Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04490577
Other study ID # KA18/268
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 20, 2018
Est. completion date January 10, 2019

Study information

Verified date July 2020
Source Baskent University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Description:

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 aged between 25-45 years. The study was conducted between August 2018-January 2019 in a health and physiotherapy clinic. This study was carried out on 36 healthy sedantary female subjects.

Before starting the study, the subjects were divided into three groups in a randomized manner using "Random Online Allocation Software" (www.Graphpad.com)

1. Group 1: Pilates training group

2. Group 2: WBV training group

3. Group 3: Control group

Pilates training group: The exercises were performed with "Reformer®" for eight weeks, twice in a week, 45-min per day. Warm-up and cool-down exercises were performed before and after the training.

WBV training group: The training was given "Power Plate®" for eight weeks, twice in a week, and 30 minutes in a day. Warm-up and cool-down exercises were performed before and after the training.

Control group: The control group did not receive any training.

The body composition of the subjects was evaluated with body mass index, waist-hip ratio and bioelectrical impedance analysis; functional capacity with Shuttle Run Test; core endurance with lateral bridge test, modified Biering-Sorensen test, trunk flexion test and prone bridge test and functional core strength with sit-ups and modified push-up tests. The stability of the core muscles was also measured with a pressure biofeedback instrument. The Sit and Reach test was used to assess flexibility and the Functional Reach Test was used for balance. Fatigue was evaluated with The Fatigue Severity Scale and physical self-perception was assessed with the Physical Self Perception Profile. The subjects were evaluated pre-intervention and immediately after the intervention.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date January 10, 2019
Est. primary completion date January 10, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 25 Years to 45 Years
Eligibility Inclusion Criteria:

- 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.

Exclusion Criteria:

- 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pilates exercises
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
Whole-body vibration gives vibration to the body with a platform at different frequencies (Power-plate). The participant performed exercises on the platform.

Locations

Country Name City State
Turkey Baskent University Ankara

Sponsors (1)

