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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: |
NCT00728039 |
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Date of registration:
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31/07/2008 |
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Primary sponsor: |
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Public title:
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Quality of Life (QOL), Coping and Psychological Symptoms in Children and Adolescents With Cyclic Vomiting Syndrome
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Scientific title:
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Quality of Life, Coping and Psychological Symptoms in Children and Adolescents With Cyclic Vomiting Syndrome |
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Date of first enrolment:
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April 2007 |
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Target sample size:
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120 |
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Recruitment status: |
Enrolling by invitation |
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URL:
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http://clinicaltrials.gov/show/NCT00728039 |
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Study type:
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Observational |
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Study design:
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Observational Model: Cohort, Time Perspective: Prospective
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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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Sally E Tarbell, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Medical College of Wiconsin |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Diagnosis of CVS
Exclusion Criteria:
- Children and parents who are not English speaking
- Youth with significant developmental delay, mental retardation, psychotic symptoms,
or other significant mental impairments and those with other major medical disorders
such as IDDM, congenital heart disease, cystic fibrosis, etc.
Age minimum:
9 Years
Age maximum:
18 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Vomiting Syndrome
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Primary Outcome(s)
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Characterize the quality of life of youth with CVS as well as the strategies they use to cope with stress, their strengths and vulnerabilities, and to assess symptoms of depression and anxiety in these at risk youth.
[Time Frame: Two years]
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Secondary Outcome(s)
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Evaluate the associations among coping strategies the frequency and intensity of CVS attacks to determine if particular coping styles and personal characteristics are associated illness severity, psychiatric co-morbidity and quality of life.
[Time Frame: Two years]
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Secondary ID(s)
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07/82
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GC 399
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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