Sensory Profile of People With High Intellectual Potential (HIP)
ConditionHigh Intellectual Potential
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorCentre Hospitalier Esquirol
About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
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)
Gender and Age: Male or female, aged 18 to 65
Disqualifiers
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
Trial 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.
Trial design
Design model
Case-control
Time perspective
Prospective
Treatments tested in this trial
Scales
Other interventionThis 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
Other interventionFor 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.
Treatment groups
160 Participants
are divided into 2 treatment groupsGroup A: High Intellectual Potential2 interventions
Group B: Control1 intervention
Trial outcomes
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.
Time frame
At enrollmentSecondary outcomes
1
Sensory profile from the Adolescent and Adult Sensory Profile according to the cognitive profile of the High Intellectual Potential group.
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.
Time frame
At enrollment2
Scores for anxiety from the State and Trait Anxiety Inventory according to each group
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
Time frame
At enrollment3
Scores for task coping drawn from the Coping Inventory for Stressful Situations according to each group
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.
Time frame
At enrollment4
Description of the frequency of autistic traits for each group
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.
Time frame
At enrollmentSponsors and contacts
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Source ClinicalTrials.gov