- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02851836
Attachment Image Data Set Validation in Adolescent (MONRADO1)
July 28, 2016 updated by: Centre Hospitalier Universitaire de Besancon
Validation of an Attachment Picture Set in School-adolescent
this study aims to validate a picture data set that particularly activates the attachment process and that could be used in attachment studies.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Pictures have been chosen to represent several emotions: distress, comfort, complicity and neutral.
Study Type
Interventional
Enrollment (Actual)
133
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
-
-
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 18 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- adolescent going to high school not hospitalized
Exclusion Criteria:
- mental retardation non comprehension of french visual deficit
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
- 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 |
---|---|---|
mean score of valence in the SAM (self assessment manikin system)
Time Frame: at inclusion
|
the hedonicity is assessed for each picture.
The characterization of the set is performed using the mean score of hedonicity for each type of picture (distress, comfort, complicity and neural)
|
at inclusion
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
mean score of arousal in the SAM (self assessment manikin system)
Time Frame: at inclusion
|
the hedonicity is assessed for each picture.
The characterization of the set is performed using the mean score of arousal for each type of picture (distress, comfort, complicity and neural)
|
at inclusion
|
mean score of dominance in the SAM (self assessment manikin system)
Time Frame: at inclusion
|
the hedonicity is assessed for each picture.
The characterization of the set is performed using the mean score of dominance for each type of picture (distress, comfort, complicity and neural)
|
at inclusion
|
emotional categorization of the picture
Time Frame: at inclusion
|
continuous scales for different emotions (distress, comfort, joy-complicity hate, horror) are presented.
Subjects have to quote them for each picture.
|
at inclusion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Lauriane Vulliez-Coady, MD PhD, Centre Hospitalier Universitaire de Besancon
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.
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
October 1, 2012
Primary Completion (Actual)
May 1, 2013
Study Completion (Actual)
November 1, 2013
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 (Estimate)
August 2, 2016
Last Update Submitted That Met QC Criteria
July 28, 2016
Last Verified
July 1, 2016
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- P/2012/152
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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