Oculomotor Markers and Attachment in Adolescents (MONRADO2)

October 1, 2018 updated by: Centre Hospitalier Universitaire de Besancon

Oculomotor and Neurophysiological Markers of Emotion Regulation and Attachment Styles in Adolescence

The study aims to identify specific visual scanning patterns of attachment pictures in adolescent with different attachment style.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Oculomotor parameters will be assessed during visualization of 2 sets of pictures. The first set presents a distress picture and is followed by a slide composed of 3 pictures (one representing comfort, one representing complicity and the last representing a neutral scene).

Psychophysiological parameters (skin conductance reactivity-SCR) is also assess during this visualization.

Study Type

Interventional

Enrollment (Actual)

124

Phase

  • Not Applicable

Contacts and Locations

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

Study Locations

  • France
    • Doubs
      • Besancon, Doubs, France, 25030
        • CHU Besançon

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

13 years to 20 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • non hospitalized child who is going to school

Exclusion Criteria:

  • not french-speaker vision problem more than 20 cigarettes/day

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

  • Primary Purpose: Basic Science
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
number of entry in distress pictures
Time Frame: within 1 year after inclusion
these parameters will be compared between the different types of attachment.
within 1 year after inclusion
saccade duration in distress picture
Time Frame: within 1 year after inclusion
time spent looking at the distress picture these parameters will be compared between the different types of attachment.
within 1 year after inclusion
average of the number of entry in comfort picture vs neutral and complicity pictures
Time Frame: within 1 year after inclusion
these parameters will be compared between the different types of attachment.
within 1 year after inclusion
average of the saccade duration in comfort picture vs neutral and complicity pictures
Time Frame: within 1 year after inclusion
these parameters will be compared between the different types of attachment.
within 1 year after inclusion

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Amplitude of SCR
Time Frame: within 1 year after inclusion
this parameter will be compared between the different types of attachment.
within 1 year after inclusion
interaction with the parent: score to the GPACS (goal-corrected partnership in adolescence coding system)
Time Frame: within 1 year after inclusion
the quality of the interaction with the parent and the confusion of the parent-child role will be compared between the different attachment types.
within 1 year after inclusion
Reaction time in SCR
Time Frame: within 1 year after inclusion
this parameter will be compared between the different types of attachment.
within 1 year after inclusion

Collaborators and Investigators

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

Sponsor

Centre Hospitalier Universitaire de Besancon

Investigators

  • Principal Investigator: Lauriane Vulliez-Coady, MD PhD, Centre Hospitalier Universitaire de Besançon

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

December 19, 2013

Primary Completion (Actual)

June 8, 2017

Study Completion (Actual)

June 8, 2017

Study Registration Dates

First Submitted

July 26, 2016

First Submitted That Met QC Criteria

July 28, 2016

First Posted (Estimate)

August 2, 2016

Study Record Updates

Last Update Posted (Actual)

October 2, 2018

Last Update Submitted That Met QC Criteria

October 1, 2018

Last Verified

October 1, 2018

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • API/2012/35

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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