Sensory Profile of People With High Intellectual Potential (HIP) (HPIsens)

July 21, 2025 updated by: Aude Paquet, Centre Hospitalier Esquirol

Sensory Profile of People With High Intellectual Potential

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.

Study Overview

Study Type

Observational

Enrollment (Estimated)

160

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Nouvelle-Aquitaine
      • Limoges, Nouvelle-Aquitaine, France, 87025
        • Recruiting
        • Esquirol Hospital Center
        • Contact:
        • Principal Investigator:
          • Aude Paquet, PhD in Psychology

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Subjects with High Intellectual Potential will be recruited on a voluntary basis :

  • in the offices of private psychologists, on the psychologist's recommendation or by posting in waiting rooms
  • through communication on social networks Subjects control will be recruited on a voluntary basis from the personal and professional environment of the people involved in this study and through communication on social networks.

Description

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

Study Plan

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

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
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

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.

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

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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sensory profile from the Adolescent and Adult Sensory Profile according to each group.
Time Frame: At enrollment
Sensory profile scores is obtained using the self-report questionnaire Adolescent and Adult Sensory Profile (AASP) after the participant has been included in the study. Subscores for sensory sensitivity, low registration, sensation seeking, and sensation avoidance are collected. For each subscore, the minimum and maximum values range from 15 to 75. A high score indicates high sensory sensitivity.
At enrollment

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Description of the frequency of autistic traits for each group
Time Frame: At enrollment
The frequency of autistic traits will be obtained using the Revised Ritvo Autism and Asperger Diagnostic Scale (RAADS-R-Fr) during an individual interview after the participant has been included in the study. The minimum and maximum values range from 0 to 240. The generally accepted threshold for significant autistic traits is 70. A high score indicate high autistic traits.
At enrollment
Sensory profile from the Adolescent and Adult Sensory Profile according to the cognitive profile of the High Intellectual Potential group.
Time Frame: At enrollment
Sensory profile scores will be obtained using the Adolescent and Adult Sensory Profile (AASP) scale during an individual interview after the participant has been included in the study. Subscores for sensory sensitivity, low registration, sensation seeking, and sensation avoidance will be collected. For each subscore, the minimum and maximum values range from 15 to 75. A high score indicates high sensory sensitivity.
At enrollment
Scores for anxiety from the State and Trait Anxiety Inventory according to each group
Time Frame: At enrollment
Anxiety scores will be obtained using the State and Trait Anxiety Inventory (STAI-Y) scale during an individual interview after the participant has been included in the study. Subscores for State Anxiety and Trait Anxiety will be collected. For each subscore, the minimum and maximum values range from 20 to 80. A high score indicates high anxiety
At enrollment
Scores for task coping drawn from the Coping Inventory for Stressful Situations according to each group
Time Frame: At enrollment
Coping scores will be obtained using the Coping Inventory for Stressful Situations (CISS) scale during an individual interview after the participant has been included in the study. The task-oriented coping subscore, emotion subscore, avoidance subscore, distraction subscore, and social diversion subscore will be collected. The minimum and maximum values range from 16 to 90. A high score indicates high oriented coping.
At enrollment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2025

Primary Completion (Estimated)

April 1, 2027

Study Completion (Estimated)

April 1, 2027

Study Registration Dates

First Submitted

July 9, 2025

First Submitted That Met QC Criteria

July 9, 2025

First Posted (Actual)

July 18, 2025

Study Record Updates

Last Update Posted (Actual)

July 24, 2025

Last Update Submitted That Met QC Criteria

July 21, 2025

Last Verified

July 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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