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Effect of Vibratory Tendon Stimulation on Muscle Fatigue in the Acute Post-stroke Phase

Effect of Vibratory Tendon Stimulation on Muscle Fatigue in the Acute Post-stroke Phase : Vibramain1

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06296225
Acronym
VIBRAMAIN1
Enrollment
31
Registered
2024-03-06
Start date
2024-03-05
Completion date
2024-08-20
Last updated
2024-10-15

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

Conditions

Fatigue, Stroke, Stroke, Acute

Keywords

Stroke, vibration, Handgrip strength, Fatigue

Brief summary

It seems that prolonged vibratory stimulation of the anterior forearm in healthy subjects leads to fatigue of the muscles concerned, with a reduction in their strength. The aim of this study is to evaluate the impact of vibratory tendon stimulation on grip force fatigue during the acute post-stroke phase. The investigations will be carried out by a specialized physiotherapist from the neurology department. The experiment consists of three successive phases: * First : measurement of the maximum handgrip force before any vibratory stimulation and then after the three sessions of ten-minute vibration. * Second : Rest period * Third: control phase with measurement of the maximum grip force every ten minutes without vibration.

Interventions

DEVICEVibration

Grip strenght measurement will always be done in the same way : for each series, 3 measurements of maximum strength will be taken for each side. Participants will receive verbal encouragement. After initial both sides grip strength evaluation, all participant will first experiment the vibration situation using the device Vibramoov Physio (TechnoConcept, Manosque, France): the vibrations had a frequency of 100Hz, with an amplitude of 2mm, they will be applied to the anterior part of the forearm for 10 minutes, 3 times. At the end of each 10 minutes vibration session, handgrip strength will be assessed. * Participants then have a one-hour rest period. * Control situation: participants will have 4 series of grip strength measurements every 10 minutes. At the end of the 2 hours, the patient will be discharged from the study protocol.

Sponsors

Centre Hospitalier Régional d'Orléans
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Age:18 to 85 * Acute stroke (less than 7 days) * Paretic upper limb: 3 or 4 to the MRC score and able to obtain a value of at least 10 kilograms on the handgrip strength * Able to sign a consent form * Affiliated to a social insurance

Exclusion criteria

* Person under tutorship or curatorship, * Sleepiness * Pregnancy or breastfeeding woman

Design outcomes

Primary

MeasureTime frameDescription
Maximum handgrip strength measured by a digital dynamometer2 hoursHandgrip strength in kilograms

Secondary

MeasureTime frameDescription
Fatigue evolution2 hoursFatigue assessed with Borg Scale : Minimal score indicates no fatigue (Minimum : 0 - Maximum : 10)
Evolution of handgrip strength during the vibration session measured by a digital dynamometer30 minutesHandgrip strength in kilograms

Countries

France

Outcome results

None listed

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