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Conditioned pain modulation in oarsmen compared to non-athletic controls - the ROW study

Conditioned pain modulation in oarsmen compared to non-athletic controls - the ROW study - ROW

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON47300
Enrollment
80
Registered
2019-01-24
Start date
2016-07-26
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

pijnverwerking pain modulation

Interventions

endogenous pain modulation
rowers

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Healthy male volunteers. The control cohorts (group 3 and 4 as listed above) is allowed to perform light to moderate exercise.

Exclusion criteria

Exclusion criteria: At least one of the following criteria: - Unable to understand study information or give oral and written informed consent; - Obesity (BMI > 30 kg/m2); - Pregnancy; - History of chronic alcohol or illicit drug use; - History of illness, condition or medication use that, in the opinion of the investigator, might interfere with optimal participation, or could confound the results of the study.

Design outcomes

Primary

MeasureTime frame
The CPM magnitude will be calculated by averaging the different tests, and comparing peak VAS values or area-under-the-curves to assess time- and conditioning-stimulus-related changes between groups.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)