Whole-Body Vibration Training and Pilates Exercises for Healthy Women
Comparison of the Effects of Whole-Body Vibration Training and Pilates Exercises on Physical Fitness, Fatigue and Physical Self Perception in Healthy Women
1 other identifier
interventional
36
1 country
1
Brief Summary
This study aimed to compare the effects of whole-body vibration (WBV) training and Pilates exercises on physical fitness, fatigue, and physical self-perception in healthy women. This study was carried out on 36 healthy sedentary female subjects. Subjects were divided into three groups; Pilates training group, WBV training group, and control group. In the Pilates group, the exercises were performed with "Reformer®" for eight weeks, twice in a week, 45-min per day. In the WBV group, the training was given "Power Plate®" for eight weeks, twice in a week, and 30 minutes in a day. The control group did not receive any training.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2018
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 20, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 10, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
January 10, 2019
CompletedFirst Submitted
Initial submission to the registry
July 7, 2020
CompletedFirst Posted
Study publicly available on registry
July 29, 2020
CompletedJuly 29, 2020
July 1, 2020
5 months
July 7, 2020
July 24, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Body Composition Change
The body composition of the subjects was evaluated with bioelectrical impedance analysis (Tanita BC 601,Tanita Corp., Maeno-Cho, Tokyo, Japan). Body fat proportion was recorded as a percentage.
Pre-intervention and immediately after the intervention
Secondary Outcomes (13)
Body Mass Index
Pre-intervention and immediately after the intervention
Waist-hip ratio
Pre-intervention and immediately after the intervention
Aerobic capacity
Pre-intervention and immediately after the intervention
Flexibility
Pre-intervention and immediately after the intervention
Balance
Pre-intervention and immediately after the intervention
- +8 more secondary outcomes
Study Arms (3)
Pilates training group
EXPERIMENTALIn the Pilates group, the exercises were performed with "Reformer®" for eight weeks, twice in a week, one hour per day.
Whole-body vibration (WBV) group
EXPERIMENTALIn the WBV group, the training was given "Power Plate®" for eight weeks, twice in a week, and 30 minutes in a day.
Control group
NO INTERVENTIONThe control group did not receive any training.
Interventions
Pilates exercises are a combined exercise procedure including strengthening and stretching. Pilates exercises are performed with different equipment for example; therabands, mats, reformer, etc.
Whole-body vibration gives vibration to the body with a platform at different frequencies (Power-plate). The participant performed exercises on the platform.
Eligibility Criteria
You may qualify if:
- Individuals have not been exercising regularly in the last six months
- Physical activity level was between 600-3000 MET min/week (Metabolic equivalent minutes/week) according to the result of the "International Physical Activity Questionnaire"
- Bodyweight of less than 130 kg Individuals.
You may not qualify if:
- History of malignancy
- Pregnant individuals
- Musculoskeletal pain due to orthopedic or rheumatic diseases
- History of fractures in the past year
- Neurological disease (stroke, epilepsy, etc.)
- Chronic kidney or liver disease, cardiovascular diseases (cardiac arrhythmia, cardiac insufficiency, etc.)
- Imbalance due to peripheral vestibular disorder diagnosis (Benign paroxysmal positional vertigo, Meniere's disease, etc.)
- Individuals who not be able to tolerate vibration for more than five minutes were not included in the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Baskent University
Ankara, 06810, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Ozlem Yuruk, Assoc. Prof.
Baskent University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PT, PHD, Assoc Prof
Study Record Dates
First Submitted
July 7, 2020
First Posted
July 29, 2020
Study Start
August 20, 2018
Primary Completion
January 10, 2019
Study Completion
January 10, 2019
Last Updated
July 29, 2020
Record last verified: 2020-07