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Augmented Reality Exposure for Animal Phobia
N/A
Waitlist Available
Led By Arash Javanbakht, MD
Research Sponsored by Wayne State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Must not have
Serious medical or neurological illness
People who refuse or are unable to consent to participate in the study
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change in score from baseline to post treatment (immediately following the last exposure therapy session and at one-month follow-up)
Awards & highlights
No Placebo-Only Group
Summary
This trial uses augmented reality to help people who are afraid of dogs. Patients wear special glasses that show virtual dogs in their real surroundings. A therapist guides them through interactions with these virtual dogs to help reduce their fear.
Who is the study for?
This trial is for individuals who have a strong fear of dogs (cynophobia) as their main issue, confirmed by DSM-5 criteria. Participants must be willing and able to consent to the study. It's not suitable for those with unstable behavior, visual or auditory disabilities that affect AR goggle use, seizure history, under court care, on certain medications like antidepressants or mood stabilizers, or with serious medical conditions.
What is being tested?
The trial tests an augmented reality exposure therapy method for dog phobia using patented software and AR devices in a clinical setting. The patient undergoes guided exposure to virtual dogs in various forms while wearing AR goggles to reduce their fear response.
What are the potential side effects?
Since this intervention involves psychological therapy rather than medication, side effects may include temporary increases in anxiety during early treatment sessions as part of the normal process of exposure therapy.
Eligibility Criteria
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have a serious health or brain condition.
Select...
I am willing and able to give consent to participate in the study.
Select...
I have a history of seizures or a condition that increases my risk for seizures.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change in score on behavioral approach test from baseline to post treatment (immediately following the last exposure therapy session and at one-month follow-up)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change in score on behavioral approach test from baseline to post treatment (immediately following the last exposure therapy session and at one-month follow-up)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Behavioral Approach Test--Ability to confront phobia
Secondary study objectives
Cynophobia (fear of dogs) as measured by the Dog Phobia Questionnaire (DPQ)
Other study objectives
Autonomic Arousal
Credibility and expectancy of treatment efficacy as measured by the Credibility/Expectancy Questionnaire
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: InterventionExperimental Treatment1 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.
Group II: Non-interventionActive Control1 Intervention
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.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatment for animal phobia is exposure therapy, which works by gradually and systematically exposing patients to the feared animal in a controlled environment. This process helps patients confront and reduce their fear response through repeated exposure, leading to desensitization.
Augmented Reality Exposure Therapy (ARET) enhances this approach by using virtual objects to simulate real-life scenarios, allowing for diverse and controlled exposure that can be tailored to the patient's needs. This method is particularly beneficial as it provides a safe and flexible way to practice exposure outside the clinic, ensuring better generalization of safety learning to real-life situations.
For animal phobia patients, this means they can progressively overcome their fears in a structured and supportive manner, ultimately improving their quality of life.
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Who is running the clinical trial?
Wayne State UniversityLead Sponsor
314 Previous Clinical Trials
110,048 Total Patients Enrolled
Arash Javanbakht, MDPrincipal InvestigatorWayne State University
2 Previous Clinical Trials
154 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I have a serious health or brain condition.I am currently taking antidepressants, mood stabilizers, or benzodiazepines.I am willing and able to give consent to participate in the study.I have a history of seizures or a condition that increases my risk for seizures.I have been diagnosed with a severe fear of dogs.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Research Study Groups:
This trial has the following groups:- Group 1: Intervention
- Group 2: Non-intervention
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
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