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Virtual reality & body experience in eating disorders

Virtual reality & body experience in eating disorders - VR in EDs

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42104
Enrollment
60
Registered
2014-10-01
Start date
2015-01-08
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

anorexia nervosa

Interventions

None listed

Sponsors

Universiteit Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients: Female, between 18 and 35 years of age, diagnosed with Anorexia Nervosa, physically non-disabled (i.e. able to perform the tasks during the experiment) Healthy controls: Female, between 18 and 35 years of age, BMI between 18.5 and 25, no current severe mental health problems, physically non-disables (i.e. able to perform tasks during the experiment).

Exclusion criteria

Exclusion criteria: Patients: Use of medication that may influence task performance due to sedative effects, drowsiness or (psycho)motor impairments, comorbid Borderline personality disorder or contact disorder, pregnancy. Healthy controls: Use of medication that may influence task performance due to sedative effects, drownsiness, or (psycho)motor impairments, pregnancy.

Design outcomes

Primary

MeasureTime frame
The primary study parameter in the current study is the error in size estimation of the size of the abdomen before and after providing multisensory input. By subtracting these two scores a difference score emerges. This allows for testing whether size estimation changed from pre to post multisensory input, and whether AN patients and healthy controls differ on this variable. In addition, participants will also estimate the size of control body parts (shoulders, hips, height), we do not expect any differences in size estimation error from pre to post multisensory stimulation.

Secondary

MeasureTime frame
The first secondary study parameter is again the difference in size estimation error from pre to post multisensory stimulation. However, not only group differences will be assessed, we will also investigate whether size estimation errors differ between synchronous and asynchronous multisensory stimulation. Based on our previous study we do not expect differences between providing multisensory input synchronously compared to asynchronously. The second secondary study parameter is the error in size estimation during the follow up measurement. This follow up error can be compared to pre and post size estimation errors. This will indicate whether within either group the change in body size experience after multisensory input is persistent over time.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)