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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02134275
Other study ID # 10504
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 2015
Est. completion date November 2017

Study information

Verified date November 2018
Source Oregon Health and Science University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the benefits and feasibility of a whole body vibration (WBV) exercise program as a method of preventing weight gain in young adults.


Recruitment information / eligibility

Status Completed
Enrollment 176
Est. completion date November 2017
Est. primary completion date August 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. BMI that is between 22-29.9 kg/m2

2. History of being weight stable (± 2 kg) for three months prior to beginning the intervention

3. Not currently on a prescribed diet plan to lose weight and no plan to begin one

4. Not consistently engaged in physical activity that meets current public health recommendations of 150 minutes of moderate to vigorous physical activity in the previous 6 months

5. Currently enrolled as an undergraduate student in a degree-granting college or university

6. Planning to reside in the Portland Metro area for the duration of the study

Exclusion Criteria:

1. Health condition that would prevent participation in moderate intensity physical activity program.

2. For female participants, pregnancy or plans to become pregnant during the study period (source documentation: self-report on HHQ)

3. Currently smoking/tobacco products or initiation of smoking/tobacco during the study

4. Alcohol consumption exceeding 3 drinks per day or a total of 18 drinks per week

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Whole body vibration training
Each whole body vibration session will consist of a 20 min timed stand on the vibration platform where participants will stand with their knees in a slightly flexed position (120°) while the plate oscillates. The vibration frequency will be set at ranges between 20-40Hz and the amplitude set at 2mm displacement.
Control group
Participants in this group will be asked to not make any significant changes to their lifestyle behaviors, such as diet and exercise, for the duration of the study.

Locations

Country Name City State
United States OHSU School of Nursing Portland Oregon

Sponsors (1)

Lead Sponsor Collaborator
Oregon Health and Science University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in body composition (total body mass, fat-free mass, fat mass, regional fat mass, android/gynoid ratio and % body fat) across baseline, 3 and 6 months baseline, 3, 6 months
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