Timeline
11mo left

Started Mar 2023

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Progress78%
Mar 2023Apr 2027

First Submitted

Initial submission to the registry

February 2, 2022

Completed
12 days until next milestone

First Posted

Study publicly available on registry

February 14, 2022

Completed
1.1 years until next milestone

Study Start

First participant enrolled

March 8, 2023

Completed
4.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2027

Last Updated

May 6, 2026

Status Verified

May 1, 2026

Enrollment Period

4.1 years

First QC Date

February 2, 2022

Last Update Submit

May 5, 2026

Conditions

Keywords

acoustic analysisphysiological responsespsycho-acoustic tests

Outcome Measures

Primary Outcomes (1)

  • Vocal analysis

    Participants will receive instructions on what to say or what type of non-verbal vocalisation to produce during the manipulation. The vocalisations thus produced by the participants will be systematically recorded and analysed using software adapted to acoustic analysis Measurement of acoustic variables such as fundamental frequency (pitch), vocal tract resonances (formants) and vocal disturbances (jitter, shimmer), the nonlinearities and chaotic/noise properties of vocalisations

    During the vocal production

Secondary Outcomes (5)

  • Heart rate (bpm)

    During the vocal production

  • Skin conductance (Siemens)

    During the vocal production

  • Skin temperature (°C)

    During the vocal production

  • Nociception Level Index (NOL)

    During the vocal production

  • Pupillary diameter (millimeter)

    During the vocal production

Study Arms (1)

Healthy adult population aged 18 to 80 years

Participants will be asked to produce vocal sounds of different nature according to the non-verbal parameters of interest for the given study.

Behavioral: Production of vocal sounds

Interventions

Participants will be asked to produce vocal sounds of different nature according to the non-verbal parameters of interest for the given study. For example, they can read a script containing vowels ('a', 'e', 'i', 'o', 'u'), short sentences ('hello, how are you'), longer passages of standardised reading texts, and can also be asked to speak freely about any topic ('freedom of speech'). They can be asked to play a role or to imitate a particular emotional state. For example, "imagine that you have just been told that you have won a million euros in the lottery. Produce a vocalisation to express your excitement" or "talk to your dog your dog by imagining that he has done a negative action and then do the same thing by imagining that this time imagining that the action was positive".

Healthy adult population aged 18 to 80 years

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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:

  • Pregnant women
  • Voice production disorders
  • Hearing impairment, speech production disorders or major health problems.
  • Chronic smoker (more than 10 cigarettes per day)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre Hospitalier Universitaire de Saint-Etienne

Saint-Etienne, 42055, France

RECRUITING

Study Officials

  • ROLAND PEYRON, MDPHD

    Centre Hospitalier Universitaire de Saint Etienne

    PRINCIPAL INVESTIGATOR
  • Nicolas MATHEVON, PhD

    University of Saint-Etienne, France

    STUDY DIRECTOR

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 14, 2022

Study Start

March 8, 2023

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

Locations