Online Treatments for Mood and Anxiety Disorders in Primary Care
Completed · Phase 2/Phase 3
Conditions studied: Depression, Generalized Anxiety Disorder, Panic Disorder
In brief
Depression and anxiety are common in primary care practice and are associated with substantial reductions in health-related quality of life. This Project will test the comparative effectiveness of two on-line treatments for these conditions provided through the context of a Collaborative Care program: (1) moderated access to a proven-effective computerized cognitive behavioral therapy (CCBT) program; versus (2) moderated access to CCBT plus an Internet support group (CCBT+ISG). The Project will also compare the effectiveness of these treatments to PCPs' "usual care" for these conditions, and evaluate the adoption and maintenance of CCBT+ISG by practices following the conclusion of the trial to provide a greater understanding of how to best scale the delivery of these interventions into a variety of primary care settings.
Key facts
- Study ID
- NCT01482806
- Run by
- University of Pittsburgh
- People needed
- 700
- Starts
- 2012-02-01
- Expected to finish
- 2017-05-30
- Last updated by the study team
- 2020-08-05
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 18-75 Years of age.
- Current major depression, panic, and/or generalized anxiety disorder on PRIME-MD.
- At least a moderate level of mood and/or anxiety symptoms (PHQ-9 ≥ 10 or a GAD-7 ≥ 10).
- Not receiving treatment for a mood or anxiety disorder from a mental health specialist.
- Has a telephone, e-mail address, and reliable access to the Internet.
- Stable medical condition and life expectancy greater than one year.
You may not qualify if…
- Active suicidal ideation or psychotic disorder.
- History of bipolar disorder.
- Alcohol dependence or other substance abuse disorder within the past three months.
- Plans to leave present source of care over the following year.
- Non-English speaking, illiterate, or having a visual or auditory barrier limiting ability to participate in telephone assessments, interventions, or provide signed, informed consent.
Where it is running
- University of Pittsburgh Medical Center — Pittsburgh, Pennsylvania, United States
Full record on ClinicalTrials.gov
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