Research on Anxiety and Depression: Computer-Assisted Therapy
NCT ID: NCT02817438
Last Updated: 2019-03-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
136 participants
INTERVENTIONAL
2016-06-30
2018-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Online Intervention
Participants randomized to the online intervention arm will be given access to the Good Days Ahead program for 12 weeks.
Good Days Ahead
Good Days Ahead is a web-based program based on the principles of Cognitive Behavioral Therapy (CBT). It can be used to supplement traditional psychotherapy, or as a stand-alone intervention. There are 9 lessons that address Thinking Skills, Behavioral Skills, Schemas, and Coping Tools. Lessons include videos from expert therapists and a Practice Section in which patients complete forms for self-monitoring symptoms and challenging negative thoughts.
Waitlist
Participants randomized to the waitlist arm will wait for 12 weeks without doing an online intervention.
No interventions assigned to this group
Interventions
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Good Days Ahead
Good Days Ahead is a web-based program based on the principles of Cognitive Behavioral Therapy (CBT). It can be used to supplement traditional psychotherapy, or as a stand-alone intervention. There are 9 lessons that address Thinking Skills, Behavioral Skills, Schemas, and Coping Tools. Lessons include videos from expert therapists and a Practice Section in which patients complete forms for self-monitoring symptoms and challenging negative thoughts.
Eligibility Criteria
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Inclusion Criteria
* 18+ years of age
* Fluent and literate in English
* Can provide informed consent
* fMRI scanning eligibility, including no evidence of any form of metal embedded in the body (e.g., metal wires, nuts, bolts, screws, plates, sutures)
Exclusion Criteria
* Presence of suicidal ideations representing imminent risk
* General medical condition, disease, or neurological disorder that interferes with the assessments
* Mild traumatic brain injury (history of physical brain injury or blow to the head resulting in loss of consciousness greater than five minutes) and which could interfere with doing the assessments
* Severe impediment to vision, hearing and/or hand movement, likely to interfere with ability to complete the assessments
* Unable and/or unlikely to follow the study protocols
* Pregnant or breastfeeding
18 Years
ALL
Yes
Sponsors
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Stanford University
OTHER
Responsible Party
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Tali Manber Ball, PhD
Postdoctoral Scholar
Principal Investigators
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Tali Ball, PhD
Role: PRINCIPAL_INVESTIGATOR
Stanford University
Locations
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Stanford University
Stanford, California, United States
Countries
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Other Identifiers
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IRB-36790
Identifier Type: -
Identifier Source: org_study_id
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