- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04831411
Comparison of Early Whole Body Vibration and Progressive Resistance Training in Fast-Track Total Knee Arthroplasty.
March 27, 2023 updated by: Gökhan Bayrak, Pamukkale University
Comparison of Early Whole Body Vibration and Progressive Resistance Training to Enhance Recovery After Fast-Track Total Knee Arthroplasty: A Randomized Comparative Study.
Patients who have undergone total knee arthroplasty (TKA) with Fast-Track recovery protocol at the Department of Orthopedics and Traumatology at the Local University Hospital and meet the inclusion and exclusion criteria will constitute the study sample.
The patients will be divided into 2 groups using the computerized randomization method in the post-operative 4th week; Whole Body Vibration Group and Progressive Resistance Exercise Group.
The first evaluation of the participants will be made at the end of the post-operative 4th week.
Final evaluations will be made at the end of the post-operative 10th week, following the 6-week training.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Patients who have undergone total knee arthroplasty (TKA) with Fast-Track recovery protocol at the Department of Orthopedics and Traumatology at the Local University Hospital and meet the inclusion and exclusion criteria will constitute the study sample.
The patients will be divided into 2 groups using the computerized randomization method in the post-operative 4th week; Whole Body Vibration Group and Progressive Resistance Exercise Group.
The first evaluation of the participants will be made at the end of the post-operative 4th week.
After 2 days and 6 weeks of training a week, final evaluations will be made at the end of the 10th postoperative week.
Evaluations will include measures of impairment in body functions and structures, activity limitation measures, balance assessment, and quality of life assessments.
Evaluations will be made by a blind researcher.
The study will be started with a total of 28 patients, including 14 participants in both groups.
The sample size was determined by performing a power analysis.
The purpose of the study will be explained to the patients by the researcher and the patients who agree to participate in the planned study will be included in the study.
Study Type
Interventional
Enrollment (Actual)
34
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Denizli, Turkey
- Gökhan Bayrak
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
50 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Undergoing unilateral TKA surgery due to knee OA,
- Being between the ages of 50-75,
- To be able to understand the verbal and written information given.
Exclusion Criteria:
- To undergo revision TKA surgery.
- Participating in any exercise or strengthening training within the last 3 months.
- Having undergone major surgery on the extremity to be operated on.
- Having a comorbid disease such as rheumatoid arthritis, cancer.
- Having a neurological disease that causes functional insufficiency.
- Having a diagnosed psychiatric disorder.
- Having received anaesthesia for any reason in the last 1 month.
- Regularly using hypnotics or anxiolytics.
- Having dementia.
- Having a hearing or vision impairment that cannot be corrected with a hearing aid or glasses.
- Being morbidly obese (Body mass index> 40 kg/m2).
- Having implanted pacemakers or defibrillators.
- Having dermatological problems affecting the thigh.
- Having a score above 3 in the American Society of Anesthesiologists classification score.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Whole Body Vibration
The training program will last 2 days a week and 6 weeks in total.
Each session includes a warm-up, progressive whole-body vibration training and a cooling exercise.
On the remaining days of the week, all patients will apply the standard exercise program, which includes simple home exercises, at home.
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The extremities of patients admitted to the operating room to be applied TKA will be determined using a safe surgical Fast-Track recovery protocol.
Patients will be operated by the same surgical team using the same technique.
Spinal anaesthesia or general anaesthesia will be applied to the patients according to the evaluations of the anesthesiologists.
Whole Body Vibration
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Active Comparator: Progressive Resistance Training
The training program will last 2 days a week and 6 weeks in total.
Each session includes a warm-up, progressive resistance training and a cooling exercise.
On the remaining days of the week, all patients will apply the standard exercise program, which includes simple home exercises, at home.
|
The extremities of patients admitted to the operating room to be applied TKA will be determined using a safe surgical Fast-Track recovery protocol.
Patients will be operated by the same surgical team using the same technique.
Spinal anaesthesia or general anaesthesia will be applied to the patients according to the evaluations of the anesthesiologists.
Progressive Resistance Training
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Balance
Time Frame: 6 weeks
|
Kinesthetic Ability Trainer® (KAT Model TS 650) will be used to evaluate balance.
Patients will use the lines on the platform to place their feet in the same place for each measurement.
Patients will be informed that the cursor on the system interface indicating the location of the pressure centre should be moved as little as possible and kept close to the centre.
The rates of pressure centre change will be recorded as a result of the balance score obtained after 30 seconds of measurements on bipedal feet.
Measurements will be applied in 3 repetitions and their average will be recorded and recorded in the study.
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6 weeks
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Quadriceps muscle strength
Time Frame: 6 weeks
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A handheld dynamometer (Commander Muscle Tester, JTech, USA) will be used for quadriceps muscle strength measurement.
Patients will be seated on the treatment table with their hips and knees in 90 ° flexion with their feet hanging down.
In this position, the hands will be on crossed shoulders and the use of bodyweight will be prevented.
During the measurements, verbal guidance will be given to the patients in order to achieve maximum effort.
Measurements will be made from the distal anterior face of the tibia with 3 consecutive maximum isometric contractions.
