CT: Vibration Training and Muscles Properties

Sponsor
Tülay Çevik (Other)
Overall Status
Completed
CT.gov ID
NCT04012762
Collaborator
(none)
50
1
2
1.8
28.2

Study Details

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
  • Device: Whole body vibration training
N/A

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

Study Type:
Interventional
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 :
Jul 5, 2019
Actual Study Completion Date :
Jul 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 [30 minute]

    Tone assessments were made by MyotonPro Digital Palpation Device.

  2. Muscle power [30 minute]

    The muscle power evaluation was made by Lafayette Manuel Muscle Testing System.

  3. Flexibility [30 minute]

    Hamstring flexibility was evaluated with Sit and Reach Test.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Site City State Country Postal Code
1 Okan University Tuzla İ̇stanbul Turkey 34959

Sponsors and Collaborators

  • Tülay Çevik

Investigators

  • Principal Investigator: Emine Atıcı, Ph. D., Istanbul Okan University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Tülay Çevik, Principal Investigator, Okan University
ClinicalTrials.gov Identifier:
NCT04012762
Other Study ID Numbers:
  • Bitlis Eren University
First Posted:
Jul 9, 2019
Last Update Posted:
Jul 10, 2019
Last Verified:
Jul 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
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
Keywords provided by Tülay Çevik, Principal Investigator, Okan University

Study Results

No Results Posted as of Jul 10, 2019