- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06004999
Effects of Whole Body Vibration in Pre-frail Individuals Over 65 Years of Age
Differential Effects of Whole-Body Vibration and Floor Exercises on Muscle Architecture, Functional Performance, and Well-Being in Pre-Frail Seniors: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Frailty is included in geriatric syndromes and is accepted as a precursor of other geriatric syndromes. The elderly who do not meet all the frailty criteria but are at risk are defined as "pre-frail". In many studies %50 of individuals aged 65 and over who appear healthy have been identified at an early stage and their progression to frailty can be reduced or prevented.
Proven treatment approaches for physical frailty include aerobic and resistive exercise. As a result of this study, it is predicted that whole body vibration may be an alternative treatment modality for "pre-frail " individuals who cannot do aerobic and resistive exercises or who are inconvenient to do these exercises.
In the literature, the effect of whole body vibration on muscle strength, balance, physical performance and spasticity in various age groups have been shown. There are no studies showing the effect of whole body vibration in pre-frail individuals and investigating the effect of whole body vibration on anterior thigh muscle thickness. In this study, pre-frail patients will be randomized into exercise groups. 6-week exercise programme is planned to be performed on whole body vibration platform for one group and on flat ground for the other group. The relationship between whole body vibration application and anterior thigh muscle thickness will be examined by measuring the anterior thigh muscle thickness of all participants via ultrasonography (USG). In addition, the relationship between whole body vibration application and body composition, physical performance, balance, kinesiophobia, mood, fatigue, quality of life and sleep will be examined.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Edirne, Turkey, 22030
- Trakya University Medical Faculty
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 65 years and older
- Those who agreed to participate in the study
- Groups that have the authority to understand and listen to the questions posed
- Having no regular exercise habits
Exclusion Criteria:
- Communication disorder that prevents storytelling and cooperation
- Serious neurological disease (central nervous system disorders such as paralysis, spinal cord injury, parkinsonism)
- Advanced cardiovascular disease (decongestive heart failure, recent myocardial infarction)
- Serious pulmonary disease (COPD exacerbation, acute pulmonary embolism)
- Physical disability such as lower extremity amputation, surgery
- Implant (pacemaker, artificial heart valve, stent, hip replacement, knee replacement)
- Pregnancy
- Epilepsy
- Having gallstones, kidney stones, bladder stones
- Acute inflammation, infection
- Acute or previous deep vein thrombosis
- Presence of a history of malignant disease
- History of fracture in the last 6 months
- History of lower extremity surgery in the last 12 months
- Having a regular exercise habit
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Vibration group
An exercise program organized by the researchers on the vibration platform will be applied to the pre-frail participants in the vibration group.
The exercises will be applied 5 days a week for 6 weeks.
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All patients will be pedaling for 5 minutes, followed by a warm-up phase with 5 minutes of stretching for the hamstring, gastrocnemius, soleus, and quadriceps muscles. Afterward, the following exercise program on the vibration platform will be applied to the 1st group.
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Active Comparator: Control group
An exercise program organized by the researchers (same exercise program as the vibration group) will be applied to the pre-frail participants in the control group on a flat surface.
The exercises will be applied 5 days a week for 6 weeks.
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All patients will be pedaling for 5 minutes, followed by a warm-up phase with 5 minutes of stretching for the hamstring, gastrocnemius, soleus, and quadriceps muscles. Afterward, the following exercise program will be applied to the group. The exercise program will be applied to the 2nd group (controls) on flat ground without a vibration platform.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Anterior thigh muscle thickness
Time Frame: Change from baseline anterior thigh muscle thickness at second, fourth and sixth weeks of intervention.
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Anterior thigh muscle thickness will be measured in centimeters by ultrasonography.
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Change from baseline anterior thigh muscle thickness at second, fourth and sixth weeks of intervention.
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Lower Extremity Muscle Strength
Time Frame: Change from baseline lower extremity muscle strength at sixth weeks of intervention
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The lower extremities will be evaluated by chair rise test ( also called chair stand test).
This test can be used as a proxy for strength of leg muscles (quadriceps muscle group).
The chair stand test measures the amount of time needed for a patient to rise five times from a seated position without using his or her arms; the timed chair stand test is a variation that counts how many times a patient can rise and sit in the chair over a 30-second interval.
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Change from baseline lower extremity muscle strength at sixth weeks of intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Hand grip strength
Time Frame: Change from baseline hand grip strength at sixth weeks of intervention
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Hand grip strength is a reliable measurement when standardised methods and calibrated equipment are used, even when there are different assessors or different brands of dynamometers.
Hand grip strength will be measured by Jamar Analogue Hand Dynamometer in kilograms.
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Change from baseline hand grip strength at sixth weeks of intervention
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Skeletal muscle mass index (SMI)
Time Frame: Change from baseline skeletal muscle mass index at sixth weeks of intervention
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Skeletal muscle mass index (SMI) will be measured in kg/m² by dividing the appendicular skeletal muscle mass (kg) by the square of the height (m) using bioelectrical impedance analysis (BIA).
