- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06468878
Virtual Reality Intervention for Fear of Heights
The Influence of Music on Response to Virtual Reality-Based Exposure for Acrophobia
Study Overview
Status
Conditions
Detailed Description
The goal of this clinical trial is to compare acrophobia (fear of heights) outcomes for VR exposure therapy in college students with elevated acrophobia when listening to music during exposure versus no music. The overarching aim of the current study is to determine how liked, non-lyrical background music will influence acrophobia outcomes after a brief exposure therapy session in VR.
The study involves three phases: (1) initial screening, (2) in-person assessment and a brief exposure intervention for a subset of participants with elevated acrophobia, and (3) a one-week follow-up assessment conducted online. Students who choose to participate and screen high on an acrophobia scale will be assigned to an experimental or control condition prior to undergoing VR based exposure therapy. Acrophobia outcomes are measured immediately post-intervention and one week later.
Researchers will compare participants in the music condition to participants in the non-music condition to see if acrophobia outcomes differ.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Michael Otto, PhD
- Phone Number: 617-353-9610
- Email: mwotto@bu.edu
Study Contact Backup
- Name: Laura J Long, PhD
- Phone Number: 617-358-4303
- Email: ljlong@bu.edu
Study Locations
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02215
- Recruiting
- Boston University
-
Principal Investigator:
- Michael W. Otto, Ph.D.
-
Contact:
- Laura J. Long, Ph.D.
- Phone Number: 617-358-4303
- Email: ljlong@bu.edu
-
Contact:
- Michael
- Phone Number: 617-353-9610
- Email: mwotto@bu.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Self-report of 18 years of age or older
- Current student at Boston University
- Ability to read English to provide informed consent
- Familiarity with a computer keyboard and mouse or a touch screen device (e.g. phone, tablet)
- For Phase 2: Acrophobia score of ≥ 45.45 on the Acrophobia Questionnaire (AQ) Anxiety Subscale
Exclusion Criteria:
- Previous participation (i.e. no participant may take the survey more than once).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Exposure Intervention with Non-Lyrical, Liked Background Music
Participants will be presented with a list of instrumental songs without lyrics from popular movies.
Participants will then rank the songs in order of those they would like to hear the most.
During VR heights exposure the participants' highest-ranked songs will be played in the background at a low volume.
|
VR exposure for acrophobia with background music.
|
|
Experimental: Exposure Intervention without Background Music
Participants will undergo VR heights exposure without background music.
|
VR exposure for acrophobia with no background music.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Acrophobia (Fear of Heights)
Time Frame: Comparison of pre-exposure scores to scores from the follow-up survey one week after exposure
|
Assessed using the Acrophobia Questionnaire (AQ) Anxiety Subscale
|
Comparison of pre-exposure scores to scores from the follow-up survey one week after exposure
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Valance
Time Frame: Comparison of pre-exposure scores to scores from the follow-up survey one week after exposure
|
Self-report measure of how participant feels about experiencing high-height environments.
|
Comparison of pre-exposure scores to scores from the follow-up survey one week after exposure
|
|
Height-Relevant Interpretations
Time Frame: Comparison of pre-exposure scores to scores from the follow-up survey one week after exposure
|
Assessed using the Heights Interpretation Questionnaire (HIQ)
|
Comparison of pre-exposure scores to scores from the follow-up survey one week after exposure
|
Collaborators and Investigators
Investigators
- Principal Investigator: Laura Long, PhD, Boston University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 7169E
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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