Viewing Study NCT05823922



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Last Modification Date: 2024-10-26 @ 2:56 PM
Study NCT ID: NCT05823922
Status: RECRUITING
Last Update Posted: 2023-12-12
First Post: 2023-04-10

Brief Title: Mobile Cognitive Behavioral Therapy for Medical and Graduate Students
Sponsor: Weill Medical College of Cornell University
Organization: Weill Medical College of Cornell University

Study Overview

Official Title: Feasibility and Efficacy of Mobile Cognitive Behavioral Therapy for Medical and Graduate Students
Status: RECRUITING
Status Verified Date: 2023-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The study aims to assess and compare clinician-delivered cognitive behavior therapy CBT supplemented with MAYA a mobile cognitive behavioral therapy app program to clinician-delivered cognitive behavioral therapy alone The experimental group will be asked to use the mobile application at least two times per week for six weeks for at least 20 minutes on each of the two days in addition to the clinician-delivered CBT Participants will complete a weekly self-report assessment battery designed to assess anxiety and mood symptoms The investigators think that clinician-delivered CBT supplemented with MAYA will improve more effective at improving symptoms of anxiety and depression than clinician-delivered CBT alone
Detailed Description: Growing evidence suggests a need for anxiety and depression treatments that can be disseminated easily to young adults Many do not seek out treatment for reasons including lack of availability and high cost There is a growing need for accessible affordable research-supported treatments designed to increase the practice of skills and therefore improve treatment outcomes Graduate students use mobile devices frequently thus mobile app-based interventions may be particularly appealing to individuals in this age range with anxiety or depression who are unable to access more traditional psychotherapy administered in person by a therapist

The study aims to compare the efficacy and feasibility of clinician-delivered cognitive behavior therapy supplemented with the mobile app program to clinician- delivered cognitive behavioral therapy alone Young adults with anxiety andor depression will be randomized to clinician-delivered CBT active control group or to the clinician CBT mobile app intervention group In the active control group participants will participate in weekly clinician-delivered Cognitive Behavior Therapy In the intervention group participants will participate in weekly clinician-delivered Cognitive Behavior Therapy and use a mobile application for at least 20 minutes two times per week for six weeks

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None