Exploration of the effects of HFS-induced secondary hyperalgesia on the NDT-EP method
Recruiting
- Conditions
- one
- Registration Number
- NL-OMON25830
- Lead Sponsor
- niversity of Twente
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
(1) A signed, written informed consent; (2) Age between 16 and 40
Exclusion Criteria
(1) Participant refusal during the study; (2) Language problems; (3) Skin problems at site of stimulation or EEG recording; (4) Diabetes; (5) Implanted stimulation device; (6) Pregnancy; (7) Usage of analgesics within 24 hours before the experiment; (8) Excessive consumption of alcohol or drugs within 24 hours before the experiment; (9) Pain complaints at the time of the experiment; (10) (A medical history of) chronic pain
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method (1) Nociceptive Detection Thresholds (NDTs)<br>(2) EEG signals<br>(3) Numerical Rating Scale to mechanical punctate stimulation
- Secondary Outcome Measures
Name Time Method (1) Participant characteristics (Age, sex, handedness)<br>(2) Response time to stimuli<br>(3) Electrode-skin impedance