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Main
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Note: This record shows only 22 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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22 August 2016 |
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Main ID: |
NCT01990131 |
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Date of registration:
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15/11/2013 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Computerized Anxiety Treatment for Suicide
CATS |
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Scientific title:
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Suicide Risk Prevention Among Patients With Anxiety Psychopathology |
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Date of first enrolment:
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October 2013 |
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Target sample size:
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74 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT01990131 |
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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: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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United States
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Meet diagnostic criteria for a primary Axis 1 anxiety disorder or meet diagnostic
criteria for a unipolar mood disorder along with an Axis 1 anxiety disorder.
- Show evidence of current suicidal ideation (BSS above 6.
- Show elevated AS indicated by scoring at or above the community sample mean on the
ASI-Cog (above 9.
Exclusion Criteria:
- No significant medical illness (e.g. sig cardiovascular disease, epilepsy, stroke).
- Current or past psychotic-spectrum disorders or uncontrolled bipolar disorder
- No current substance dependence
- Must be an English speaker.
- Must be 18 years or older.
- Must have normal or corrected vision
- Cannot begin treatment/therapy within 1 month of baseline.
- Cannot begin a new medication within 3 months of baseline.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Suicide
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Anxiety
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Intervention(s)
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Other: Cognitive Anxiety Sensitivity Treatment
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Other: Physical Health Education Training
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Primary Outcome(s)
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Anxiety Sensitivity Index-3 (ASI-3)
[Time Frame: Month 4 follow-up]
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Secondary Outcome(s)
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Beck Suicide Scale (BSS)
[Time Frame: Month 4 follow-up]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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