Immediate Effects of Whole Body Vibration on Neuromuscular Performance of Quadriceps Femoris and Balance
Immediate Effects of Whole Body Vibration on Neuromuscular Performance of Quadriceps Femoris and Balance of Healthy Women: a Randomized Controlled Trial
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
RN
-
Natal, RN, Brazil, 59140-840
- Federal University of Rio Grande do Norte (UFRN)
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Female sex
- Healthy
- Engaging in physical activity involving lower limbs at least 3 times per week
- Exhibiting ankle, hip and knee joint integrity of the non-dominant limb
- No history of muscle or joint injuries in the assessed limb in the last 6 months, or neurological, visual and/or non-corrected auditory impairments
Exclusion Criteria:
- Auto-desistance
- Referring pain or discomfort during the procedures for collection
- Not perform assessment procedures correctly in order to make it impossible to capture the data.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
No Intervention: Control
The control group (No vibration) will hold an exercise protocol on the vibration platform, which is to stay on one foot on the non-dominant leg, with the knee held in 40 ° of flexion, hands together to the body and the trunk in the erect position.
Altogether, the participant will perform 11 sets of 30 seconds with a rest interval of 30 seconds between sets.
The knee angle will be monitored throughout the protocol by the second reviewer with a goniometer so that there is no change in it.
The vibrating platform will remain off throughout intervention.
|
|
|
Experimental: GE1
The GE1 (Vibration at 30 Hz) group will hold an exercise protocol on the vibration platform, which is to stay on one foot on the non-dominant leg, with the knee held in 40 ° of flexion, hands together to the body and the trunk in the erect position.
Altogether, the participant will perform 11 sets of 30 seconds with a rest interval of 30 seconds between sets.
The knee angle will be monitored throughout the protocol by the second reviewer with a goniometer so that there is no change in it.
During the sets the vibrating platform will be turned on at a vibration frequency of 30 Hz.
|
During the exercise protocol, the vibration platform will be turned on at a vibration frequency of 30 Hz.
|
|
Experimental: GE2
The GE1 (Vibration at 50 Hz) group will hold an exercise protocol on the vibration platform, which is to stay on one foot on the non-dominant leg, with the knee held in 40 ° of flexion, hands together to the body and the trunk in the erect position.
Altogether, the participant will perform 11 sets of 30 seconds with a rest interval of 30 seconds between sets.
The knee angle will be monitored throughout the protocol by the second reviewer with a goniometer so that there is no change in it.
During the sets the vibrating platform will be turned on at a vibration frequency of 50 Hz.
|
During the exercise protocol, the vibration platform will be turned on at a vibration frequency of 50 Hz.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle Performance measured through isokinetic dynamometry
Time Frame: Baseline, immediately after the intervention protocol
|
The muscle performance will be measured through isokinetic dynamometry and the variables analyzed will be peak torque normalized for body weight, mean power, total work and time to peak torque.
|
Baseline, immediately after the intervention protocol
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Proprioception measured through joint position sense in the isokinetic dynamometer
Time Frame: Baseline, immediately after the intervention protocol
|
The proprioception will be measured through joint position sense
|
Baseline, immediately after the intervention protocol
|
|
Muscle activation measured through surface electromyography
Time Frame: Baseline, immediately after the intervention protocol
|
Measured by surface electromyography
|
Baseline, immediately after the intervention protocol
|
|
Balance measured through baropodometry
Time Frame: Baseline, immediately after the intervention protocol
|
Measured by baropodometry
|
Baseline, immediately after the intervention protocol
|
Collaborators and Investigators
Sponsor
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
Other Study ID Numbers
- DTB2014
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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