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Electrode usability during a multiday abdominal NMES program

Electrode usability during a multiday abdominal NMES program - VU-UT-01

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON45458
Enrollment
15
Registered
2017-04-11
Start date
2017-05-15
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

N/A

Interventions

The expiratory abdominal wall muscles will be stimulated for two times a day for a period of five consecutive days. This is done through similar protocols that are used in the study in ICU-patients.
electrode type
electrode-skin contact
healthy subjects
multiday neuromuscular electrical stimulation

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: - Informed consent - Age > 18 year - Healthy

Exclusion criteria

Exclusion criteria: - Recent abdominal surgery ( 35 kg/m2 - Dermatological disease that effects the abdominal wall - Pregnancy, breast feeding

Design outcomes

Primary

MeasureTime frame
Changes in physiological properties of the electrode-skin contact, during multiday NMES sessions. Primary endpoint: - Condition of the skin, measured in categories of dermal response.

Secondary

MeasureTime frame
Secondary parameters: - Series resistance (electrode + skin resistance) - Electrode adhesion - The difference in electrode resistance and capacitance before and after 5 days of use - Change in stimulus effect during multiday use of the same electrodes, measured as: - Maximal comfortable stimulation intensity - Sensitivity to stimulation - Abdominal muscle contraction, measured with ultrasound

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)