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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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12 December 2020 |
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Main ID: |
NCT02309060 |
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Date of registration:
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03/12/2014 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Storytelling Video Intervention for Depressed Primary Care Patients - Open Trial
sTVi-Open |
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Scientific title:
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Narrative Intervention to Disseminate ACT for Depression in Primary Care |
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Date of first enrolment:
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September 2016 |
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Target sample size:
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11 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02309060 |
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Study type:
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Interventional |
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Study design:
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Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Treatment. Masking: None (Open Label).
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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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Contacts
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Name:
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Brandon Gaudiano, 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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Butler Hospital/Brown University |
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Name:
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Lisa Uebelacker, 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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Butler Hospital/Brown University |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
1. Meets DSM-5 criteria for current or lifetime major depressive disorder.
2. No Lifetime diagnosis of bipolar disorder, schizophrenia, or chronic psychotic
condition.
3. No current hazardous illicit drug or alcohol use.
4. No suicidal ideation or behavior requiring immediate attention.
5. Depression symptom severity: a Quick Inventory of Depressive Symptoms (QIDS) score
>11.
6. Taking an antidepressant medication for at least 6 weeks; prescribed by their primary
care provider.
7. Not in psychotherapy during the study period.
8. Have a PCP at our enrollment site.
9. If pregnant, less than 24 weeks gestation.
10. English speaking.
11. Aged 18 or older.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Major Depressive Disorder
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Intervention(s)
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Behavioral: Storytelling Video Intervention (sTVi)
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Primary Outcome(s)
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Client Satisfaction Questionnaire-8 (CSQ-8)
[Time Frame: 4 weeks]
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Secondary Outcome(s)
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Acceptance and Action Questionnaire-II (AAQ-II)
[Time Frame: 4 week]
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Quick Inventory of Depressive Symptomatology-Clinician Rating (QIDS-C)
[Time Frame: 4 weeks]
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Secondary ID(s)
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R34MH103568
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sTVi-1
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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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