Evaluation of an electronic device to objectively monitor energy expenditure, physical activity, unrest and autonomic nervous system function in patients admitted to the Intensive Care

Evaluation of an electronic device to objectively monitor energy expenditure, physical activity, unrest and autonomic nervous system function in patients admitted to the Intensive Care - Evaluation of a Sensewear device at the ICU

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON31133

Enrollment

Registered

2007-05-14

Start date

2007-03-01

Completion date

Unknown

Last updated

2024-05-13

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

Conditions

sedatie op ICU, nav mechanische beademing consciousness sedation

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 20 patients scheduled for elective cardiosurgery. 20 patients admitted to the ICU and are receiving sedation medication.

Exclusion criteria

Exclusion criteria: Patients treated with a pacemaker

Design outcomes

Primary

Measure	Time frame
For the study part where patients are undergoing elective cardiosurgery, the primary study parameter will be the function of the autonomic nervous system, which can be evaluated by measurements of the galvanic skin response (with the Sensewear device) and heart rate variability. For the study part where other ICu patients are studied, the primary study parameter will be the depth of sedation, which can be evaluated by measurements of BIS registration and acceleration (with the Sensewear device0.	—

Measure

Time frame

For the study part where patients are undergoing elective cardiosurgery, the primary study parameter will be the function of the autonomic nervous system, which can be evaluated by measurements of the galvanic skin response (with the Sensewear device) and heart rate variability. For the study part where other ICu patients are studied, the primary study parameter will be the depth of sedation, which can be evaluated by measurements of BIS registration and acceleration (with the Sensewear device0.

—

Secondary

Measure	Time frame
For both groups of patients, the secundary study parameters will be the other parameters of autonomic nervous system function as measured with the Sensewear device.	—

Countries

Netherlands

Outcome results