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Clinical Trial Details — Status: Unknown status

Administrative data

NCT number NCT01031511
Other study ID # DSRB Ref Code: A/05/091
Secondary ID NMRC/1002/200513
Status Unknown status
Phase Early Phase 1
First received December 11, 2009
Last updated December 11, 2009
Start date June 2005
Est. completion date February 2011

Study information

Verified date February 2009
Source National Healthcare Group, Singapore
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Cognitive Behavioural Therapy is an effective intervention program for children with High-Functioning Autistic Spectrum Disorder to remediate anxiety issues.


Recruitment information / eligibility

Status Unknown status
Enrollment 73
Est. completion date February 2011
Est. primary completion date January 2010
Accepts healthy volunteers No
Gender All
Age group 9 Years to 16 Years
Eligibility Inclusion Criteria:

- Assessed to have Autistic Spectrum Disorder, Asperger Syndrome, Pervasive Developmental Disorder, Not Otherwise Specified by the DSM-IV criteria, based on clinical interview, Asperger Syndrome Diagnostic Scale (ASDS) or Autism Diagnostic Observation Schedule (ADOS)

- Child have a Verbal Comprehension Index of 80 and Perceptual Reasoning Index of 90 and above

- No change of medication dosage 1 month prior to the commencement of program for the child and through out the duration of the study

- Written parental consent and assent from children above 12 years old

Exclusion Criteria:

- Children with Verbal Comprehension Index of 80 and Perceptual Reasoning Index of 90 and below.

- Children who are undergoing other Cognitive Behavioural treatment program concurrently

- Those without parental consent will not be able to participate

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Cognitive Behavioural Therapy
16 weekly sessions of 1.5 hrs in small groups of 3-4 children conducted by 2 therapists
Other:
Social Recreational
16 weekly sessions of 1.5 hrs in small groups of 3-4 children, conducted by 2 therapists

Locations

Country Name City State
Singapore Institute of Mental Health, Singapore Singapore

Sponsors (3)

Lead Sponsor Collaborator
National Healthcare Group, Singapore Autism Resource Centre, Singapore, Nanyang Technological University

Country where clinical trial is conducted

Singapore, 

Outcome

Type Measure Description Time frame Safety issue
Primary Anxiety level of child Pre Treatment, Post-treatment, 3 months follow-up, 6 months follow-up, One year follow-up
Secondary Parent Stress Level Pre Treatment, Post-treatment, 3 months follow-up, 6 months follow-up, One year follow-up
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