NCT07072455

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
160

participants targeted

Target at P50-P75 for all trials

Timeline
11mo left

Started Apr 2025

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress55%
Apr 2025Apr 2027

Study Start

First participant enrolled

April 1, 2025

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

July 9, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

July 18, 2025

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2027

Last Updated

July 24, 2025

Status Verified

July 1, 2025

Enrollment Period

2 years

First QC Date

July 9, 2025

Last Update Submit

July 21, 2025

Conditions

Keywords

High Intellectual PotentialSensory ProfileCoping StrategiesAnxietySensory ProcessingAutistic traits

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

Other: ScalesOther: High Intellectual Potential Scale

Control

Subjects whitout High Intellectual Potential

Other: Scales

Interventions

ScalesOTHER

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.

ControlHigh Intellectual Potential

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.

High Intellectual Potential

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-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.

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

RECRUITING

MeSH Terms

Conditions

Anxiety Disorders

Interventions

Weights and Measures

Condition Hierarchy (Ancestors)

Mental Disorders

Intervention Hierarchy (Ancestors)

Investigative Techniques

Central Study Contacts

Aude Paquet, PhD in Psychology

CONTACT

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

Locations