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Cognitive Behavioral Therapy
Computerized CBT for Depression (IDMPC Trial)
N/A
Waitlist Available
Led By Lucinda B Leung, MD MPH PhD
Research Sponsored by VA Office of Research and Development
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3-months
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing whether computerized cognitive behavioral therapy can help close the gap in psychotherapy access for Veterans with depression who receive care in primary care settings.
Who is the study for?
This trial is for Veterans with depression who can use a computer, internet, telephone, and email. They must be able to read English on-screen and score at least 10 on the PHQ-9 depression scale. It's not for those with conditions like dementia or terminal illness, high suicide risk or active suicidality, or serious mental illnesses like bipolar disorder or psychosis.
What is being tested?
The study tests if adding computerized cognitive behavioral therapy (cCBT) to VA's collaborative care improves access to psychotherapy for primary care patients with depression compared to usual care without cCBT.
What are the potential side effects?
Since this trial involves non-medical interventions such as cCBT and enhanced collaborative care, typical drug side effects are not expected. However, participants may experience discomfort discussing personal issues during therapy sessions.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3-months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3-months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Patient Health Questionnaire (PHQ-9)
Secondary study objectives
Mental Depression
Generalized Anxiety Disorder (GAD-7)
PROMIS Global Health
+2 moreOther study objectives
Treatment Engagement
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: cCBT Enhanced Collaborative CareExperimental Treatment1 Intervention
Participants in the intervention arm will receive computerized cognitive behavioral therapy (cCBT) supported by a depression care manager in addition to the usual care provided.
Group II: Usual CareActive Control1 Intervention
Participants in the usual care arm will receive the usual care provided as described below.
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Who is running the clinical trial?
VA Office of Research and DevelopmentLead Sponsor
1,658 Previous Clinical Trials
3,361,581 Total Patients Enrolled
78 Trials studying Depression
19,901 Patients Enrolled for Depression
Lucinda B Leung, MD MPH PhDPrincipal InvestigatorVA Greater Los Angeles Healthcare System, West Los Angeles, CA
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Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: cCBT Enhanced Collaborative Care
- Group 2: Usual Care
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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