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SAMPLEXWorking Memory Training and Individual Neurocognitive Changes Study

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
Study Aim

This study aims to observe how working memory training affects your cognitive abilities, using performance measures from home-based training and a task called Spatial Span from the CANTAB battery, as well as tracking changes in your brain using multimodal MRI data before, during, and after the training phase.

What is being collected

Data Collection

Who is being recruted

Behavior

+ Personal Satisfaction

+ Psychological Well-Being

From 18 to 30 Years
+10 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Case-Only

Examining characteristics of individuals with a disease in order to identify genetic or environmental factors contributing to the condition.
Observational
Study Start: September 2025
See protocol details

Summary

Principal SponsorCentre Hospitalier St Anne
Study ContactCACHIA Arnaud
Last updated: October 1, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 29, 2025

Actual date on which the first participant was enrolled.

The participants will benefit from a comprehensive training program in the Memory of the taught by the computerized CogMed method. This training showed a positive effect for improve the skills in Memory of the working in the healthy subject

Principal SponsorCentre Hospitalier St Anne
Study ContactCACHIA Arnaud
Last updated: October 1, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

8 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-only

These studies focus only on individuals who have a specific disease. Researchers examine patterns—often genetic or environmental—to uncover what might be linked to the condition.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 30 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

BehaviorPersonal SatisfactionPsychological Well-Being

Criteria

5 inclusion criteria required to participate
The inclusion criteria include

age between 18 and 30 years

native French speaker, affiliation with the French national health insurance system

provision of written informed consent prior to participation

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5 exclusion criteria prevent from participating
Exclusion criteria include

any geographical or psychological condition preventing full compliance with the study protocol

contraindications to MRI

history of traumatic brain injury

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Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

CACHIA

Paris, FranceOpen CACHIA in Google Maps
Recruiting
One Study Center