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The ability to modulate the sensation of pain using augmented reality

The ability to modulate the sensation of pain using augmented reality - augmented reality pain modulation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON48970
Enrollment
16
Registered
2019-03-29
Start date
2019-06-27
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

human cognition physical discomfort visual processing

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 healthy participants via hand-outs and online flyers about our study. If someone is willing to participate in the study, we will email them to inform them of the entire procedure. This email will ensure that they have the opportunity to fully understand the procedure. If they are still interested in participating, they will sign an informed consent and we will perform screening for inclusion and exclusion criteria. Demographics and a clinician-related questionnaire (M.I.N.I) will be assessed to make sure that the individual can participate. If a participant meets any of the exclusion criteria, then they are excluded from participating in this study.;Inclusion criteria: - Men and women. - Age between 25-65. - No previous diagnosis of a mental disorder - No previous diagnosis of chronic pain

Exclusion criteria

Exclusion criteria: - A DSM-V diagnosis for any mental disorder - Diagnosed with having chronic pain

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)