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Behavioural Intervention
Common Elements Toolbox- Adult version (COMET-A) for Depression (COMET Trial)
N/A
Waitlist Available
Led By Akash Wasil
Research Sponsored by University of Pennsylvania
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Adult participants (at least 18 years old) will be eligible for this study
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediately after the intervention
Awards & highlights
COMET Trial Summary
Digital Mental Health and Wellness Intervention for Adults: A Randomized Control Trial of COMET
Eligible Conditions
- Depression
- Anxiety
COMET Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowCOMET Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 12 weeks post-intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 12 weeks post-intervention
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Ability to Cope with COVID-19
Change in Generalized Anxiety Disorder Screener-7 (GAD-7)
Change in Patient Health Questionnaire-9 (PHQ-9)
+5 moreCOMET Trial Design
3Treatment groups
Experimental Treatment
Active Control
Placebo Group
Group I: COMETExperimental Treatment1 Intervention
Participants receive modules focused on cognitive restructuring, gratitude, behavioral activation and self-compassion. Participants were randomized to receive 3 of the 4 possible modules: behavioral activation, cognitive restructuring, gratitude, and self-compassion.Participants in the intervention condition were randomized to receive descriptions of the four modules at the beginning of the intervention that were phrased to focus on building and improving strengths (positive) or reducing negative emotions and behaviors (negative).
Group II: WaitlistActive Control1 Intervention
Participants filled out all pre-test and post-test measures without having access to COMET of the active control exercises. Participants in this condition will receive access to COMET at the end of the study.
Group III: Self-Awareness ControlPlacebo Group1 Intervention
Participants learn about self-awareness through writing about memories, writing a short argumentative essay, and noticing objects in their surroundings.
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Who is running the clinical trial?
University of PennsylvaniaLead Sponsor
2,006 Previous Clinical Trials
42,880,552 Total Patients Enrolled
68 Trials studying Depression
26,908 Patients Enrolled for Depression
Robert J DeRubeis, PhDStudy DirectorUniversity of Pennsylvania
Akash WasilPrincipal InvestigatorUniversity of Pennsylvania
3 Previous Clinical Trials
1,252 Total Patients Enrolled
3 Trials studying Depression
1,252 Patients Enrolled for Depression
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