Sensory Profile of People With High Intellectual Potential (HIP)

NCT ID: NCT07072455

Last Updated: 2025-07-24

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 160 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2025-04-01
• Study Completion Date: 2027-04-30

Brief Summary

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.

Conditions

High Intellectual Potential

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Study Groups

High Intellectual Potential

Subjects with a High Intellectual Potential : Cognitive assessment using the Wechsler Adult Intelligence Scale (WAIS-III or WAIS-IV) scale or Wechsler Intelligence Scale for Children (WISC-VI 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

Scales

Intervention Type: OTHER

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.

High Intellectual Potential Scale

Intervention Type: OTHER

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.

Control

Subjects whitout High Intellectual Potential

Scales

Intervention Type: OTHER

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.

Interventions

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.

Intervention Type: 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.

Intervention Type: OTHER

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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Centre Hospitalier Esquirol

OTHER

Sponsor Role: lead

Responsible Party

Aude Paquet

Psychomotor Therapist, Doctor in Psychology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Esquirol Hospital Center

Limoges, Nouvelle-Aquitaine, France

Site Status: RECRUITING

Countries

France

Central Contacts

Aude Paquet, PhD in Psychology

Role: CONTACT

aude.paquet@ch-esquirol-limoges.fr

+33 5-55-43-11-27

Facility Contacts

Alexandra Foucher, University degree

Role: primary

alexandra.foucher@ch-esquirol-limoges.fr

+33 5-55-43-11-00

Other Identifiers

2024-A02488-39

Identifier Type: -

Identifier Source: org_study_id