VR during experimental pai
Recruiting
- Conditions
- Experimental pain - Experimentele pijnDistraction - AfleidingVirtual Reality
- Registration Number
- NL-OMON20465
- Lead Sponsor
- Martini Hospital Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 78
Inclusion Criteria
Healthy adults between 18 and 75 years old.
Exclusion Criteria
Limited sight or hearing, limited communication skills, acute or chronic pain, Phenomenon of Raynaud, cardiovascular disorders, hypertension, endocrine, metabolic and neurologic disorders, musculoskeletal disorders, epilepsy, psychiatric diagnoses, current injuries to the hands, use of medication, pregnancy, use of alcohol or drugs 24 hours before participation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1) the distraction technique is significantly associated with the VAS-pain score<br /><br>2) the distraction technique is significantly associated with the tolerance time
- Secondary Outcome Measures
Name Time Method 3) the executive functions and catastrophizing thoughts have a moderating role in the expected relation of the distraction technique and VAS pain score<br /><br>4) the VAS presence score predicts the VAS pain score<br /><br>5) the VAS presence score predicts the tolerance time<br /><br>6) the executive functions predict the VAS presence score<br /><br>7) the distraction technique predicts the VAS presence score