Evaluation of an 8-week Behavior Skills-based Virtual Reality Program for Adolescents With Depression. (MDD)
MDD
1 other identifier
interventional
10
1 country
1
Brief Summary
Evaluation of an 8-week Behavior Skills-based Virtual Reality Program for Adolescents With Depression.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2026
CompletedFirst Submitted
Initial submission to the registry
September 2, 2026
CompletedFirst Posted
Study publicly available on registry
September 8, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 1, 2027
September 8, 2026
September 1, 2026
3 months
September 2, 2026
September 2, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Virtual Reality use helps teens with depression
Using PHQ9 scores, does this program help improve their depression scores?
8 weeks
Virtual Reality use helps teens with anxiety
Using GAD7 scores, does this program help improve their anxiety scores?
8 weeks
Study Arms (1)
10 adolescents with diagnosis of depression
EXPERIMENTALThis is a single arm study for effectiveness. 10 adolescents will be enrolled in first study.
Interventions
We will use a combination of virtual reality experiences and educational experiences.
Eligibility Criteria
You may not qualify if:
- A patient that has been started on an antidepressant medication within the last 8 weeks.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Auroura Counseling
Washington, Iowa, 52353, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Lindsey Van Duyn, DO
Edward Via College of Osteopathic Medicine
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Masking Details
- The participants will be assigned a number which will identify their questionnaires responses.
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 2, 2026
First Posted
September 8, 2026
Study Start
September 1, 2026
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
January 1, 2027
Last Updated
September 8, 2026
Record last verified: 2026-09