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Feasibility study on the reduction of mechanically induced artefacts in surface EMG signals through the use of 3D-printed protective elements

Feasibility study on the reduction of mechanically induced artefacts in surface EMG signals through the use of 3D-printed protective elements

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00035777
Enrollment
12
Registered
2025-01-09
Start date
2025-01-13
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

mechanical artifacts in surface EMG signal acquisition

Interventions

Group 1: All participants undergo all test conditions. Each test subject is first tested without a box (NoBox) and then with a box (Box). In both conditions, defined disturbances (lateral and vertical

Sponsors

HAWKK HHG
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion Criteria: - Healthy adults (aged 18) with no known musculoskeletal disorders. - Ability to perform the required test movements (e.g., knee extensions, bending, lifting) without pain or discomfort. - No known neurological conditions affecting motor control or muscle activation patterns. - Ability to provide written informed consent and follow study instructions in English (or the language used in the study).

Exclusion criteria

Exclusion criteria: Exclusion Criteria: - Current or recent injury (within the past 6 months) to the lower limbs, trunk, or back that could impact muscle activation or movement patterns. - Any known allergy or skin sensitivity to adhesives or the materials used in the study (e.g., medical tape, electrode gels, TPU boxes). - Use of medications that significantly affect neuromuscular function (e.g., strong muscle relaxants, certain pain medications). - Inability or unwillingness to adhere to the study protocol or provide informed consent.

Design outcomes

Primary

MeasureTime frame
sEMG signal quality: Reduction of mechanical artefacts in surface EMG (quantified by comparison of RMS values) between conditions without box and with box under standardised perturbation conditions.

Secondary

MeasureTime frame
Physiological parameters of the skin: Measurement of skin temperature and skin moisture before and after each condition to assess possible influences of the boxes on the skin physiology and thus on the EMG signal quality.

Countries

Germany

Contacts

Public ContactImke Pitz

HAWK HHG

imke.pitz@hawk.de05515032-249

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026