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Influence of attentional modulation on pain-related evoked potentials (PREP) in healthy subjects

Influence of attentional modulation on pain-related evoked potentials (PREP) in healthy subjects

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00035963
Enrollment
40
Registered
2025-02-06
Start date
2019-11-15
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

healthy subjects

Interventions

Group 1: 1) Sequence of measurements 1. No moduation 2. Modulation through focus 3. Modulation through distraction 4. Modulation through increased expectancy 2) Increased expectancy with given more p

Sponsors

Neurologische Klinik, BG Universitätsklinikum Bergmannsheil gGmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: - no exclusion criteria present - declaration of consent

Exclusion criteria

Exclusion criteria: - Age 45 - Lack of informed consent - Average pain intensity in the last 4 weeks > 2 (NRS 0-10) - Current pain intensity > 0 (NRS 0-10) - Insufficient knowledge of German or other communication problems - Neuropathies, radiculopathies or nerve lesions - Painful condition of one or more extremities - Other neuropathic pain syndromes (e.g. polyneuropathy) - Treatment with topical local anaesthetics in the last 6 weeks - Treatment with topical capsaicin in the last 6 months - Epilepsy treated with anticonvulsants (carbamazepine, gabapentin, oxcarbazepine, pregabalin, valproate, etc.) - Psychiatric illness (e.g. severe depression, bipolar disorder, anxiety disorder) treated with antidepressants with proven effect on neuropathic pain (tricyclic AD, e.g. amitriptyline; SNRI, e.g. duloxetine, venlafaxine; SSRI, e.g. citalopram) - Psychiatric illness (e.g. severe depression, bipolar disorder, anxiety disorder) treated with anticonvulsants - Other severe systemic or focal CNS affection (e.g. stroke, spinal cord lesion, syringomyelia) - Other central or peripheral neurological diseases (e.g. Parkinson's disease, polyneuropathy, multiple sclerosis, dementia) - Peripheral arterial occlusive disease (up to stage Fontaine I) - Severe cognitive or psychiatric impairment - Cardiac pacemaker - Serious internal diseases - Diabetes mellitus - Existing long-term medication - Dependence on or abuse of substances (e.g. drugs, medication)

Design outcomes

Primary

MeasureTime frame
Change in N1P1-amplitudes, N1-latencies and evoked pain intensity of PREP under different attentional modulation compared to measurements without modulation

Secondary

MeasureTime frame
Comparison of N1P1-amplitudes, N1-latencies and evoked pain intensity of PREP of focus and distraction

Countries

Germany

Contacts

Public ContactOliver Höffken

Neurologische Klinik, BG Universitätsklinikum Bergmannsheil gGmbH

oliver.hoeffken@ruhr-universität-bochum.de+492343020

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026