- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05520996
Impact of Ostracism on Prospective Memory in ADHD Children With or Without Emotional Dysregulation (IOM-ADHD)
April 28, 2026 updated by: University Hospital, Rouen
Impact of Ostracism on Prospective Memory in ADHD Children With or Without Emotional Dysregulation/ Impact de l'Ostracisme Sur la mémoire Prospective Chez Des Enfants Atteint de TDA/H Avec ou Sans dysrégulation émotionnelle.
Assess the effect of exposure to a situation of social exclusion or ostracism on the prospective memory of children with ADHD
Study Overview
Study Type
Observational
Enrollment (Actual)
24
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
-
-
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Rouen, France, 76031
- CHU - Rouen
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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
8 years to 12 years (Child)
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
Child with attention deficit disorder with or without hyperactivity
Description
Inclusion Criteria:
- Child with attention deficit disorder with or without hyperactivity (ADHD) according to the following criteria: score greater than 27 on the ADHD-RS scale or score greater than 65 on the Conners scale, and after clinical staff discussion
- Social security
- non opposition of parents and children to the study
Exclusion Criteria:
- Subject presenting elements in favor of a depressive disorder according to a clinical evaluation and on an evaluation by the CBCL scale
- Minor and/or parents who do not understand French
- Person under legal protection, adult guardianship or curatorship.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
one arm study
Memory test performed before and after cyberball task
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Social exclusion or ostracism can be measured by the Cyberball 5 task.
The principle of Cyberball is based on the creation of a situation of exclusion through a computerized task.
During this task, the participant passes a ball to 2 other players controlled by Artificial Intelligence (AI).
The ball-passing method of AI-controlled players is determined in advance in the computer program code.
A series of ball passing is carried out with initially an equal passing between the three participants and then an exclusive passing between the players controlled by an artificial intelligence
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
difference between prospective memory tests performed before and after cyberball task
Time Frame: At inlcusion
|
Promacy test is a Memory test performed before and after Cyberball task
|
At inlcusion
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 15, 2021
Primary Completion (Actual)
June 21, 2022
Study Completion (Actual)
June 21, 2022
Study Registration Dates
First Submitted
March 14, 2022
First Submitted That Met QC Criteria
August 26, 2022
First Posted (Actual)
August 30, 2022
Study Record Updates
Last Update Posted (Actual)
May 4, 2026
Last Update Submitted That Met QC Criteria
April 28, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021/0224/OB
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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