A symptom reduction study in body integrity identity disorder using augmented reality
- Conditions
- A psychiatric disorder this is currently unclassified in DSM-VAnxietydepression
- Registration Number
- NL-OMON48656
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 2
The recruitment of participants takes place as follows. Practitioners at the department of Psychiatry will inform BIID patients that are currently or have previously been treated within our institution about our study. If someone is willing to participate in the study, we will personally visit with them at the Psychiatry department to inform them of the entire procedure. Moreover, they will receive an information letter by email that reviews all of the information again in detail in order to ensure that they have the opportunity to fully understand the procedure. After this, If they are still interested in participating, they will sign an informed consent and we will perform screening for inclusion and exclusion criteria.;
-Men and women.
-Age between 25-65.
-Recently diagnosed with body integrity identity disorder.
-Desire to amputate lower extremity/extremities (leg/legs).
- A desire for paralysis or other amputations that are not their lower extremities.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>- Augmented reality task, the main study parameters consist of self-reports<br /><br>measured by a VAS and physiological recordings of heart rate and Skin<br /><br>Conductance level (SCL) measured by the VU-AMS.<br /><br>- Non-augmented reality task, the main study parameters consist of self-reports<br /><br>measured by a VAS and physiological recordings of heart rate and Skin<br /><br>Conductance level (SCL) measured by the VU-AMS.</p><br>
- Secondary Outcome Measures
Name Time Method <p>N/A</p><br>