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Recruiting NCT07072455

Sensory Profile of People With High Intellectual Potential (HIP)

— Observational High Intellectual Potential

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Scales, High Intellectual Potential Scale.
Who it may be relevant to
Registry conditions: High Intellectual Potential. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Sensory Profile of People With High Intellectual Potential

Overview

This is a prospective observational psychology study on a non-clinical population, involving the use of questionnaires (non-interventional research). This study involves the collection of data associated with High Intellectual Potential characteristics, sensory profile, and includes clinical measures such as anxiety anxiety, autistic traits and coping in High Intellectual Potential and control participants.

Interventions

  • Other Scales
    This observational study consists of data collection using a structured questionnaire based on an e-CRF, distributed by e-mail. Four questionnaires were administered : the Revised Ritvo Autism and Asperger Diagnostic Scale (RAADS-R-Fr), the Adolescent/Adult Sensory Profile (AASP), the Coping Inventory for Stressful Situations (CISS) and the State-Trait Anxiety Inventory (STAI-Y). Socio-demographic and treatments were collected.
  • Other High Intellectual Potential Scale
    For participants with High Intellectual Potential, the total Intelligence Quotient (IQ) or General Ability Index (GAI), along with the index scores from the Wechsler scales (Verbal Comprehension Index, Perceptual Reasoning Index, Working Memory Index, and Processing Speed Index), will be extracted from the cognitive assessment previously completed by the participant prior to study enrollment.

Primary outcome measures

  • Sensory profile from the Adolescent and Adult Sensory Profile according to each group. [Time frame: At enrollment]
Secondary outcome measures (4)
  • Sensory profile from the Adolescent and Adult Sensory Profile according to the cognitive profile of the High Intellectual Potential group. [Time frame: At enrollment]
  • Scores for anxiety from the State and Trait Anxiety Inventory according to each group [Time frame: At enrollment]
  • Scores for task coping drawn from the Coping Inventory for Stressful Situations according to each group [Time frame: At enrollment]
  • Description of the frequency of autistic traits for each group [Time frame: At enrollment]

Eligibility criteria

Inclusion criteria

  • High Intellectual Potential:
  • Participants with a High Intellectual Potential : Cognitive assessment using the WAIS or WISC-V scale by a psychologist; Intelligence Quotient (IQ) ≥ 130, in the case of a homogeneous cognitive profile, or General Aptitude Index (GAI) > 130 \[124-134\], in the case of a heterogeneous cognitive profile
  • Gender and Age: Male or female, aged 18 to 65
  • Consent: Free, informed, and written consent (e-CRF)
  • Control :
  • Gender and Age: Male or female, aged 18 to 65
  • Consent: Free, informed, and written consent (e-CRF)

Exclusion criteria

  • High Intellectual Potential:
  • History or declared psychiatric disorder (characterized depressive episode, personality disorder, addiction, eating disorder, bipolar disorder, obsessive-compulsive disorder)
  • Neurodevelopmental disorders (autism spectrum disorder, attention deficit and hyperactivity disorder , developmental coordination disorder)
  • Sensory disability
  • Subjects under guardianship or curatorship
  • Pregnant or breast-feeding women
  • Control :
  • Presence of High Intellectual Potential known
  • Presence of intellectual development disorder
  • History or declared psychiatric disorder (characterized depressive episode, personality disorder, addiction, eating disorder, bipolar disorder, obsessive-compulsive disorder)
  • Neurodevelopmental disorders (autism spectrum disorder, attention deficit and hyperactivity disorder , developmental coordination disorder)
  • Sensory disability
  • Subjects under guardianship or curatorship
  • Pregnant or breast-feeding women

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-control

Study locations

France · 1 center
  • Esquirol Hospital Center — Limoges

Identifiers

NCT: NCT07072455 · 2024-A02488-39

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