NCT04533126

Brief Summary

Communication is a social process involving individuals exchanging messages. It is usual to observe different reactions according to the manner of communication, the manner in which such information is exchanged. In this work, it will be examined how different communication modalities cause different reactions in a person. We make the assumption that each communication modality is based on a different brain network.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Sep 2020

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 27, 2020

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 31, 2020

Completed
15 days until next milestone

Study Start

First participant enrolled

September 15, 2020

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2021

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2021

Completed
Last Updated

November 4, 2020

Status Verified

October 1, 2020

Enrollment Period

12 months

First QC Date

August 27, 2020

Last Update Submit

November 3, 2020

Conditions

Keywords

Communication channelPersonalityBrain networkfMRIProcess communication model

Outcome Measures

Primary Outcomes (1)

  • Changes in fMRI activity level

    Measure the differences in fMRI BOLD activation in healthy subjects while viewing typical videos of four different types of communication channels.

    1-day

Eligibility Criteria

Age20 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Healthy participants, medical students

You may qualify if:

  • Healthy volunteers.
  • Both sexes (1:1).
  • Aged between 20 and 30 years old.
  • Medical student, from L2.
  • A person who has signed a written, free and informed consent.
  • Person affiliated to a social security scheme.

You may not qualify if:

  • Current clinically significant psychiatric disorder (MINI 7.0): mood disorder, bipolar disorder, psychotic disorder, substance abuse.
  • Current or past neurological disorder with current functional impact.
  • Chronic unstable somatic pathology.
  • Occasional use of medication other than contraceptives, migraine medication, or analgesics.
  • MRI contraindications, including claustrophobia.
  • Pregnant or breastfeeding woman.
  • Subject deprived of liberty (by a judicial or administrative decision).
  • Subject protected by law (subject under guardianship and curatorship).
  • Legal incapacity and/or other circumstances rendering the subject incapable of understanding the nature, purpose or consequences of the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre Investigation Clinique

Tours, Centre-Val de Loire, 37044, France

RECRUITING

MeSH Terms

Conditions

Communication

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • GISSOT Valérie, MD

    CHRU Tours - CIC1415

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 27, 2020

First Posted

August 31, 2020

Study Start

September 15, 2020

Primary Completion

September 1, 2021

Study Completion

December 1, 2021

Last Updated

November 4, 2020

Record last verified: 2020-10

Data Sharing

IPD Sharing
Will not share

Locations