Whole Body Vibration in Individuals Submitted to ACL
Immediate Effects of Whole Body Vibration on Neuromuscular Performance of Quadriceps Femoris in Individuals Submitted to Anterior Cruciate Ligament Reconstruction: A Randomized Clinical Trial
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Subjects between the 14th and 18th postoperatory week;
- Without pain or inflammatory signs in the joint assessed;
- Absence of labyrinthine and neurological disorders;
- Range of motion greater than 90o flexion and complete extension;
- No previous history of lower limb surgery before the lesion;
- Be performing Physical Therapy
Exclusion Criteria:
- Inability to understand and/or perform the required maneuvers;
- Presence of pain at the time of the tests;
- Complication preventing collection.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Vibration group
The vibration group (Vibration at 50 Hz) will hold an exercise protocol on the vibration platform (model Power Plate® pro5 ™), which is to stay on on affected limb, 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.
|
|
No Intervention: Control group
The control group (No vibration) will hold an exercise protocol on the vibration platform, which is to stay on affected limb, 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.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle Performance measured through isokinetic dynamometer
Time Frame: Change from baseline in muscle performance at one hour.
|
Measured through isokinetic dynamometer.
The variable analyzed will be: peak torque normalized by body weight (%).
|
Change from baseline in muscle performance at one hour.
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle activation measured through surface electromyography
Time Frame: Change from baseline in electromyographic activity at one hour.
|
Measured by surface electromyography.
The variable analyzed will be: RMS (Root Mean Square.
|
Change from baseline in electromyographic activity at one hour.
|
Collaborators and Investigators
Sponsor
Sponsor
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
Other Study ID Numbers
Other Study ID Numbers
- 07042915KA
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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