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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00505830
Other study ID # Autisme AQ
Secondary ID
Status Recruiting
Phase N/A
First received July 23, 2007
Last updated July 23, 2007
Start date July 2007
Est. completion date July 2009

Study information

Verified date July 2007
Source Groupe Francais d'Epidemiologie Psychiatrique
Contact Jean-Pierre Vignat, MDH
Phone +33 4 37 90 11 75
Email jpvignat@ch-st-jean-de-dieu-lyon.fr
Is FDA regulated No
Health authority France: Ministry of Health
Study type Observational

Clinical Trial Summary

Autism is considered as an invading disorder of the development. Asperger Syndrome (AS) is a particular form of autism and is difficult to diagnose. The Autism Spectrum Quotient (AQ) has been developed in order to measure the degree of autistic traits in autistic adolescent with normal intelligence (Baron-Cohen et al. 2001, 2006). AQ comprises 50 questions, with 5 groups of 10 questions assessing imagination, social skills, attention switching, attention to detail and communication skills. Each of these items scores 1 point if the respondent records abnormal or autistic like behaviour. The minimum score on the AQ is 0 and the maximum 50.

The principal objective of this study is to evaluate the accuracy of the French version of Autism Spectrum Quotient questionnaire.

Secondary objectives are to:

Evaluate if EQ and SQ can distinguish adolescents without psychiatric syndromes from those with classical autism or AS.

Evaluate if AQ, EQ and SQ can distinguish adolescents with psychiatric disorders from autistic adolescents.

Define the threshold of positivity for the 3 questionnaires.


Description:

4 groups of participants will be screened with the questionnaires: Group 1: 50 adolescents with AS or high functioning autism (HFS) diagnosed by psychiatrists using established criteria and with an IQ >85.

Group 2: 50 adolescents with AS or classical autism diagnosed by psychiatrists using established criteria 70
Group 3: 50 adolescents with psychiatric disorders. Group 4: Sample of 50 healthy adolescents selected randomly from 200. The questionnaires are given to the parents of adolescents during the first meeting. Parents are invited to send them back to the clinical investigation centre of Lyon (France).

Multicentre study: 8 clinical centres and 18 paediatricians


Recruitment information / eligibility

Status Recruiting
Enrollment 450
Est. completion date July 2009
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 12 Years to 18 Years
Eligibility Inclusion Criteria:

Group 1 (AS/HFA) and 2 (AS/classic autism) :

- Boys and girls aged 12 to 18

- Patients with autism or Asperger syndrome according to the diagnostic criteria (ICD 10)

- Patients receiving education in an ordinary school

- IQ>70

Group 3 (adolescents with psychiatric disorders):

- Boys and girls aged 12 to 18

- Patients hospitalized on a psychiatric ward or at a psychiatrics patient visit or psychiatric consultation wit hout autistic syndrome

- Patients receiving education in an ordinary school when not in hospital

Group 4 (adolescent without psychiatric syndrome):

- Boys and girls aged 12 to 18

- Patients receiving education in an ordinary school

Exclusion Criteria:

For all groups :

- Problem with language or comprehension

- Participants who have not given their consent

Study Design

Observational Model: Defined Population, Primary Purpose: Screening, Time Perspective: Longitudinal


Related Conditions & MeSH terms


Intervention

Other:
questionnaires
Primary outcome: Autism Spectrum Quotient (AQ) Secondary outcome measure: Empathy quotient (EQ) Systemizing quotient (SQ) WISC III or WISC IV ADOS score ADI score

Locations

Country Name City State
France Centre Hospitalier Saint Jean de Dieu Lyon

Sponsors (2)

Lead Sponsor Collaborator
Groupe Francais d'Epidemiologie Psychiatrique Joint Clinical Research Center

Country where clinical trial is conducted

France, 

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