The average of the measurement values will be recorded as a score.
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6 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Pain assesment
Time Frame: 6 weeks
|
Pain will be assessed by the Visual Pain Scale (pain perceived during rest, sleep and walking).
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6 weeks
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Western Ontario and McMaster Universities Osteoarthritis Index score
Time Frame: 6 weeks
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Western Ontario and McMaster Universities Osteoarthritis Index score is a patient-reported questionnaire that evaluates pain, stiffness, and physical function in patients with hip and knee OA.
The index consists of 24 questions and the scores of the questions range from 0 (none) to 4 (very severe) and the results are evaluated over 100 points (minimum score:0 and the maximum score:100).
Higher scores indicate worst knee functions.
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6 weeks
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Quality of life measure
Time Frame: 6 weeks
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Short form-36 will be used for quality of life assessment.
SF-36 is a patient-reported questionnaire developed and made available to determine health-related quality of life.
SF-36 consists of 36 items that measure eight dimensions of physical function, social function, role limitations due to physical problems, role limitations due to emotional problems, mental health, energy/vitality, pain and general health perception.
The subscales assess health between 0 and 100, with 0 showing bad health and 100 showing better health.
Higher scores indicate better quality of life.
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6 weeks
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40 m fast-paced walk test
Time Frame: 6 weeks
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Patients will be asked to walk along the 10-meter track as fast as possible, turn around the cone at the finish, and complete the 40-meter total distance.
After the patient passed the baseline in the last stage, the time will be stopped and the total time will be recorded.
Lower walking distance indicates better walking capacity.
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6 weeks
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Sit-to-stand test
Time Frame: 6 weeks
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The patient will be seated in the middle of a chair with a height of standard 44 cm, with his back straight, arms crossed in front of his chest, and feet on the ground.
The patient will be asked to get up from the chair and sit down as much as the patient could for 30 seconds.
The exact number of starts will be made formed from the patient's score.
Higher scores indicate better overall strength.
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6 weeks
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Stair climbing test
Time Frame: 6 weeks
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The patient will be asked to climb and descend the 9-step 16-20 centimetre ladder as quickly but safely as possible.
The patient will be allowed to use a handrail or a walking aid, and the method used was recorded.
The test will start with the start command and the time stopped when the patient returned to the starting place.
The patient will be allowed to stop and rest when requested, but the duration will be continued.
The total time was recorded as a score.
Lower scores indicate better knee functions.
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6 weeks
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Timed up and go test
Time Frame: 6 weeks
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Timed up and go test (TUG) is a measurement that evaluates functional mobility, dynamic balance, fall risk and postural stability, which can be applied for different purposes in different age and patient groups.
The activities that make up the test evaluate the transition from sitting to standing position, walking, turning, and sitting again, which are necessary for functional mobility and dynamic balance.
The TUG test measures the time it takes an individual to get up from a standard chair with armrests and walk a distance of 3 meters, return from a designated or marked place, return to the chair, and sit down again.
Lower scores indicate better mobility and balance.
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6 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Gökhan Bayrak, Pamukkale University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Johnson AW, Myrer JW, Hunter I, Feland JB, Hopkins JT, Draper DO, Eggett D. Whole-body vibration strengthening compared to traditional strengthening during physical therapy in individuals with total knee arthroplasty. Physiother Theory Pract. 2010 May;26(4):215-25. doi: 10.3109/09593980902967196.
- Hsiao YH, Chien SH, Tu HP, Fu JC, Tsai ST, Chen YS, Chen YJ, Chen CH. Early Post-Operative Intervention of Whole-Body Vibration in Patients After Total Knee Arthroplasty: A Pilot Study. J Clin Med. 2019 Nov 7;8(11):1902. doi: 10.3390/jcm8111902.
- Bily W, Franz C, Trimmel L, Loefler S, Cvecka J, Zampieri S, Kasche W, Sarabon N, Zenz P, Kern H. Effects of Leg-Press Training With Moderate Vibration on Muscle Strength, Pain, and Function After Total Knee Arthroplasty: A Randomized Controlled Trial. Arch Phys Med Rehabil. 2016 Jun;97(6):857-65. doi: 10.1016/j.apmr.2015.12.015. Epub 2016 Jan 4.
- Wang P, Yang X, Yang Y, Yang L, Zhou Y, Liu C, Reinhardt JD, He C. Effects of whole body vibration on pain, stiffness and physical functions in patients with knee osteoarthritis: a systematic review and meta-analysis. Clin Rehabil. 2015 Oct;29(10):939-51. doi: 10.1177/0269215514564895. Epub 2014 Dec 18.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 4, 2021
Primary Completion (Actual)
July 8, 2022
Study Completion (Actual)
July 8, 2022
Study Registration Dates
First Submitted
April 1, 2021
First Submitted That Met QC Criteria
April 2, 2021
First Posted (Actual)
April 5, 2021
Study Record Updates
Last Update Posted (Actual)
March 28, 2023
Last Update Submitted That Met QC Criteria
March 27, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- WBV-PRE training after TKA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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