Validation of CPM#1 compressibility in healthy volunteers in rest and after exercise

Recruiting

• Conditions: Chronic Exertional Compartment Syndrom; Lower Leg Pain; 10028302

• Registration Number: NL-OMON56011
• Lead Sponsor: Maxima Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 9 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 35

Inclusion Criteria

- >= 18 years
- Proficient in speaking and reading Dutch

Exclusion Criteria

- Presence or history of CECS
- History of surgery or other trauma which penetrated the fascia of the leg
- Other concurrent limb pathologies or anomalies amongst others:
- Peripheral arterial or venous disease
- Muscle disorders, diabetes mellitus, peripheral neuropathies
- Unable to exercise for 5-minutes
- Open wound at site of measurement

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>Inter-observer reliability of the compressibility measured with CPM#1 device</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>- To clinically validate the intra-observer reliability of compressibility<br /><br>measurements with the CPM#1 device during rest in healthy volunteers.<br /><br>- To investigate the effect of exercise on compressibility immediately, one<br /><br>minute, and five minutes after exercise in healthy volunteers.</p><br>