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

Completed

• Conditions: pijnverwerking; pain modulation

• Registration Number: NL-OMON47300
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2019-12-05
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 30

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

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.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The CPM magnitude will be calculated by averaging the different tests, and<br /><br>comparing peak VAS values or area-under-the-curves to assess time- and<br /><br>conditioning-stimulus-related changes between groups.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>na</p><br>