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出境医 / 临床实验 / Vibration Training and Muscles Properties (CT)

Vibration Training and Muscles Properties (CT)

Study Description
Brief Summary:
Application dose standards have not yet been determined for Whole Body Vibration Training which is subject to studies with different frequencies and amplitudes. Our objective was to examine acute responses of two different vibration training doses on muscle tone, strength, and flexibility.

Condition or disease Intervention/treatment Phase
Muscle Relaxation Device: Whole body vibration training Not Applicable

Detailed Description:
Application dose standards have not yet been determined for Whole Body Vibration Training which is subject to studies with different frequencies and amplitudes. Our objective was to examine acute responses of two different vibration training doses on muscle tone, strength, and flexibility.
Study Design
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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 50 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Diagnostic
Official Title: The Acute Responses of Muscles Properties to the Different Whole Body Vibration Training
Actual Study Start Date : May 15, 2019
Actual Primary Completion Date : July 5, 2019
Actual Study Completion Date : July 8, 2019
Arms and Interventions
Arm Intervention/treatment
Active Comparator: Moderate-intensity group
WBVT application was 2-4 mm for vibration amplitude value and 25 Hz for training frequency in moderate-intensity group.
 Device: Whole body vibration training
Intermittent whole-body vibration exposure is a training method providing physical stimulation effect on skeletal muscles by increasing gravitational acceleration on the vibration platform.
Active Comparator: Vigorous-intensity group
WBVT application was 2-4 mm for vibration amplitude value and 40 Hz for training frequency in vigorous-intensity group.
 Device: Whole body vibration training
Intermittent whole-body vibration exposure is a training method providing physical stimulation effect on skeletal muscles by increasing gravitational acceleration on the vibration platform.
Outcome Measures
Primary Outcome Measures :
  1. Muscle Tone [ Time Frame: 30 minute ]
    Tone assessments were made by MyotonPro Digital Palpation Device.

  2. Muscle power [ Time Frame: 30 minute ]
    The muscle power evaluation was made by Lafayette Manuel Muscle Testing System.

  3. Flexibility [ Time Frame: 30 minute ]
    Hamstring flexibility was evaluated with Sit and Reach Test.


Eligibility Criteria
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Ages Eligible for Study:   18 Years to 35 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy and untrained participants.
  • Dominant side of the participants was recorded and only right dominant individuals were included.

Exclusion Criteria:

  • Participants with body weight over 120 kg.
  • Participants had lower extremity trauma and lower extremity movement restriction.
  • Participants who had any cardiovascular or neurological conditions, dizziness or vertigo
Contacts and Locations

Locations
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Turkey
Okan University
Tuzla, İ̇stanbul, Turkey, 34959
Sponsors and Collaborators
Tülay Çevik
Investigators
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Principal Investigator: Emine Atıcı, Ph. D. Istanbul Okan University
Tracking Information
First Submitted Date  ICMJE July 8, 2019
First Posted Date  ICMJE July 9, 2019
Last Update Posted Date July 10, 2019
Actual Study Start Date  ICMJE May 15, 2019
Actual Primary Completion Date July 5, 2019   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: July 8, 2019)
  • Muscle Tone [ Time Frame: 30 minute ]
    Tone assessments were made by MyotonPro Digital Palpation Device.
  • Muscle power [ Time Frame: 30 minute ]
    The muscle power evaluation was made by Lafayette Manuel Muscle Testing System.
  • Flexibility [ Time Frame: 30 minute ]
    Hamstring flexibility was evaluated with Sit and Reach Test.
Original Primary Outcome Measures  ICMJE Same as current
Change History No Changes Posted
Current Secondary Outcome Measures  ICMJE Not Provided
Original Secondary Outcome Measures  ICMJE Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Vibration Training and Muscles Properties
Official Title  ICMJE The Acute Responses of Muscles Properties to the Different Whole Body Vibration Training
Brief Summary Application dose standards have not yet been determined for Whole Body Vibration Training which is subject to studies with different frequencies and amplitudes. Our objective was to examine acute responses of two different vibration training doses on muscle tone, strength, and flexibility.
Detailed Description Application dose standards have not yet been determined for Whole Body Vibration Training which is subject to studies with different frequencies and amplitudes. Our objective was to examine acute responses of two different vibration training doses on muscle tone, strength, and flexibility.
Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Diagnostic
Condition  ICMJE Muscle Relaxation
Intervention  ICMJE Device: Whole body vibration training
Intermittent whole-body vibration exposure is a training method providing physical stimulation effect on skeletal muscles by increasing gravitational acceleration on the vibration platform.
Study Arms  ICMJE
  • Active Comparator: Moderate-intensity group
    WBVT application was 2-4 mm for vibration amplitude value and 25 Hz for training frequency in moderate-intensity group.
    Intervention: Device: Whole body vibration training
  • Active Comparator: Vigorous-intensity group
    WBVT application was 2-4 mm for vibration amplitude value and 40 Hz for training frequency in vigorous-intensity group.
    Intervention: Device: Whole body vibration training
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Completed
Actual Enrollment  ICMJE
 (submitted: July 8, 2019) 		50
Original Actual Enrollment  ICMJE Same as current
Actual Study Completion Date  ICMJE July 8, 2019
Actual Primary Completion Date July 5, 2019   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • Healthy and untrained participants.
  • Dominant side of the participants was recorded and only right dominant individuals were included.

Exclusion Criteria:

  • Participants with body weight over 120 kg.
  • Participants had lower extremity trauma and lower extremity movement restriction.
  • Participants who had any cardiovascular or neurological conditions, dizziness or vertigo
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 18 Years to 35 Years   (Adult)
Accepts Healthy Volunteers  ICMJE Yes
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE Turkey
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT04012762
Other Study ID Numbers  ICMJE Bitlis Eren University
Has Data Monitoring Committee No
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No
IPD Sharing Statement  ICMJE
Plan to Share IPD: No
Responsible Party Tülay Çevik, Okan University
Study Sponsor  ICMJE Tülay Çevik
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Principal Investigator: Emine Atıcı, Ph. D. Istanbul Okan University
PRS Account Okan University
Verification Date July 2019

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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