Ignite Creation Date:
2024-10-26 @ 3:42 PM
Last Modification Date:
2024-10-26 @ 3:42 PM
Study NCT ID:
NCT06628830
Status:
ENROLLING_BY_INVITATION
Last Update Posted:
None
First Post:
2024-10-03
Brief Title:
Efficacy of a Mobile Phone App for Depression and Anxiety in College Students
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Efficacy of a Mobile Phone Application for Early Intervention of Depression and Anxiety in Young College Students
Status:
ENROLLING_BY_INVITATION
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
VamosJuntxs
Brief Summary:
The goal of this clinical trial is to evaluate the efficacy of a mobile phone application for the early intervention of depression and anxiety among young university students in Chile The main question it aims to answer is
- Can a mobile app reduce depressive and anxious symptomatology in college students
Researchers will compare the intervention arm mobile app users to the control group receives psychoeducational material and mental health care resources to see if the app leads to significant improvements in depressive and anxious symptoms and well-being
Participants will
Be randomly assigned to either the intervention or control group
Use the mobile application which includes psychoeducational materials cognitive-behavioral therapy modules and periodic personalized feedback
Complete assessments at baseline post-intervention and 3 and 6 months after randomization using online tools such as the PHQ-9 for depressive symptoms and the GAD-7 for anxious symptoms
- Can a mobile app reduce depressive and anxious symptomatology in college students
Researchers will compare the intervention arm mobile app users to the control group receives psychoeducational material and mental health care resources to see if the app leads to significant improvements in depressive and anxious symptoms and well-being
Participants will
Be randomly assigned to either the intervention or control group
Use the mobile application which includes psychoeducational materials cognitive-behavioral therapy modules and periodic personalized feedback
Complete assessments at baseline post-intervention and 3 and 6 months after randomization using online tools such as the PHQ-9 for depressive symptoms and the GAD-7 for anxious symptoms
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None