Sensory Profile of People With High Intellectual Potential (HIP)
HPIsens
1 other identifier
observational
160
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Apr 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2025
CompletedFirst Submitted
Initial submission to the registry
July 9, 2025
CompletedFirst Posted
Study publicly available on registry
July 18, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
April 1, 2027
July 24, 2025
July 1, 2025
2 years
July 9, 2025
July 21, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Sensory profile from the Adolescent and Adult Sensory Profile according to each group.
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 Outcomes (4)
Sensory profile from the Adolescent and Adult Sensory Profile according to the cognitive profile of the High Intellectual Potential group.
At enrollment
Scores for anxiety from the State and Trait Anxiety Inventory according to each group
At enrollment
Scores for task coping drawn from the Coping Inventory for Stressful Situations according to each group
At enrollment
Description of the frequency of autistic traits for each group
At enrollment
Study Arms (2)
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
Control
Subjects whitout High Intellectual Potential
Interventions
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.
Eligibility Criteria
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.
You may qualify if:
- 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)
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Esquirol Hospital Center
Limoges, Nouvelle-Aquitaine, 87025, France
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Psychomotor Therapist, Doctor in Psychology
Study Record Dates
First Submitted
July 9, 2025
First Posted
July 18, 2025
Study Start
April 1, 2025
Primary Completion (Estimated)
April 1, 2027
Study Completion (Estimated)
April 1, 2027
Last Updated
July 24, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share