Lead Sponsor Collaborator
Baskent University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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 Body Mass Index The body composition of the subjects was evaluated with body mass index (BMI). The BMI is a person's weight in kilograms divided by the square of height in meters. A high BMI can be an indicator of high body fatness. Pre-intervention and immediately after the intervention
Secondary Waist-hip ratio The body composition of the subjects was also evaluated with waist-hip ratio. The waist to hip ratio measurement is calculated by dividing the measurement of your waist by your hip measurement. The score recorded as centimeter. Pre-intervention and immediately after the intervention
Secondary Aerobic capacity The aerobic capacity of the participants was evaluated with Shuttle-run test. Shuttle run test involve repetitive running back and forth, either over the same distance, or with changing distances. The shorter trial recorded as seconds. Pre-intervention and immediately after the intervention
Secondary Flexibility The sit and reach test used for flexibility. Sit and reach test measures measures the flexibility of the lower back and hamstring muscles.The score is recorded to the nearest centimeter as the distance reached by the hand. Pre-intervention and immediately after the intervention
Secondary Balance The balance was evaluated by Functional reach test. The test evaluated dynamic balance and limit of stability. This test measures the distance between the length of an outstretched arm in a maximal forward reach from a standing position,while maintaining a fixed base of support. The score recorded as centimeter. Higher scores indicate good level of balance. Pre-intervention and immediately after the intervention
Secondary Physical Self-Perception Physical self-perception was assessed with Physical Self Perception Profile. The questionnaire has four subdomain subscales designed to assess perceived bodily attractiveness, sports competence, physical strength, and physical conditioning were constructed along with a general physical self-worth subscale as the basis of the Physical Self-Perception Profile. Pre-intervention and immediately after the intervention
Secondary Fatigue Severity Scale The 9-item scale which measures the severity of fatigue and its effect on a person's activities and lifestyle. Each item consists of statements that are scored on a seven-point Likert type scale ranging from 1 ("strongly disagree") to 7 ("strongly agree"). The higher scores indicates severe fatigue. Pre-intervention and immediately after the intervention
Secondary Lateral Bridge test Lateral bridge test involves static, isometric contractions of the lateral muscles on each side of the trunk that stabilize the spine. The score recorded as second. Higher scores indicate good level of endurance. Pre-intervention and immediately after the intervention
Secondary Modified Biering-Sorensen test Modified Biering-Sorensen test measuring how many seconds the subject is able to keep the unsupported upper body (from the upper border of the iliac crest) horizontal, while placed prone with the buttocks and legs fixed to the couch by three wide canvas straps and the arms folded across the chest. The score recorded as second. Higher scores indicate good level of endurance. Pre-intervention and immediately after the intervention
Secondary Trunk flexion test Trunk flexion test involving a static, isometric contraction of the anterior muscles, stabilizing the spine until the individual exhibits fatigue and can no longer hold the assumed position. The score recorded as second. Higher scores indicate good level of endurance. Pre-intervention and immediately after the intervention
Secondary Prone bridge test The prone bridge test measures the muscular endurance of the abdominal muscles.The score recorded as second. Higher scores indicate good level of endurance. Pre-intervention and immediately after the intervention
Secondary Sit-ups test The sit-ups test is a measure the endurance of the abdominal and hip-flexor muscles. The aim of this test is to perform as many sit-ups as you can in two minutes. Pre-intervention and immediately after the intervention
Secondary Modified push-up test The modified push-up test was used to measure upper body strength endurance and trunk stability. This variation, which uses a modified technique with a clap behind the back while in the 'down' position and a touch from one hand to the other in the 'up' position.The total number of correctly completed push-ups were recorded. Pre-intervention and immediately after the intervention
See also
  Status Clinical Trial Phase
Completed NCT04959214 - The Effect Of Progressıve Relaxatıon Exercıses N/A
Recruiting NCT04984226 - Sodium Bicarbonate and Mitochondrial Energetics in Persons With CKD Phase 2
Completed NCT04531891 - Utility and Validity of a High-intensity, Intermittent Exercise Protocol N/A
Active, not recruiting NCT05006976 - A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study N/A
Completed NCT04960865 - Kinesio Taping and Calf Muscle Fatigue N/A
Completed NCT02948283 - Metformin Hydrochloride and Ritonavir in Treating Patients With Relapsed or Refractory Multiple Myeloma or Chronic Lymphocytic Leukemia Phase 1
Completed NCT06421233 - The Effect of Endorphin Massage Applied to Postpartum Women on Anxiety and Fatigue Levels N/A
Active, not recruiting NCT05344183 - Immediate and Short-term Effects of Low-level Laser N/A
Completed NCT04716049 - Effectiveness of Recovery Protocols in Elite Professional Young Soccer Players N/A
Completed NCT00060398 - Epoetin Alfa With or Without Dexamethasone in Treating Fatigue and Anemia in Patients With Hormone-Refractory Prostate Cancer Phase 3
Recruiting NCT05241405 - Evaluation of the Impact of Taking American Ginseng for 8 Weeks on Fatigue in Patients Treated for Localized Breast Cancer N/A
Active, not recruiting NCT06074627 - Radicle Energy2: A Study of Health and Wellness Products on Fatigue and Other Health Outcomes N/A
Completed NCT03943212 - The Effect of Blood Flow Rate on Dialysis Recovery Time in Patients Undergoing Maintenance Hemodialysis N/A
Recruiting NCT05567653 - Effects of Probiotics on Gut Microbiota, Endocannabinoid and Immune Activation and Symptoms of Fatigue in Dancers N/A
Active, not recruiting NCT05636696 - COMPANION: A Couple Intervention Targeting Cancer-related Fatigue N/A
Not yet recruiting NCT05863897 - e-COGRAT: A Blended eHealth Intervention for Fatigue Following Acquired Brain Injury N/A
Not yet recruiting NCT05002894 - Effect of Pilates Exercises On Fatigue In Post Menopausal Women N/A
Recruiting NCT04091789 - Sublingual Tablets With Cannabinoid Combinations for the Treatment of Dysmenorrhea Phase 2
Completed NCT02911649 - Reducing Sedentary Behaviour With Technology N/A
Completed NCT02321358 - Trial of a Behavior Change Intervention to Increase Aerobic and Resistance Exercise and Quality of Life in Older Prostate and Breast Cancer Survivors N/A