- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02361203
Exercise and Virtual Reality Exposure Therapy for Acrophobia
February 1, 2016 updated by: Jolene Jacquart, University of Texas at Austin
The purpose of this study is to determine whether aerobic exercise can enhance the effects of exposure therapy treatment for fear of heights.
Study Overview
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Texas
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Austin, Texas, United States, 78712
- University of Texas at Austin
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 25 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Age 18 to 25
- Speaks English fluently
- Score of 80 or higher on the Acrophobia Questionnaire
- SUDS rating of 50 or higher on the Behavioral Avoidance Test or complete refusal to comply with instructions due to intensity of fear
- Passes the Physical Activity Readiness Questionnaire-Plus
Exclusion Criteria:
- Hearing or visually impaired
- Currently receiving exposure-based treatment for acrophobia
- Able to remain on floor 20 for 30 seconds during BAT with a SUDS rating < 50
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: No Exercise
|
|
Experimental: Exercise Pre
30 minutes of aerobic exercise before exposure therapy
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30 minutes of aerobic exercise on a treadmill at 80% of participant's heart rate reserve.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Fear scores
Time Frame: 7 (+/- 3) days after exposure therapy
|
Change in fear scores using subjective units of distress will be assessed.
|
7 (+/- 3) days after exposure therapy
|
Perceived threat likelihood scores
Time Frame: 7 (+/- 3) days after exposure therapy
|
Change in the perception of threat likelihood on a scale from 1-5 will be assessed.
|
7 (+/- 3) days after exposure therapy
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Skin conductance fluctuations
Time Frame: 7 (+/- 3) days after exposure therapy
|
Changes in skin conductance fluctuations will be assessed.
|
7 (+/- 3) days after exposure therapy
|
Heart rate fluctuations
Time Frame: 7 (+/- 3) days after exposure therapy
|
Heart rate fluctuations will be assessed.
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7 (+/- 3) days after exposure therapy
|
Acrophobia Severity
Time Frame: 14 (+/- 3) days after exposure therapy
|
Change in score on the Acrophobia Questionnaire
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14 (+/- 3) days after exposure therapy
|
Attitudes Toward Heights
Time Frame: 14 (+/- 3) days after exposure therapy
|
Change in score on the Attitudes Toward Heights Inventory
|
14 (+/- 3) days after exposure therapy
|
Clinical Global Improvement
Time Frame: 14 (+/- 3) days after exposure therapy
|
Change in score on the Clinical Global Improvement Scale
|
14 (+/- 3) days after exposure therapy
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jasper Smits, PhD, University of Texas at Austin
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2015
Primary Completion (Actual)
January 1, 2016
Study Completion (Actual)
January 1, 2016
Study Registration Dates
First Submitted
January 29, 2015
First Submitted That Met QC Criteria
February 5, 2015
First Posted (Estimate)
February 11, 2015
Study Record Updates
Last Update Posted (Estimate)
February 2, 2016
Last Update Submitted That Met QC Criteria
February 1, 2016
Last Verified
February 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- 2014-12-0037
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.
Clinical Trials on Fear of Heights
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Prof. Dominique de Quervain, MDCompleted
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Ruhr University of BochumCompletedFear of Spiders | Fear of HeightsGermany
-
University of Notre DameCompletedSpecific Phobia | Anxiety Disorder | Fear of Heights | AcrophobiaUnited States
-
National Institute of Mental Health, Czech RepublicRecruitingAnxiety Disorders | Specific Phobia | Fear of Heights | AcrophobiaCzechia
-
University of Nevada, RenoSuspendedAnxiety Disorders | Specific Phobia | Fear of Heights | AcrophobiaUnited States
-
New York State Psychiatric InstituteCompletedFear of Heights | Height Phobia
-
Ruhr University of BochumEnrolling by invitationFear of Heights | Specific Phobia, SituationalGermany
-
Dow University of Health SciencesCompletedVarying Heights of Power Arm During en Masse RetractionPakistan
-
Cairo UniversityUnknownImpact of Different Heel Heights on Spinal Configuration
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