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Post-Fatigue Vibration: Impact on Grip and Reaction Time

Evaluation of Grip Strength and Reaction Time Following Induced Fatigue of the Wrist Flexors: The Acute Effects of Local Vibration

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06949566
Enrollment
42
Registered
2025-04-29
Start date
2025-05-08
Completion date
2025-06-26
Last updated
2025-07-11

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

Conditions

Muscle Fatigue

Keywords

Local Vibration, Upper Extremity Function, Wrist Flexors, Neuromuscular Performance

Brief summary

This study aims to investigate the acute effects of local vibration applied after induced fatigue of the wrist flexor muscles on grip strength and upper extremity reaction time.

Detailed description

This randomized controlled study will be conducted with a minimum of 42 participants who meet the inclusion and exclusion criteria. Participants will be randomly assigned to one of three groups: control, 50 Hz local vibration, or 100 Hz local vibration.

Interventions

OTHER100 Hz Local Vibration

Participants in this group will receive 100 Hz local vibration along the flexor carpi ulnaris muscle for a duration of 10 minutes.

OTHER50 Hz Local Vibration

Participants in this group will receive 50 Hz local vibration along the flexor carpi ulnaris muscle for a duration of 10 minutes.

OTHERSham Local Vibration

Participants in this group will receive sham vibration following the muscle fatigue protocol. The vibration device will be turned on but held near the muscle without making contact for 10 minutes. Participants will be informed that they are being treated with an electromagnetic vibration device.

Sponsors

Bitlis Eren University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Masking description

The evaluator and the researcher administering the plantar vibration intervention will be different. Patients will be blinded to their group assignment.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

1\. Female individuals aged 18-25

Exclusion criteria

1. Having an open wound in the area where local vibration is applied 2. A history of previous or current upper extremity injury 3. Use of anti-inflammatory drugs 4. Having a diagnosis of epilepsy

Design outcomes

Primary

MeasureTime frameDescription
Hand Grip Strength MeasurementChange in hand grip strength from baseline following intervention or restGrip strength will be assessed using a JAMAR® hydraulic hand dynamometer, which has five grip positions. The test will follow American Society of Hand Therapists guidelines, with the elbow at 90° flexion. Measurements will be taken on the dominant hand. Participants will sit with their head facing forward, shoulders slightly abducted (10-20°), elbows at 90°, and wrists and hands in a neutral position. Both upper extremities will remain relaxed, and feet will be flat on the floor. Fingers will be fully extended and adducted. Participants will be instructed not to allow their hands or forearms to touch the body. The dynamometer will be adjusted to fit the participant's hand size, typically set at the second handle position.
Upper Extremity Reaction Time MeasurementChange in upper extremity reaction time from baseline following following intervention or restUpper extremity reaction times will be recorded using the BlazePod system (Play Coyotta Ltd., Tel Aviv, Israel). Participants will begin the reaction time test while seated, with both hands placed on a table, palms facing downward, and elbows flexed at 90°, with hands positioned 40 cm apart. The BlazePod unit will be placed centrally, approximately 20 cm away from each hand. When the BlazePod lights up, participants will be instructed to respond as quickly as possible by tapping the light to turn it off. As the lights will activate randomly, participants will be required to react unpredictably and respond accordingly each time the light appears. The total test duration will be recorded at the end of the trial.

Other

MeasureTime frameDescription
Fatigue Perception and Relief Sensation After Vibration or RestChange in baseline fatigue perception and relief sensation following intervention or restTo evaluate the effects of local vibration on fatigue perception and relief sensation, participants will be asked to rate the intensity of these two parameters on a scale from 0 to 10 before and after the application. A score of 0 indicates the lowest intensity, while a score of 10 represents an unbearable level.
Post-Fatigue Fatigue RatingChange in baseline fatigue following muscle exhaustion protocolTo evaluate the perception of fatigue emerging after the fatigue protocol, participants will be asked to rate the intensity of their fatigue on a scale from 0 to 10. A score of 0 indicates no fatigue, while a score of 10 represents an unbearable level of fatigue.

Countries

Turkey (Türkiye)

Outcome results

None listed

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