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Stimulus Phase Duration on Discomfort and Electrically Induced Torque of Quadriceps Femoris

The Influence of Stimulus Phase Duration on Discomfort and Electrically Induced Torque of Quadriceps Femoris

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01862393
Enrollment
38
Registered
2013-05-24
Start date
2008-08-31
Completion date
2008-12-31
Last updated
2016-09-01

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

Conditions

Pain Perception, Torque

Keywords

electrical stimulation, torque

Brief summary

This study aims to examine the variation in muscle torque and discomfort produced when electrically stimulating quadriceps femoris using pulsed current with three different phase durations in order to establish whether there are any advantages or disadvantages in varying the phase duration over the range examined.

Interventions

DEVICE400 microseconds

Neuromuscular electrical stimulation with stimulus phase duration of 400 microseconds

DEVICE700 microseconds

Neuromuscular electrical stimulation with stimulus phase duration of 700 microseconds

DEVICE1000 microseconds

Neuromuscular electrical stimulation with stimulus phase duration of 1000 microseconds

Sponsors

Universidade Cidade de Sao Paulo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* sedentary healthy university students.

Exclusion criteria

* history of knee surgery or injury, * musculoskeletal, cardiovascular or neurological disease including impaired sensation.

Design outcomes

Primary

MeasureTime frameDescription
TorqueDuring 4 seconds of electrical stimulationTorque will be measured using an isokinetic dynamometer. Torque will be registered in Newton meter \[N.m\]

Secondary

MeasureTime frameDescription
DiscomfortDuring 6 seconds of electrical stimulationDiscomfort will be measured using a 10 cm visual analogue scale (VAS) ranging from zero (no discomfort) to 10 (worst discomfort imaginable).

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026