Depression Clinical Trial
Official title:
Web-based "Self-Help" Cognitive Behavioral Therapy for Symptoms of Mild-to-Moderate Anxiety and Depression in Adolescents and Young Adults With Chronic Illness
Verified date | April 2016 |
Source | Stanford University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
Symptoms of anxiety and depression are common in adolescents and young adults with chronic illnesses and are associated with decreased adherence to medical regimens. However, many young patients go untreated for anxiety and depression. The purpose of this study is to evaluate an online cognitive behavioral therapy (CBT) program in young adults with chronic illness. Prior research has shown online CBT to be effective in multiple other populations, but to the investigators' knowledge, this is the first study to examine web-based CBT for young adults with chronic illnesses.
Status | Completed |
Enrollment | 14 |
Est. completion date | August 2015 |
Est. primary completion date | May 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 15 Years to 25 Years |
Eligibility |
Inclusion Criteria: - Diagnosis of chronic illness - Language: English - Computer and Internet access - Symptoms of mild-moderate depression and/or anxiety Exclusion Criteria: - Existing mental health diagnosis - Psychoactive medications initiated in past 2 months - Severe depression - Suicidal ideation (refer to on-call psychiatrist and/or social worker for urgent intervention) or history of prior suicide attempt |
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Stanford University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Program satisfaction survey | Satisfaction with the web-based program will be assessed with a survey 3 months after enrollment in the study. | 3 months | No |
Primary | Program completion rates | Intervention completion rates will be used as a marker for acceptability of the intervention. | 6 weeks | No |
Secondary | Change in pre-and post-intervention score on measure of depression (PHQ-9) | Baseline and 3 months | No | |
Secondary | Change in pre-and post-intervention score on measure of anxiety (GAD-7) | Baseline and 3 months | No | |
Secondary | Change in pre-and post-intervention score on measure of quality of life (Peds-QL) | Baseline and 3 months | No | |
Secondary | Change in pre-and post-intervention score on measure of patient activation (PAM) | Baseline and 3 months | No |
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