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Objective physical arm activity assessment

Conditions
chronic obstructive pulmonary disease
10006436
Registration Number
NL-OMON34403
Lead Sponsor
Medisch Universitair Ziekenhuis Maastricht
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

Study A:
- Volunteers willing to participate
- Able to perform the standardized arm activity protocol (see document C1; study procedure)
- Fully competent;Study B:
- 10 COPD patients with lung hyperinflation, 10 COPD patients without lung hyperinflation and 10 healthy age matched volunteers
- Patients need to be clinically stable
- Able to walk (either with or without walking aids)
- Fully competent

Exclusion Criteria

Study A:
- Not willing to participate
- Unable to perform the standardized arm activity protocol (see study procedure);Study B:
- Not willing to participate
- Apparent neurological disorders.

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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