Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
All Genders
ID04025398

REHABILITUS: A New Cognitive Remediation Tool for Adults With Intellectual Disability and Behavioral Disorders

Led by Hôpital le Vinatier · Updated on 2025-07-31

116

Participants Needed

1

Research Sites

28 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Adults with intellectual disabilities often face challenges in social situations due to difficulties in processing social information, especially in recognizing facial emotions. This research evaluates a cognitive remediation program called Re9habilitus, designed to improve attentional and visuospatial functions to reduce behavioral disorders in adults with intellectual disabilities who do not have autism spectrum disorder. The study aims to validate whether this program can help address specific cognitive and behavioral issues in daily life for this population. Participants are randomly assigned to either the Re9habilitus cognitive remediation program, which focuses on improving attention and spatial perception related to social behavior, or to a control group engaging in manual activities and computer-based research tasks. The study compares these two approaches to assess their effects on behavioral disorders and cognitive functions. During the study, participants are assessed on changes in hyperactivity and non-compliance behaviors using the Aberrant Behavior Checklist scale over six months. Researchers also measure improvements in facial emotion recognition and attentional functions at the start, end, and six months after the intervention. The total participation time and safety monitoring details are aligned with the evaluation periods, ensuring thorough follow-up to observe lasting effects.

CONDITIONS

Brief Title

A Computer-based Cognitive Remediation Program for Adults With Intellectual Disability

Who Can Participate

Age: 18Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 45 inclusive
  • Behavioral disorders with a total score on the Aberrant Behavior Checklist above 15
  • Presence of a family caregiver or professional involved in the project
  • Diagnosis of mild to moderate intellectual disability assessed within the last 3 years
  • French as primary or secondary language
  • Psychoactive treatment unchanged during the month before inclusion
  • Adult or legal representative has given written informed consent
  • Affiliated with or beneficiary of a social security scheme
Not Eligible

You will not qualify if you...

  • Neurological disorders of vascular, infectious, or neurodegenerative origin
  • Taking medications with neurological or psychiatric impact (e.g., corticosteroids)
  • Participation in another cognitive remediation program targeting attention, visuospatial, or social cognition
  • Refusal of participation by the person or legal representative
  • Absence of a family or professional caregiver
  • Presence of Autistic Spectrum Disorders evaluated if necessary

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 months

Participants receive either the Réhabilitus cognitive remediation program focusing on attention and visuospatial functions or participate in manual activities and research computer information as part of the control group.

Weekly visits during the intervention period

Follow-up

Duration - 6 months

Participants are assessed to investigate the possible long-lasting effects of the intervention on behavioral disorders and cognitive functions.

1 visit at the end of the follow-up period

Trial Site Locations

Total: 1 location

1

Hopital Vinatier

Lyon, Auvergne-Rhône-Alpes, France, 69678

Actively Recruiting

Loading map...

Research Team

D

DEMILY CAROLINE, MD Ph

B

BABINET MARIE-NOELLE

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Similar Trials

Evaluation of Bladder and Bowel Functions, Participation and...

Intellectual Disability

Actively Recruiting

1 location

Characterization of the Nociception Phenotype in Individuals...

Intellectual Disability

Actively Recruiting

1 location

Safety, Tolerability and Preliminary Efficacy Study of a Sin...

Developmental Delay Disorder

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here