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A symptom reduction study in body integrity identity disorder using augmented reality

A symptom reduction study in body integrity identity disorder using augmented reality - A symptom reduction study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON48656
Enrollment
2
Registered
2019-03-06
Start date
2019-04-02
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

A psychiatric disorder this is currently unclassified in DSM-V Anxiety depression

Interventions

Augmented reality.

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 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.;Inclusion criteria: -Men and women. -Age between 25-65. -Recently diagnosed with body integrity identity disorder. -Desire to amputate lower extremity/extremities (leg/legs).

Exclusion criteria

Exclusion criteria: - A desire for paralysis or other amputations that are not their lower extremities.

Design outcomes

Primary

MeasureTime frame
- Augmented reality task, the main study parameters consist of self-reports measured by a VAS and physiological recordings of heart rate and Skin Conductance level (SCL) measured by the VU-AMS. - Non-augmented reality task, the main study parameters consist of self-reports measured by a VAS and physiological recordings of heart rate and Skin Conductance level (SCL) measured by the VU-AMS.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)