CutaStim: Test-retest reliability of a superficial stimulation electrode for pain sensitivity measurements
- Conditions
- Chronic pain
- Registration Number
- NL-OMON28814
- Lead Sponsor
- niversity of Twente, Biomedical Signals and Systems
- Brief Summary
one
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Both groups: A signed, written informed consent; Age between 35 and 65.
Pain patients: Enrolled in a pain rehabilitation program.
Exclusion Criteria
Both groups: Refusal during the study; Language problems; Skin problems; Unable to undergo eQST measurement; Diabetes; Implanted stimulation device;
Pregnancy
Pain patients: Average pain intensity of last 7 days of <2 on a NRS scale.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Electrical pain threshold (EPT)<br /><br>Current pain (NRS)<br /><br>Past pain (NRS average over last 7 days)<br>
- Secondary Outcome Measures
Name Time Method Central Sensitization symptoms: Central sensitization inventory (CSI) and central sensitization questionnaire (CSQ)<br>Neuropathic pain symptoms: PainDETECT questionnaire (PD-Q)