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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT00164554 |
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Date of registration:
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12/09/2005 |
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Primary sponsor: |
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Public title:
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Fetal Alcohol Syndrome/ARND Research Consortion
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Scientific title:
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Fetal Alcohol Syndrome/ARND Research Consortion-Oklahoma |
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Date of first enrolment:
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October 2001 |
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Target sample size:
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100 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT00164554 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind
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Countries of recruitment
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United States
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Contacts
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Name:
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John Mulvihill, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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University of Oklahoma |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Children ages 3 to 7 years
Age minimum:
3 Years
Age maximum:
7 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Fetal Alcohol Syndrome
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Intervention(s)
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Behavioral: Parent-child Interaction Therapy (PCIT)
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Primary Outcome(s)
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compliance with directives
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Secondary ID(s)
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CDC-NCBDDD-3813
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U84/CCU020163-02
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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