CutaStim: Test-retest reliability of a superficial stimulation electrode for pain sensitivity measurements

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON28814

Enrollment

Registered

2017-05-03

Start date

2017-11-01

Completion date

Unknown

Last updated

2024-06-11

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

Conditions

Chronic pain

Interventions

None

Eligibility

Inclusion criteria

Inclusion criteria: Both groups: A signed, written informed consent; Age between 35 and 65. Pain patients: Enrolled in a pain rehabilitation program.

Exclusion criteria

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.

Design outcomes

Primary

Measure	Time frame
Electrical pain threshold (EPT) Current pain (NRS) Past pain (NRS average over last 7 days)	—

Secondary

Measure	Time frame
Central Sensitization symptoms: Central sensitization inventory (CSI) and central sensitization questionnaire (CSQ) Neuropathic pain symptoms: PainDETECT questionnaire (PD-Q)	—

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)