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The effect of electrical stimulation on muscle development in individuals with a spinal cord injury

Neuromuscular electrical stimulation and muscle protein synthesis in people with spinal cord injury - Neuromuscular electrical stimulation and muscle protein synthesis in people with spinal cord injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON58531
Enrollment
10
Registered
2025-06-10
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Spinal cord injury Damage to the spinal cord

Interventions

Participants will receive 5 days of twice-daily unilateral neuromuscular electrical stimulation (NMES).

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the followingcriteria:Chronic (> 1 year), motor complete SCI (ASIA Impairment Scale (AIS) A or B)Age between 18 and 70 yearsBMI between 18.8 and 30 kg/m2Having given ICIntact quadriceps muscles with visible muscle contractions on NMES 

Exclusion criteria

Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participationin this study:Flaccid paralysisExtreme quadriceps muscle spasticityA history of severe autonomic dysreflexiaDonated blood during 2 months prior to test day(Family) history of thrombosis Progressive diseaseInsufficient mastery of the Dutch language (speaking and reading)Intolerance to or contra-indication for neuromuscular electrical stimulation (cancer, pregnant, metal implants in stimulation area)Recent or current participation in an electrical stimulation-induced exercise program at the lower extremities or study (up to 1 month prior to this study)Participant in another study which might affect the results of the proposed studySevere psychiatric illness or disorders (to the discretion of the treating rehabilitation physician) Use of blood thinnersMedication related to muscle mass (e.g., anabolic steroids)

Design outcomes

Primary

MeasureTime frame
The primary outcome will be muscle protein synthesis rates.

Secondary

MeasureTime frame
Secondary outcomes include:Blood metabolic and inflammation markers such as glucose, insulin, cytokines (e.g., TNFa, MCP-1, IL-6, IL-10)To understand possible changes in muscle protein synthesis and breakdown, we will also analyze anabolic and proteolytic molecular pathways such as mTOR, FOXO, MuRF1, and MAFBx mRNA expression and signalingmTOR etc. (Western Blots)

Countries

Netherlands

Contacts

Public ContactJ.M. Stolwijk-Swüste

Universitair Medisch Centrum Utrecht

j.m.swuste@umcutrecht.nl088 75 588 31

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: May 1, 2026