Virtual Reality Exposure Therapy Clinical Trial
— VRETOfficial title:
Cognitive Behavioral Therapy Based on Virtual Reality and Biofeedback Technology
The subjects were randomly assigned to VR treatment group and imaginary leak treatment group. In the VR treatment group, there were six VR exposure experiences, ranging from low to high levels of exposure, about 20 minutes each time, twice a week. During the course of treatment, physiological data such as skin electricity, skin temperature, heart rate and blood volume were measured, and the state of the subjects was evaluated more objectively. At the same time, every two minutes, the participants were asked the SUD value and recorded. AQ, ATHQ and BAT were recorded before treatment, after treatment and during the follow-up period of six months. The two groups were treated differently. n addition, at the beginning of this treatment program, an experimental study was added to understand the eye movement characteristics of patients with acrophobia. By viewing a group of high-altitude pictures, recording their eye movement characteristics and physiological feedback data, and scoring the anxiety level of each picture, and joining the normal control group, we can find a group of high-altitude pictures which can cause high-altitude fear in patients with high-altitude fear, and lay a foundation for future related research.
Status | Not yet recruiting |
Enrollment | 100 |
Est. completion date | October 1, 2020 |
Est. primary completion date | October 1, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 55 Years |
Eligibility |
Inclusion Criteria: 1.18-55 years old; 2.The anxiety scale in AQ scored more than 45.45 points ; 3.Meeting the DSM-IV criteria for specific phobia. Exclusion Criteria: 1. Other current or recent mental disorders, such as post-traumatic stress disorder; 2. Other physical diseases (such as heart disease and epilepsy) that may affect treatment; 3. Pregnancy or lactation; 4. No effect of psychotropic drugs or psychotherapy or prior exposure to heightphobia within 6 months (2013). |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Nanjing Medical University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | AQ | There were a total of 20 questions on the anxiety scale in the Acrophobia Questionnaire. Each topic scored 0-6 points. More than 45.45 points were included in the group to assess the differences in scores between the subjects before and after treatment. | 3 weeks |
Status | Clinical Trial | Phase | |
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