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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02851810
Other study ID # API/2012/35
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 19, 2013
Est. completion date June 8, 2017

Study information

Verified date October 2018
Source Centre Hospitalier Universitaire de Besancon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Completed
Enrollment 124
Est. completion date June 8, 2017
Est. primary completion date June 8, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 13 Years to 20 Years
Eligibility Inclusion Criteria:

- non hospitalized child who is going to school

Exclusion Criteria:

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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
oculomotor parameter recording
visual scanning behavior is assessed during visualization of emotional pictures
attachment scale interview (ASI)
ASI is used to determine the attachment style of each participant
psychophysiological recording
this consists of the measurement of the skin conductance reactivity (SCR) during the picture visualization
psychometric assessment
self administered questionnaires are used to assess anxiety, depression and alexithymia.
parent interview
an interview of the adolescent parent is performed in order to assess the confusion of the parent-child role and the interaction between the child and its parent.

Locations

Country Name City State
France CHU Besancon Besancon Doubs

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Besancon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of entry in distress pictures these parameters will be compared between the different types of attachment. within 1 year after inclusion
Primary saccade duration in distress picture time spent looking at the distress picture these parameters will be compared between the different types of attachment. within 1 year after inclusion
Primary average of the number of entry in comfort picture vs neutral and complicity pictures these parameters will be compared between the different types of attachment. within 1 year after inclusion
Primary average of the saccade duration in comfort picture vs neutral and complicity pictures these parameters will be compared between the different types of attachment. within 1 year after inclusion
Secondary Amplitude of SCR this parameter will be compared between the different types of attachment. within 1 year after inclusion
Secondary interaction with the parent: score to the GPACS (goal-corrected partnership in adolescence coding system) 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
Secondary Reaction time in SCR this parameter will be compared between the different types of attachment. within 1 year after inclusion
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