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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04012762
Other study ID # Bitlis Eren University
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 15, 2019
Est. completion date July 8, 2019

Study information

Verified date July 2019
Source Okan University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date July 8, 2019
Est. primary completion date July 5, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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.

Locations

Country Name City State
Turkey Okan University Tuzla I?stanbul

Sponsors (1)

Lead Sponsor Collaborator
Tülay Çevik

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle Tone Tone assessments were made by MyotonPro Digital Palpation Device. 30 minute
Primary Muscle power The muscle power evaluation was made by Lafayette Manuel Muscle Testing System. 30 minute
Primary Flexibility Hamstring flexibility was evaluated with Sit and Reach Test. 30 minute
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