Bringing Exposure Therapy to Real-Life Context With Augmented Reality-Dogs (ARET)-Dogs
Specific Phobia, Animal
About this trial
This is an interventional treatment trial for Specific Phobia, Animal focused on measuring Exposure therapy, Technology, Telemedicine, Cynophobia
Eligibility Criteria
Inclusion Criteria:
Primary diagnosis of dog phobia, according to Diagnostic and Statistical Manual-5 (DSM-5) criteria
Willing and able to consent for involvement in the study
Exclusion Criteria:
People who refuse or are unable to consent to participate in the study
Current or previous diagnosis of psychotic disorder, schizophrenia, bipolar disorder, PTSD, mental retardation, active abuse of substances or meet criteria for substance use disorder in the past six months
Unstable behavior that, in the opinion of the investigator, would place the participant at increased risk or preclude the participant's full compliance with or completion of the study, e.g., significant Axis II disorder or suicidal behavior
Visual or auditory disabilities limiting ability to use the AR goggles
Current use of antidepressant medications, mood stabilizers, or benzodiazepines
History of seizures or a condition that would increase likelihood for seizures
Serious medical or neurological illness
Wards of the court
Sites / Locations
- Wayne State University Department of Psychiatry and Behavioral Neurosciences
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Intervention
Non-intervention
The experimental group will go through an exposure therapy session using an augmented reality headset device. The participant will work with the therapist, who will control the augmented reality paradigm and cater the exposure to the needs of the participant. The duration of the exposure will be as long as is needed to reduce anxiety regarding the feared object until self-reported subjective distress is low and stable.
The control group will not go through an exposure therapy session using an augmented reality headset device. This will be a no-intervention control group that can have some form of exposure therapy following the conclusion of the treatment/research period.