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Evaluation of EEG-based pain perception in athletes in comparison to a healthy control group

Evaluation of EEG-based pain perception in athletes in comparison to a healthy control group - SPINE

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00022349
Enrollment
80
Registered
2020-07-24
Start date
2020-07-25
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

R52.2

Interventions

Group 1: Subjects in the group "healthy participants" will receive painful thermal, electrical and mechanical stimulation. Afterwards, we will apply a cold conditioning stimulus (Cold Pressor Test) to

Sponsors

Arbeitsgruppe Humane Schmerzmodelle Fraunhofer IME - Institutsteil TMP
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: To be included in the healthy control group, the subject must: -feel healthy and be physically and mentally fit -not be subject to one of the exclusion cirteria To be included in the group of athletes: -the subject must have a sport performance level that is on par with that of national junior athletes OR be competing on a national level in the second league in his or her form of sport OR must have a history of at least 2 years of competing in athletic competitions in his or her form of sport -the form of sport that the athlete is engaged in should be focused on putting weight on either the leg OR the whole body, such as rowing, triathlon, hockey, cycling, running

Exclusion criteria

Exclusion criteria: -no known pregnancy or ongoing nursing -no regular intake of pain medication -no intake of pain medication 24h prior to the study -no physical workload 24h prior to the study -no known sensibility disorder -no known severe illnesses that affect the quality of life (such as cardiovascular diseases, metabolic diseases, musculoskeletal disorders, depression) -no known introlerance to warming oinment

Design outcomes

Primary

MeasureTime frame
As this is an observational trial to some extent with the only exception being that the subject receives several well-tolerable painful stimuli, no mandatory primary outcome is defined. The aim of the study is to compare the magnitude and characteristics of painful EEG pattern after the study between both groups.

Countries

Germany

Contacts

Public ContactMalte Anders

Arbeitsgruppe Humane Schmerzmodelle, Fraunhofer IME - Institutsteil TMP

malte.anders@ime.fraunhofer.de069/6301-80255

Outcome results

None listed

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