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Study of ADHD Children's Sensitivity to Memory Error Production (TDAH-DRM)

U

University Hospital, Angers

Status

Completed

Conditions

ADHD

Treatments

Other: DRM (Deese, Roediger et McDermott task)

Study type

Interventional

Funder types

Other

Identifiers

NCT05365295
49RC22-0095

Details and patient eligibility

About

The purpose of the study is to test whether children with Attention Deficit/Hyperactivity Disorder (ADHD) are more susceptible to false memory production using a DRM paradigm. The number of "critical decoy production" errors will be analyzed and compared to the calibration of the test.

Full description

During a neuropsychological assessment, as part of the clinical routine, children with a diagnosis of ADHD, without neurological etiology, aged 8 to 10 years will be offered an additional task. This task, a DRM adapted to the child, consists of learning several lists of words. Each list exposes words belonging to the same lexical field, to a concept not explicitly mentioned in the list, called critical lure. Immediately after the presentation of a list, the child is asked to recall as many words as possible. Recall of the critical lure gives an indication of the production of false memories. The number of critical lures produced by these children will be compared to the calibration of the test, currently being published. The investigator will also verify if the production of critical lures can be correlated with other variables such as performance on intellectual, executive and attentional tasks, proposed during the clinical routine assessment.

The investigator hypothesize that ADHD children will recall more critical lures than the norm, and fewer correct responses than the norm.

The data collected is taken from the child's psychological file. The only personal information used, beyond test performance, is the child's gender and age. The procedure is anonymous.

Enrollment

28 patients

Sex

All

Ages

8 to 11 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age between 96 and 131 months
  • Child referred by a doctor for a neuropsychological assessment
  • Child with ADHD diagnosis
  • Sufficient command of the French language
  • Non-opposition of the child and his/her parents

Exclusion criteria

  • Severe psychiatric comorbidity: major depressive episode, bipolar disorder, generalized anxiety disorder, autism spectrum disorder
  • Major neurological history: severe head trauma, stroke, severe epilepsy, brain tumor
  • Repeating a class during school
  • Presence of an intellectual disability
  • Use of methylphenidate treatment less than 48 hours before the experiment
  • Completion of an intellectual assessment using the Wechsler Intelligence Scale for Children (WISC-V) dated less than one year before the meeting

Trial design

Primary purpose

Screening

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

28 participants in 1 patient group

ADHD
Experimental group
Description:
\- ADHD children aged between 8 to 10 years old
Treatment:
Other: DRM (Deese, Roediger et McDermott task)

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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