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Change from baseline skeletal muscle mass index at sixth weeks of intervention
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Physical performance
Time Frame: Change from baseline physical performance at sixth weeks of intervention
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The Short Physical Performance Battery (SPPB) is used to determine physical performance.
The SPPB is a composite test that includes assessment of walking speed, balance test, and chair rise test.
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Change from baseline physical performance at sixth weeks of intervention
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Mobility
Time Frame: Change from baseline mobility at sixth weeks of intervention
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Mobility will be determined by the timed get-and-go test.
The test measures speed during many functional maneuvers such as standing up, walking, turning, and sitting.
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Change from baseline mobility at sixth weeks of intervention
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Physical activity
Time Frame: Change from baseline physical activity at sixth weeks of intervention
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Physical activity will be assessed using the International Physical Activity Questionnaire - short form (IPAQ).
It provides information about time spent walking, moderate- intensity activity, vigorous-intensity activity and sedentary activity.
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Change from baseline physical activity at sixth weeks of intervention
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Balance
Time Frame: Change from baseline balance at sixth weeks of intervention
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Balance will be scored by Berg balance test and Tinetti balance-gait tests.
Berg balance test scores balance between 0 to 56 in which higher score means better outcome.
Tinetti balance-gait test scores balance between 0 to 9 in which higher score means better outcome.
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Change from baseline balance at sixth weeks of intervention
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Kinesiophobia
Time Frame: Change from baseline kinesiophobia at sixth weeks of intervention
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Kinesiophobia will be determined by the Tampa Kinesiophobia Scale.
It consists of 17 questions including pain, injury, fear and avoidance parameters related to physical activities.
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Change from baseline kinesiophobia at sixth weeks of intervention
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Mood
Time Frame: Change from baseline mood at sixth weeks of intervention
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Depression will be assessed using Geriatric Depression Scale.
This scale consists of 30 questions.
A total score of 0-10 means no depression, 11-13 means likely depression, above 14 means definite depression.
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Change from baseline mood at sixth weeks of intervention
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Sleep quality
Time Frame: Change from baseline sleep quality at sixth weeks of intervention
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Sleep quality will be determined by The Pittsburgh Sleep Quality Index (PSQI).
The scale includes 7 components.
Every component is scored between 0 to 3. A total score above 5 is considered poor sleep quality.
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Change from baseline sleep quality at sixth weeks of intervention
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Fatigue
Time Frame: Change from baseline fatigue at sixth weeks of intervention
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Fatigue will be evaluated with the fatigue severity scale.
The scale includes 9 questions, each of which consists of a score scale of 1-7.
The scale determines the fatigue levels of the participants in the last 1 month.
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Change from baseline fatigue at sixth weeks of intervention
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Life quality
Time Frame: Change from baseline life quality at sixth weeks of intervention
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The 36-Item Short Form Survey (SF-36) is an outcome measure instrument that is often used, self-reported measure of health.
Life quality will be measured by SF-36.
In this test every subgroup is scored between 0 to 100 and higher score means better outcome.
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Change from baseline life quality at sixth weeks of intervention
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Filiz Tuna, Trakya University
Publications and helpful links
General Publications
- Kara M, Kaymak B, Ata AM, Ozkal O, Kara O, Baki A, Sengul Aycicek G, Topuz S, Karahan S, Soylu AR, Cakir B, Halil M, Ozcakar L. STAR-Sonographic Thigh Adjustment Ratio: A Golden Formula for the Diagnosis of Sarcopenia. Am J Phys Med Rehabil. 2020 Oct;99(10):902-908. doi: 10.1097/PHM.0000000000001439.
- Zhang L, Weng C, Liu M, Wang Q, Liu L, He Y. Effect of whole-body vibration exercise on mobility, balance ability and general health status in frail elderly patients: a pilot randomized controlled trial. Clin Rehabil. 2014 Jan;28(1):59-68. doi: 10.1177/0269215513492162. Epub 2013 Jul 17.
- Morley JE, Haren MT, Rolland Y, Kim MJ. Frailty. Med Clin North Am. 2006 Sep;90(5):837-47. doi: 10.1016/j.mcna.2006.05.019.
- Dent E, Martin FC, Bergman H, Woo J, Romero-Ortuno R, Walston JD. Management of frailty: opportunities, challenges, and future directions. Lancet. 2019 Oct 12;394(10206):1376-1386. doi: 10.1016/S0140-6736(19)31785-4.
- Stania M, Juras G, Slomka K, Chmielewska D, Krol P. The application of whole-body vibration in physiotherapy - A narrative review. Physiol Int. 2016 Jun 1;103(2):133-145. doi: 10.1556/036.103.2016.2.1.
- Lam FM, Lau RW, Chung RC, Pang MY. The effect of whole body vibration on balance, mobility and falls in older adults: a systematic review and meta-analysis. Maturitas. 2012 Jul;72(3):206-13. doi: 10.1016/j.maturitas.2012.04.009. Epub 2012 May 18.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- TÜTF-GOBEAEK 2022/335
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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