Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
All Genders
Healthy Volunteers
NCT07303270

Emotional Processes in Adults With Intellectual Developmental Disorder

Led by Hôpital le Vinatier · Updated on 2026-04-01

60

Participants Needed

1

Research Sites

143 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Emotions play a crucial part in the quality of life, interpersonal relationships and mental health in general. In adults presenting with intellectual developmental disorder (IDD), emotional abilities may be hindered, thus leading to more challenging behaviors. A better understanding of emotional processes of adults with IDD may help improve the efficiency of behavioral interventions and better improve their quality of life. The primary goal of this study is to better characterize the abilities and weaknesses of adults with IDD concerning their emotional processes, in comparison to a healthy population. The secondary goals are : * to determine if these difficulties are underlined by oculomotor and attention (auditory and visual) processes * to determine if behavioral difficulties, as reported by the families of adults with IDD, are underlined by specific difficulties in facial emotion recognition, emotion identification in context and/or identification of vocal emotions.

CONDITIONS

Official Title

Emotional Processes in Adults With Intellectual Developmental Disorder

Who Can Participate

Age: 18Years - 35Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of IDD according to DSM-V criteria (IDD group)
  • Aged between 18 and 35 years (both groups)
  • French speaking (both groups)
  • Membership or entitlement to a social security plan (both groups)
  • Informed consent (or from tutor for IDD group) to take part in the study
  • Presence of a caregiver to complete questionnaires at visit 2 (IDD group)
Not Eligible

You will not qualify if you...

  • Visual or auditory impairments evaluated at visit 1 (both groups)
  • Non-stabilized epilepsy (both groups)
  • Treatments impacting brain or psychological functioning (both groups)
  • Major motor disorders (both groups)
  • Breastfeeding or pregnant women (both groups)
  • Neurodevelopmental or psychiatric disorder (control group)
  • History of brain trauma or non-stabilized epilepsy (control group)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CH Le Vinatier

Bron, France, 69500

Actively Recruiting

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Research Team

M

Marie-Noelle Babinet, PhD

CONTACT

M

Méline Devaluez, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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