Objective physical arm activity assessment

Objective physical arm activity assessment - Objective physical arm activity assessment

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON34403

Enrollment

Registered

2010-12-20

Start date

2011-01-01

Completion date

Unknown

Last updated

2024-05-06

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

Conditions

chronic obstructive pulmonary disease

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

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

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.

Design outcomes

Primary

Measure	Time frame
Study A: • Orientation (Mly) and intensity (SMA) calculated from the accelerometer signals of the three acceleromters of the SensorSleeve (ACCwrist, ACCelbow and ACCshoulder). • Thresholds to define time spent in different activity categories (sec): 1) low orientation and low intensity, 2) low orientation and medium intensity, 3) low orientation and high intensity, 4) medium orientation and low intensity, 5) medium orientation and medium intensity, 6) medium orientation and high intensity, 7) high orientation and low intensity, 8) high orientation and medium intensity, 9) high orientation and high intensity. Time spend in different activity categories will be obtained from the protocol and calculated from the ACCwrist, ACCelbow and ACCshoulder. Study B: • Time spent in different activity categories measured using the CAM. • Burst characteristics of the m. biceps brachii, m. triceps brachii, m. deltoideus and m. trapezius pars descendens.	—

Measure

Time frame

Study A: • Orientation (Mly) and intensity (SMA) calculated from the accelerometer signals of the three acceleromters of the SensorSleeve (ACCwrist, ACCelbow and ACCshoulder). • Thresholds to define time spent in different activity categories (sec): 1) low orientation and low intensity, 2) low orientation and medium intensity, 3) low orientation and high intensity, 4) medium orientation and low intensity, 5) medium orientation and medium intensity, 6) medium orientation and high intensity, 7) high orientation and low intensity, 8) high orientation and medium intensity, 9) high orientation and high intensity. Time spend in different activity categories will be obtained from the protocol and calculated from the ACCwrist, ACCelbow and ACCshoulder. Study B: • Time spent in different activity categories measured using the CAM. • Burst characteristics of the m. biceps brachii, m. triceps brachii, m. deltoideus and m. trapezius pars descendens.

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Secondary

Measure	Time frame
Date of birth, gender, weight, body length.	—

Countries

Netherlands

Outcome results